Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework if you are London office based or homebased and live within the boundary of the M25) There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We re the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary. One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network. Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England. We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days annual leave, rising with service to 32.5 days, plus 8 Bank Holidays - NHS pension scheme, with around a 14% employer contribution - Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers - Cycle to work scheme - Internal reward scheme where you could win a voucher or two! - Equipment for homeworking Why this could be a great role for you If you re experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation. You ll play a pivotal role at the forefront of overseeing optimal healthcare across the nation. What s more, you ll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need: - Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations - Experience of handling confidential matters - Experience of keeping accurate document management logs - Experience of the liaison and co-ordination of requests as they arise - Experience of building effective relationships - The ability to work and deliver under pressure What you ll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations. Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews. You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst. Additionally, you will: - Support individual witnesses, alongside Engagement colleagues - Co-ordinate our agreed corporate position for statements - Liaise with the Director of Legal Services for legal support - Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management - Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application. We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation. So, if you d like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Apr 18, 2024
Contractor
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework if you are London office based or homebased and live within the boundary of the M25) There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We re the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary. One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network. Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England. We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days annual leave, rising with service to 32.5 days, plus 8 Bank Holidays - NHS pension scheme, with around a 14% employer contribution - Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers - Cycle to work scheme - Internal reward scheme where you could win a voucher or two! - Equipment for homeworking Why this could be a great role for you If you re experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation. You ll play a pivotal role at the forefront of overseeing optimal healthcare across the nation. What s more, you ll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need: - Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations - Experience of handling confidential matters - Experience of keeping accurate document management logs - Experience of the liaison and co-ordination of requests as they arise - Experience of building effective relationships - The ability to work and deliver under pressure What you ll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations. Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews. You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst. Additionally, you will: - Support individual witnesses, alongside Engagement colleagues - Co-ordinate our agreed corporate position for statements - Liaise with the Director of Legal Services for legal support - Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management - Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application. We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation. So, if you d like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
STRATEGIC RESOURCES EUROPEAN RECRUITMENT CONSULTANTS LTD
DATA ENGINEER - GIS (GIS ANALYST) Our client, a Major Oil and Gas Operator is seeking an experienced GIS Analyst. This will be supporting the offshore wind hub. It is a PAYE contract role initially until 30 November 2024 initially. MAIN ACTIVITIES: Deliver Geographical Information Service (GIS) for the Wind Hub using HQ technical specifications, procedures & standards, rules & processes, in order to meet their spatial data needs. Deliver GIS data requests to prepare, capture, search, transfer and QC data are fulfilled for the client or external parties to meet stakeholder needs within the scope and priorities of the service. Create, Publish and Manage map services for use in ArcGIS for Portal and ArcGIS Online (using ArcGIS Server and Image Server) Produce and manage complex cartographic documents using HQ technical specifications, procedures & standards, rules & processes for each offshore wind project. Co-build GIS studies such as offshore wind farm layouts, cable routings and site selection and undertake analyses for decision support Contribute to data acquisition operations in geomatics (e.g. topography, remote sensing), engineering (e.g. geophysical or geotechnical surveys),HSE surveys (e.g. environmental baseline or monitoring surveys) and consenting, from definition of needs to validation of deliverables. Execute appropriate geodetic calculations where required. Organize and provide GIS application support to end users or internal team. Follow up on the development, assessment and implementation of GIS and cartographic solutions and propose enhancement tools. Closely cooperate with HQ geospatial data information specialists for all GIS related matters. Closely follow, use & contribute to the development, drafting, updating and/or management of Technical Reference documents for this specialty. Collaborate, contribute and exchange know-how related to Geographical Information Systems. Promote and encourage the use of geographical information environment and data . SPECIFIC REQUIREMENTS: At least a BSc degree in Geographical Information Services or Computer Science disciplines with professional experience in development of energy and renewables projects. Technical skills in Geographical Information Systems, (ESRI software, inc ArcSDE and ArcGIS Server, FME, AGOL), geodesy and general knowledge of spatial data analysis techniques. Knowledge of other GIS software desirable, e.g. QGIS. Experience of Web GIS (ArcGIS for Portal/ArcGIS Enterprise & ArcGIS Online). Publishing and management of data, creation of web maps and web mapping applications Good knowledge of Geodesy Programming skills and aptitude in Python and SQL Experience of working within a Power BI based reporting environment. Knowledge of ETL tools (Safe FME) and scripting in Python, SQL. Organized, methodical and able to multi-task whilst working under tight deadlines
Apr 18, 2024
Contractor
DATA ENGINEER - GIS (GIS ANALYST) Our client, a Major Oil and Gas Operator is seeking an experienced GIS Analyst. This will be supporting the offshore wind hub. It is a PAYE contract role initially until 30 November 2024 initially. MAIN ACTIVITIES: Deliver Geographical Information Service (GIS) for the Wind Hub using HQ technical specifications, procedures & standards, rules & processes, in order to meet their spatial data needs. Deliver GIS data requests to prepare, capture, search, transfer and QC data are fulfilled for the client or external parties to meet stakeholder needs within the scope and priorities of the service. Create, Publish and Manage map services for use in ArcGIS for Portal and ArcGIS Online (using ArcGIS Server and Image Server) Produce and manage complex cartographic documents using HQ technical specifications, procedures & standards, rules & processes for each offshore wind project. Co-build GIS studies such as offshore wind farm layouts, cable routings and site selection and undertake analyses for decision support Contribute to data acquisition operations in geomatics (e.g. topography, remote sensing), engineering (e.g. geophysical or geotechnical surveys),HSE surveys (e.g. environmental baseline or monitoring surveys) and consenting, from definition of needs to validation of deliverables. Execute appropriate geodetic calculations where required. Organize and provide GIS application support to end users or internal team. Follow up on the development, assessment and implementation of GIS and cartographic solutions and propose enhancement tools. Closely cooperate with HQ geospatial data information specialists for all GIS related matters. Closely follow, use & contribute to the development, drafting, updating and/or management of Technical Reference documents for this specialty. Collaborate, contribute and exchange know-how related to Geographical Information Systems. Promote and encourage the use of geographical information environment and data . SPECIFIC REQUIREMENTS: At least a BSc degree in Geographical Information Services or Computer Science disciplines with professional experience in development of energy and renewables projects. Technical skills in Geographical Information Systems, (ESRI software, inc ArcSDE and ArcGIS Server, FME, AGOL), geodesy and general knowledge of spatial data analysis techniques. Knowledge of other GIS software desirable, e.g. QGIS. Experience of Web GIS (ArcGIS for Portal/ArcGIS Enterprise & ArcGIS Online). Publishing and management of data, creation of web maps and web mapping applications Good knowledge of Geodesy Programming skills and aptitude in Python and SQL Experience of working within a Power BI based reporting environment. Knowledge of ETL tools (Safe FME) and scripting in Python, SQL. Organized, methodical and able to multi-task whilst working under tight deadlines
Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analyst for the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site. This is a permanent role. Prospective candidates should have a science based education (GCSE) and an ability to carry out multiple tasks in a logical fashion. Previous laboratory experience is not essential, as full training will be given. This is a great entry level role. Principle Responsibilities: To undertake quality control analysis on liquid and dried extract, barley, malt and milled products. Follow work instructions in an organised, accurate and tidy manner in order to provide the analysis by the required time. The Candidate: A good team player and communicator. An awareness of Health & Safety principles. Self confidence and initiative to work with minimum supervision. A science/mathematics based education Hours of Work: Current requirements for this role are for 37.5 hours per week covering a 2 shift / 5 day shift pattern. Monday to Friday. Alternative 6.00 am to 2.00 pm and 1.30 pm to 9.30 pm. However, there is potential for the role to progress into a 2 shift / 7 day role. Training: We anticipate that the initial training period will be for a minimum of 3 months depending on the experience of the successful candidate. During the training period the hours of work will be Monday to Friday, 6.00 am to 2.00 pm with a 30-minute unpaid meal break.
Apr 16, 2024
Full time
Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analyst for the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site. This is a permanent role. Prospective candidates should have a science based education (GCSE) and an ability to carry out multiple tasks in a logical fashion. Previous laboratory experience is not essential, as full training will be given. This is a great entry level role. Principle Responsibilities: To undertake quality control analysis on liquid and dried extract, barley, malt and milled products. Follow work instructions in an organised, accurate and tidy manner in order to provide the analysis by the required time. The Candidate: A good team player and communicator. An awareness of Health & Safety principles. Self confidence and initiative to work with minimum supervision. A science/mathematics based education Hours of Work: Current requirements for this role are for 37.5 hours per week covering a 2 shift / 5 day shift pattern. Monday to Friday. Alternative 6.00 am to 2.00 pm and 1.30 pm to 9.30 pm. However, there is potential for the role to progress into a 2 shift / 7 day role. Training: We anticipate that the initial training period will be for a minimum of 3 months depending on the experience of the successful candidate. During the training period the hours of work will be Monday to Friday, 6.00 am to 2.00 pm with a 30-minute unpaid meal break.
An experienced Laboratory Analyst is required for Maternity cover - minimum 1 year for our client based in Aylesford. The successful candidate will work as part of the Quality Control Laboratory and will be responsible for the analysis of samples, chemical and consumable upkeep, ordering and inventory, waste and safety records, routine equipment maintenance, and managing daily work allocation. Other duties will include: Work as part of the team to prepare and coordinate daily activities in the laboratory relating to the analysis of samples in the laboratory. Maintain safety records and Material Safety Data Sheets General health & safety of laboratory within the laboratory. Maintain good hygiene and housekeeping at all times Maintain effective communication with other departments Check analytical results and issue reports Investigate failures and carry out corrective action Work with the other laboratory staff to participate in customer P-tests. Conducting vitamin and mineral analysis to achieve product release. Involved in analytical method development/transfer and validation plus report writing. Required to follow up on analytical issues and conduct trouble-shooting investigations Significant input in the authorship of SOPs Be able to take responsibility for the day-to-day running of the lab Have the opportunity to be involved in different internal projects You will have excellent communication and organisational skills and a high level of numeracy, accuracy and attention to detail. Also, to have the ability to plan ahead effectively. It is essential to be experienced in HPLC analysis and methodology, LCMS, UPC2 or ICP. Must have completed Science based A-Levels and a higher education at HND or Degree level will be an advantage. Must have at least 2-3 years of Laboratory experience in the Food/Pharmaceutical industry in a QC or R&D capacity.
Apr 16, 2024
Contractor
An experienced Laboratory Analyst is required for Maternity cover - minimum 1 year for our client based in Aylesford. The successful candidate will work as part of the Quality Control Laboratory and will be responsible for the analysis of samples, chemical and consumable upkeep, ordering and inventory, waste and safety records, routine equipment maintenance, and managing daily work allocation. Other duties will include: Work as part of the team to prepare and coordinate daily activities in the laboratory relating to the analysis of samples in the laboratory. Maintain safety records and Material Safety Data Sheets General health & safety of laboratory within the laboratory. Maintain good hygiene and housekeeping at all times Maintain effective communication with other departments Check analytical results and issue reports Investigate failures and carry out corrective action Work with the other laboratory staff to participate in customer P-tests. Conducting vitamin and mineral analysis to achieve product release. Involved in analytical method development/transfer and validation plus report writing. Required to follow up on analytical issues and conduct trouble-shooting investigations Significant input in the authorship of SOPs Be able to take responsibility for the day-to-day running of the lab Have the opportunity to be involved in different internal projects You will have excellent communication and organisational skills and a high level of numeracy, accuracy and attention to detail. Also, to have the ability to plan ahead effectively. It is essential to be experienced in HPLC analysis and methodology, LCMS, UPC2 or ICP. Must have completed Science based A-Levels and a higher education at HND or Degree level will be an advantage. Must have at least 2-3 years of Laboratory experience in the Food/Pharmaceutical industry in a QC or R&D capacity.
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework if you are London office based or homebased and live within the boundary of the M25) There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We re the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary. One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network. Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England. We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days annual leave, rising with service to 32.5 days, plus 8 Bank Holidays - NHS pension scheme, with around a 14% employer contribution - Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers - Cycle to work scheme - Internal reward scheme where you could win a voucher or two! - Equipment for homeworking Why this could be a great role for you If you re experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation. You ll play a pivotal role at the forefront of overseeing optimal healthcare across the nation. What s more, you ll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need: - Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations - Experience of handling confidential matters - Experience of keeping accurate document management logs - Experience of the liaison and co-ordination of requests as they arise - Experience of building effective relationships - The ability to work and deliver under pressure What you ll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations. Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews. You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst. Additionally, you will: - Support individual witnesses, alongside Engagement colleagues - Co-ordinate our agreed corporate position for statements - Liaise with the Director of Legal Services for legal support - Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management - Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application. We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation. So, if you d like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Apr 16, 2024
Contractor
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework if you are London office based or homebased and live within the boundary of the M25) There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We re the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary. One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network. Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England. We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days annual leave, rising with service to 32.5 days, plus 8 Bank Holidays - NHS pension scheme, with around a 14% employer contribution - Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers - Cycle to work scheme - Internal reward scheme where you could win a voucher or two! - Equipment for homeworking Why this could be a great role for you If you re experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation. You ll play a pivotal role at the forefront of overseeing optimal healthcare across the nation. What s more, you ll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need: - Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations - Experience of handling confidential matters - Experience of keeping accurate document management logs - Experience of the liaison and co-ordination of requests as they arise - Experience of building effective relationships - The ability to work and deliver under pressure What you ll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations. Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews. You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst. Additionally, you will: - Support individual witnesses, alongside Engagement colleagues - Co-ordinate our agreed corporate position for statements - Liaise with the Director of Legal Services for legal support - Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management - Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application. We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation. So, if you d like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Care Quality Commission
Newcastle Upon Tyne, Tyne And Wear
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework - if you are London office based or homebased and live within the boundary of the M25) - There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We're the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary.One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network.Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England.We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days' annual leave, rising with service to 32.5 days, plus 8 Bank Holidays- NHS pension scheme, with around a 14% employer contribution- Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers- Cycle to work scheme- Internal reward scheme where you could win a voucher or two!- Equipment for homeworking Why this could be a great role for you If you're experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation.You'll play a pivotal role at the forefront of overseeing optimal healthcare across the nation.What's more, you'll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need:- Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations- Experience of handling confidential matters- Experience of keeping accurate document management logs- Experience of the liaison and co-ordination of requests as they arise- Experience of building effective relationships- The ability to work and deliver under pressure What you'll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations.Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews.You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst.Additionally, you will: - Support individual witnesses, alongside Engagement colleagues- Co-ordinate our agreed corporate position for statements- Liaise with the Director of Legal Services for legal support- Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management- Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application.We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation.So, if you'd like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Apr 14, 2024
Full time
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework - if you are London office based or homebased and live within the boundary of the M25) - There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We're the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary.One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network.Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England.We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days' annual leave, rising with service to 32.5 days, plus 8 Bank Holidays- NHS pension scheme, with around a 14% employer contribution- Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers- Cycle to work scheme- Internal reward scheme where you could win a voucher or two!- Equipment for homeworking Why this could be a great role for you If you're experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation.You'll play a pivotal role at the forefront of overseeing optimal healthcare across the nation.What's more, you'll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need:- Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations- Experience of handling confidential matters- Experience of keeping accurate document management logs- Experience of the liaison and co-ordination of requests as they arise- Experience of building effective relationships- The ability to work and deliver under pressure What you'll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations.Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews.You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst.Additionally, you will: - Support individual witnesses, alongside Engagement colleagues- Co-ordinate our agreed corporate position for statements- Liaise with the Director of Legal Services for legal support- Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management- Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application.We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation.So, if you'd like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Highgrove Recruitment Group Limited
Stafford, Staffordshire
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Apr 12, 2024
Full time
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analyst for the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site. This is a permanent role. Prospective candidates should have a science based education (GCSE) and an ability to carry out multiple tasks in a logical fashion. Previous laboratory experience is not essential, as full training will be given. This is a great entry level role. Principle Responsibilities: To undertake quality control analysis on liquid and dried extract, barley, malt and milled products. Follow work instructions in an organised, accurate and tidy manner in order to provide the analysis by the required time. The Candidate: A good team player and communicator. An awareness of Health & Safety principles. Self confidence and initiative to work with minimum supervision. A science/mathematics based education Hours of Work: Current requirements for this role are for 37.5 hours per week covering a 2 shift / 5 day shift pattern. Monday to Friday. Alternative 6.00 am to 2.00 pm and 1.30 pm to 9.30 pm. However, there is potential for the role to progress into a 2 shift / 7 day role. Training: We anticipate that the initial training period will be for a minimum of 3 months depending on the experience of the successful candidate. During the training period the hours of work will be Monday to Friday, 6.00 am to 2.00 pm with a 30-minute unpaid meal break.
Apr 12, 2024
Full time
Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analyst for the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site. This is a permanent role. Prospective candidates should have a science based education (GCSE) and an ability to carry out multiple tasks in a logical fashion. Previous laboratory experience is not essential, as full training will be given. This is a great entry level role. Principle Responsibilities: To undertake quality control analysis on liquid and dried extract, barley, malt and milled products. Follow work instructions in an organised, accurate and tidy manner in order to provide the analysis by the required time. The Candidate: A good team player and communicator. An awareness of Health & Safety principles. Self confidence and initiative to work with minimum supervision. A science/mathematics based education Hours of Work: Current requirements for this role are for 37.5 hours per week covering a 2 shift / 5 day shift pattern. Monday to Friday. Alternative 6.00 am to 2.00 pm and 1.30 pm to 9.30 pm. However, there is potential for the role to progress into a 2 shift / 7 day role. Training: We anticipate that the initial training period will be for a minimum of 3 months depending on the experience of the successful candidate. During the training period the hours of work will be Monday to Friday, 6.00 am to 2.00 pm with a 30-minute unpaid meal break.
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Apr 12, 2024
Full time
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Business Process Analyst
Berkshire Healthcare Foundation Trust
The closing date is 27 August 2023
Apply for this job
Job summary
Intelligent Automation (RPA) Business Process Analyst, based in Reading, Berkshire
This is an exciting opportunity to join a newly funded growing Intelligent Automation Team delivering Robotic Process Automation across the Organisation.
This is a hybrid working role combining home working and the requirement to travel across the Trust on a regular basis to attend Programme and other meetings as necessary.
You will be supported with an extensive training programme to support your own learning to enhance your current skill set in order to be able to contribute to all aspects of the IA programme with additional focus on change management and transportation of automations across the various environments.
The role will contribute to the identification of opportunities, process mapping in fine detail identified tasks and contribute to the recommendations to make changes to automate routine and repetitive processes.
Main duties of the job
You daily work willinclude, working alongside others to
* Identify, manage process/automated change in the projects identified.
* Build collaborative relationships with teams, services, and individuals.
* Document processes in high detail.
* Support programme socialisation via various communication methods
About us
Berkshire Healthcare has a record of achievement and success that places us as one of the best performing Trusts in the country. We are rated 'Outstanding' by the CQC, we have a history of strong financial performance, and we have a highly skilled and engaged workforce. We aspire to be an outstanding organisation for everyone: our people, our patients, their families, and their carers.
Some of the benefits of joining our team:
* Salary ranging fromBand 6 £33706-£40588 per annum.
* Flexible working opportunities and a strong emphasis on your work, life balance
* Annual leave - 27 days for new starters, plus bank holidays. Increasing to 29 days after 5 years and 33 days after 10 years NHS service. Pro rata for part time staff.
* Excellent learning and development opportunities.
* Salary sacrifice scheme for a new car
* Generous maternity, paternity and adoption leave for eligible staff.
* Advanced IT enablement and support.
* Confidential telephone care service providing independent support and advice for staff.
* And so much more!
We are committed to equal opportunities and welcome applications from all sections of the community, regardless of any protected characteristics. Reasonable adjustments will be made for disabled applicants where required.
The Trust may close any vacancy prior to the advertised closing date due to the high level of responses we receive for some of our vacancies.
Person Specification
Education/Qualifications
Essential
* Educated to degree level OR equivalent experience
* Change Management qualification OR equivalent experience
Desirable
* Project Management qualification or equivalent experience
Training
Desirable
* Business Analysis or Benefits Change Management experience.
* PRINCE 2 or equivalent project management course
Previous Experience
Essential
* Minimum 3 years' experience working in a project/digital transformation environment involved in business change or equivalent experience.
* Extensive knowledge or experience of multiple/complex systems
* Fluency in the use of MS Office applications
* Experience of exercising judgment to solve operational problems where the answers are not apparent.
Desirable
* Experience of identifying and managing benefits
Additional Requirements
Essential
* Full Driving License - Car Driver/Car Owner or Willing to travel between sites as required.
* Ability to work within a busy team environment where frequent periods of concentration are required
* Physical effort - Setting up rooms, projectors, training PC's and other IT related equipment
* Emotional effort - Dealing with users, clinicians, and senior staff, developing relationships and solving conflicts.
* Frequent concentrated effort on complex data and information process on a PC
Aug 24, 2023
Permanent
Business Process Analyst
Berkshire Healthcare Foundation Trust
The closing date is 27 August 2023
Apply for this job
Job summary
Intelligent Automation (RPA) Business Process Analyst, based in Reading, Berkshire
This is an exciting opportunity to join a newly funded growing Intelligent Automation Team delivering Robotic Process Automation across the Organisation.
This is a hybrid working role combining home working and the requirement to travel across the Trust on a regular basis to attend Programme and other meetings as necessary.
You will be supported with an extensive training programme to support your own learning to enhance your current skill set in order to be able to contribute to all aspects of the IA programme with additional focus on change management and transportation of automations across the various environments.
The role will contribute to the identification of opportunities, process mapping in fine detail identified tasks and contribute to the recommendations to make changes to automate routine and repetitive processes.
Main duties of the job
You daily work willinclude, working alongside others to
* Identify, manage process/automated change in the projects identified.
* Build collaborative relationships with teams, services, and individuals.
* Document processes in high detail.
* Support programme socialisation via various communication methods
About us
Berkshire Healthcare has a record of achievement and success that places us as one of the best performing Trusts in the country. We are rated 'Outstanding' by the CQC, we have a history of strong financial performance, and we have a highly skilled and engaged workforce. We aspire to be an outstanding organisation for everyone: our people, our patients, their families, and their carers.
Some of the benefits of joining our team:
* Salary ranging fromBand 6 £33706-£40588 per annum.
* Flexible working opportunities and a strong emphasis on your work, life balance
* Annual leave - 27 days for new starters, plus bank holidays. Increasing to 29 days after 5 years and 33 days after 10 years NHS service. Pro rata for part time staff.
* Excellent learning and development opportunities.
* Salary sacrifice scheme for a new car
* Generous maternity, paternity and adoption leave for eligible staff.
* Advanced IT enablement and support.
* Confidential telephone care service providing independent support and advice for staff.
* And so much more!
We are committed to equal opportunities and welcome applications from all sections of the community, regardless of any protected characteristics. Reasonable adjustments will be made for disabled applicants where required.
The Trust may close any vacancy prior to the advertised closing date due to the high level of responses we receive for some of our vacancies.
Person Specification
Education/Qualifications
Essential
* Educated to degree level OR equivalent experience
* Change Management qualification OR equivalent experience
Desirable
* Project Management qualification or equivalent experience
Training
Desirable
* Business Analysis or Benefits Change Management experience.
* PRINCE 2 or equivalent project management course
Previous Experience
Essential
* Minimum 3 years' experience working in a project/digital transformation environment involved in business change or equivalent experience.
* Extensive knowledge or experience of multiple/complex systems
* Fluency in the use of MS Office applications
* Experience of exercising judgment to solve operational problems where the answers are not apparent.
Desirable
* Experience of identifying and managing benefits
Additional Requirements
Essential
* Full Driving License - Car Driver/Car Owner or Willing to travel between sites as required.
* Ability to work within a busy team environment where frequent periods of concentration are required
* Physical effort - Setting up rooms, projectors, training PC's and other IT related equipment
* Emotional effort - Dealing with users, clinicians, and senior staff, developing relationships and solving conflicts.
* Frequent concentrated effort on complex data and information process on a PC
What you will do: The Senior Clinical Data Analyst (SCDA) shall independently perform all clinical data cleaning activities on assigned FSP projects, commensurate with experience and/or project role. Further responsibilities shall include support on data processing activities and study level documents e.g. Protocol Deviation Specification, Data Validation specification, etc. The SCDA may act as a Data Management Lead where required. Key Accountabilities: Assume the ability to meet the requirements of a CDA III roIe with a high degree of proficiency and autonomy. Lead/Responsible for data cleaning and data review activities e.g. query management. Management of project timelines (including creation, review and tracking of plans). Review of protocols and EDC Screens if required. Support data processing activities from database setup to database lock, e.g. SAE reconciliation. Perform user acceptance testing on study database setups. Perform medical coding on small studies. Track and review CRFs. Support data entry where required. Perform and or support the setup of DM documents and ensure proper documentation e.g. CRF Completion Guidelines (CCG) Perform/lead functional QC activities and testing. Mentor project team members. Be a subject matter expert when needed. Ideal candidate will possess: Bachelor's degree and / or other medical qualifications. Understanding of Global Data Operations tasks, specifically within Data Management and Database Programming and relevant data standards. Sound awareness of relevant regulations, including ICH-GCP, 21CRF11. Experience in clinical research. Good interpersonal, verbal and written communication skills. Knowledge of medical terminology and awareness of coding dictionaries (e.g.MedDRA & WHODRUG). Good knowledge of EDC systems (e.g. DataLabs, Rave.) Good knowledge of electronic source data capture systems (e.g. ClinBase). Good knowledge of all DB set-up activities including but not limited to Database Configuration. Specifications, Data Validation. Ability to work in team environment. Good analytical skills and attention to detail. Effective time management to meet daily metrics or team objectives, completion of assigned tasks in a timely manner. Basic knowledge of SAS.
Sep 22, 2022
Full time
What you will do: The Senior Clinical Data Analyst (SCDA) shall independently perform all clinical data cleaning activities on assigned FSP projects, commensurate with experience and/or project role. Further responsibilities shall include support on data processing activities and study level documents e.g. Protocol Deviation Specification, Data Validation specification, etc. The SCDA may act as a Data Management Lead where required. Key Accountabilities: Assume the ability to meet the requirements of a CDA III roIe with a high degree of proficiency and autonomy. Lead/Responsible for data cleaning and data review activities e.g. query management. Management of project timelines (including creation, review and tracking of plans). Review of protocols and EDC Screens if required. Support data processing activities from database setup to database lock, e.g. SAE reconciliation. Perform user acceptance testing on study database setups. Perform medical coding on small studies. Track and review CRFs. Support data entry where required. Perform and or support the setup of DM documents and ensure proper documentation e.g. CRF Completion Guidelines (CCG) Perform/lead functional QC activities and testing. Mentor project team members. Be a subject matter expert when needed. Ideal candidate will possess: Bachelor's degree and / or other medical qualifications. Understanding of Global Data Operations tasks, specifically within Data Management and Database Programming and relevant data standards. Sound awareness of relevant regulations, including ICH-GCP, 21CRF11. Experience in clinical research. Good interpersonal, verbal and written communication skills. Knowledge of medical terminology and awareness of coding dictionaries (e.g.MedDRA & WHODRUG). Good knowledge of EDC systems (e.g. DataLabs, Rave.) Good knowledge of electronic source data capture systems (e.g. ClinBase). Good knowledge of all DB set-up activities including but not limited to Database Configuration. Specifications, Data Validation. Ability to work in team environment. Good analytical skills and attention to detail. Effective time management to meet daily metrics or team objectives, completion of assigned tasks in a timely manner. Basic knowledge of SAS.
Proclinical are recruiting a QC Scientist (Stability) for a biotech establishment. This role is on a permanent basis and is located in Abingdon. The client is focused on revolutionising solutions for cancer. Responsibilities: Accountable for the protocol and document production of assays transfers linked to QC tests using practices such as ELISA, gel electrophoresis, bioassay's spectroscopy, PCR, etc. Uphold QC systems linked to in-process, final drug product and stability sample. Evaluate testing data of other analysts. Supervise sampling and storage of QC samples and uphold retain inventory. Conduct QC testing of raw resources, in-process, water and product samples adhering to SOPs. You will engage within internal as well as cross functionally to communicate QC needs. Organise shipping samples to Milton Park and contract testing labs. Form, review and uphold processes for QC testing. Support the upkeep of QC lab and equipment. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a chemistry/biochemistry/microbiology or a similar science discipline. At least 3 - 5 years of experience with GLP/GMP within a pertinent work setting. Computer literacy in MS Word, Excel, etc. Works well within a team setting. Communication skills both verbally and in writing. An organised individual. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting a QC Scientist (Stability) for a biotech establishment. This role is on a permanent basis and is located in Abingdon. The client is focused on revolutionising solutions for cancer. Responsibilities: Accountable for the protocol and document production of assays transfers linked to QC tests using practices such as ELISA, gel electrophoresis, bioassay's spectroscopy, PCR, etc. Uphold QC systems linked to in-process, final drug product and stability sample. Evaluate testing data of other analysts. Supervise sampling and storage of QC samples and uphold retain inventory. Conduct QC testing of raw resources, in-process, water and product samples adhering to SOPs. You will engage within internal as well as cross functionally to communicate QC needs. Organise shipping samples to Milton Park and contract testing labs. Form, review and uphold processes for QC testing. Support the upkeep of QC lab and equipment. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a chemistry/biochemistry/microbiology or a similar science discipline. At least 3 - 5 years of experience with GLP/GMP within a pertinent work setting. Computer literacy in MS Word, Excel, etc. Works well within a team setting. Communication skills both verbally and in writing. An organised individual. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Fantastic opportunity for an experienced Business Development Manager seeking a new challenge! Our company is well established within the food technology industry and are able to offer a wide a range of testing services such as raw materials, nutrition, safety, packaging, QA/QC, toxins and many other services. Due to demand, they now require a Business Development Manager to secure new business in Scotland to the North East of England. This is proactive business development position where you will search and identify new opportunities through a variety of methods such as networking events, LinkedIn, responding to incoming enquires and previous leads, etc. To be considered for this role you must have: Good knowledge or experience of food or beverage manufacture/testing (gained from sales or lab experience) A proven record in Business Development Degree in a relevant subject - Chemistry/Nutrition/Biochemistry etc Knowledge and experience working with CRM systems Team player mindset, excellent interpersonal skills Above all an energetic and a desire succeed attitude! The position comes with a company car, phone, laptop etc + 10% bonus and training related to services on offer. Apply to VRS now to be considered for this exciting new opportunity! Keywords: food testing, water testing, food & beverage, Sales, service sales, food and nutritional services, food safety analysis, business development, commercial manager, acquisitions, new business, strategic, scientific sales, Analyst, chromatography, wet chemistry, analytical, analysis, chemistry, biochemistry, HPLC, LC/MS, GC, GC/MS, Melrose, Glasgow, Edinburgh, Newcastle, Berwick-upon-Tweed, Kelso, Morpeth VRS7583KF Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website
Feb 22, 2022
Full time
Fantastic opportunity for an experienced Business Development Manager seeking a new challenge! Our company is well established within the food technology industry and are able to offer a wide a range of testing services such as raw materials, nutrition, safety, packaging, QA/QC, toxins and many other services. Due to demand, they now require a Business Development Manager to secure new business in Scotland to the North East of England. This is proactive business development position where you will search and identify new opportunities through a variety of methods such as networking events, LinkedIn, responding to incoming enquires and previous leads, etc. To be considered for this role you must have: Good knowledge or experience of food or beverage manufacture/testing (gained from sales or lab experience) A proven record in Business Development Degree in a relevant subject - Chemistry/Nutrition/Biochemistry etc Knowledge and experience working with CRM systems Team player mindset, excellent interpersonal skills Above all an energetic and a desire succeed attitude! The position comes with a company car, phone, laptop etc + 10% bonus and training related to services on offer. Apply to VRS now to be considered for this exciting new opportunity! Keywords: food testing, water testing, food & beverage, Sales, service sales, food and nutritional services, food safety analysis, business development, commercial manager, acquisitions, new business, strategic, scientific sales, Analyst, chromatography, wet chemistry, analytical, analysis, chemistry, biochemistry, HPLC, LC/MS, GC, GC/MS, Melrose, Glasgow, Edinburgh, Newcastle, Berwick-upon-Tweed, Kelso, Morpeth VRS7583KF Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website
Pharmaceutical Manufacturer based in Hertfordshire seeks experienced QC Analyst's. About the role: To sample and inspect all in-coming packaging components against agreed sampling procedures and specifications. To raise a "Non-conformance" report if any material is outside of specification. Perform release and stability testing of QC samples, raw materials and packaging through HPLC, UV, Dissolution and Karl Fischer, analysis as well as physical testing of tablets, capsules and packaging. To test bulk all physical parameters for all finished product samples against the specification. To liaise with the Laboratory Supervisor/QA Manager on all aspects of results obtained which show deviance from the specification. Skills and experience: Relevant degree in a scientific discipline Previous experience working in a laboratory environment Experience of HPLC analysis and troubleshooting, ideally using Agilent systems and Open Lab software An understanding of GMP/ Pharmacopeia Experience of working in the Pharmaceutical Industry Worked by Standard Operating Procedures Proficient in the use of Microsoft Office including Word and Excel
Jan 04, 2022
Full time
Pharmaceutical Manufacturer based in Hertfordshire seeks experienced QC Analyst's. About the role: To sample and inspect all in-coming packaging components against agreed sampling procedures and specifications. To raise a "Non-conformance" report if any material is outside of specification. Perform release and stability testing of QC samples, raw materials and packaging through HPLC, UV, Dissolution and Karl Fischer, analysis as well as physical testing of tablets, capsules and packaging. To test bulk all physical parameters for all finished product samples against the specification. To liaise with the Laboratory Supervisor/QA Manager on all aspects of results obtained which show deviance from the specification. Skills and experience: Relevant degree in a scientific discipline Previous experience working in a laboratory environment Experience of HPLC analysis and troubleshooting, ideally using Agilent systems and Open Lab software An understanding of GMP/ Pharmacopeia Experience of working in the Pharmaceutical Industry Worked by Standard Operating Procedures Proficient in the use of Microsoft Office including Word and Excel
Production Support Chemist (Pharmaceuticals) Excellent Salary (Progression + 9% pension + Bonus + Benefits) Newcastle-upon-Tyne, North East (Commutable from: Blyth, Cramlington, Prudhoe, Washington, Durham) Are you a Production Chemist, with experience or knowledge in scale up or plant support, looking to join a leading pharmaceutical company where you will work on ground-breaking new products and have chance to progress technically? On offer is an excellent role, with a well-established company, where you will be recognised as a specialist in your field and be well rewarded with their generous benefits package. This company are a leading pharmaceutical manufacturer for the UK and global sphere, providing top tier customers with a crucial and innovative product that have a real and profound impact on day-to-day life. You will be fully involved with some of the newest ground breaking products within the industry. The ideal candidate will have expertise in product scale up or plant support. This is a fantastic role for a production support chemist to join a multinational organisation, offering technical progression and a varied role with excellent benefits. The Role: - Production Support Chemist for Pharmaceutical plant - Conduct research and offer operational support to improve plant processes. - Work closely with R&D and new product development teams - 12 hr shifts (4 on - 6 off, Days and Nights) The Person: - BSc or MSc in Chemistry or Chemical Engineering - Knowledge / experience in scale up or plant support - Pharmaceutical / Manufacturing experience Reference Number: 140501 Key Words: Shift analyst, qc analyst, chemist, quality control, support chemist, analytical chemist, lab team leader, process chemist, production support chemist.
Dec 08, 2021
Full time
Production Support Chemist (Pharmaceuticals) Excellent Salary (Progression + 9% pension + Bonus + Benefits) Newcastle-upon-Tyne, North East (Commutable from: Blyth, Cramlington, Prudhoe, Washington, Durham) Are you a Production Chemist, with experience or knowledge in scale up or plant support, looking to join a leading pharmaceutical company where you will work on ground-breaking new products and have chance to progress technically? On offer is an excellent role, with a well-established company, where you will be recognised as a specialist in your field and be well rewarded with their generous benefits package. This company are a leading pharmaceutical manufacturer for the UK and global sphere, providing top tier customers with a crucial and innovative product that have a real and profound impact on day-to-day life. You will be fully involved with some of the newest ground breaking products within the industry. The ideal candidate will have expertise in product scale up or plant support. This is a fantastic role for a production support chemist to join a multinational organisation, offering technical progression and a varied role with excellent benefits. The Role: - Production Support Chemist for Pharmaceutical plant - Conduct research and offer operational support to improve plant processes. - Work closely with R&D and new product development teams - 12 hr shifts (4 on - 6 off, Days and Nights) The Person: - BSc or MSc in Chemistry or Chemical Engineering - Knowledge / experience in scale up or plant support - Pharmaceutical / Manufacturing experience Reference Number: 140501 Key Words: Shift analyst, qc analyst, chemist, quality control, support chemist, analytical chemist, lab team leader, process chemist, production support chemist.
Role Overview We are currently looking for a Senior QC Materials Analyst to join a growing biotechnology company based in South West London. As the Senior QC Materials Analyst you will work in the quality control department and you will be responsible for working with raw materials and establishing raw materials policy, flow strategy and processes. Duties and Responsibilities You will lead the sampling and testing of raw materials. You will work with programme management, quality, supply chain, development and manufacturing to meet deliverables and deadlines. As the Senior QC Materials Analyst you will be responsible for writing appropriate documentation such as materials policies, ensuring compliance and safety before releasing them. You will define management and flow strategies of product intermediates, raw materials, standards and consumables. You will support out of specification investigations, deviations, change controls related to raw materials. As the Senior QC Materials Analyst maintaining calibration, qualification and validation of material testing equipment will be among your duties. Education and Experience MSc or BSc in a relevant Scientific discipline and a number of years of industry experience working in QC including extensive experience with raw materials. Proven industry experience working in a GMP laboratory in a pharmaceutical or biotechnology/biopharma company is essential to your application. Proven experience with reagent preparation and material handling is essential for this position. To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales
Dec 02, 2021
Full time
Role Overview We are currently looking for a Senior QC Materials Analyst to join a growing biotechnology company based in South West London. As the Senior QC Materials Analyst you will work in the quality control department and you will be responsible for working with raw materials and establishing raw materials policy, flow strategy and processes. Duties and Responsibilities You will lead the sampling and testing of raw materials. You will work with programme management, quality, supply chain, development and manufacturing to meet deliverables and deadlines. As the Senior QC Materials Analyst you will be responsible for writing appropriate documentation such as materials policies, ensuring compliance and safety before releasing them. You will define management and flow strategies of product intermediates, raw materials, standards and consumables. You will support out of specification investigations, deviations, change controls related to raw materials. As the Senior QC Materials Analyst maintaining calibration, qualification and validation of material testing equipment will be among your duties. Education and Experience MSc or BSc in a relevant Scientific discipline and a number of years of industry experience working in QC including extensive experience with raw materials. Proven industry experience working in a GMP laboratory in a pharmaceutical or biotechnology/biopharma company is essential to your application. Proven experience with reagent preparation and material handling is essential for this position. To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales
QC Analyst Location: Dartford Entrust Resource Solutions are currently supporting our Pharmaceutical client in Dartford in their search for a QC Analyst. The successful candidate will perform analysis on analytical samples in accordance with defined analytical methods and Standard Operating Procedures. This will be done in line with GMP and within agreed timelines. What do we need from you? To understand basic principles of PSA / HPLC/DSC equipment and methods To swab processing equipment Prepare test methods for analytical testing and cleaning verification analysis. Prepare Standard Operating Procedures (SOP's), including corporate and departmental guidelines. Prepare analytical test reports for submissions to clients or the Company's other departments. These include, but are not limited to, Statement of Results, Certificate of Analysis and Cleaning Certificates, Method Qualification/Validation Protocols, Method Qualification/Validation Reports and Laboratory Technical Transfer Studies. Experience of GMP requirement with regards to Deviation management, out of specification investigation, reporting incidents, out of tolerance and change controls. Ensure that instrumentation used is correctly calibrated and operated in accordance with SOPs or client/manufacturing instructions. Ensure compliance with data integrity requirements of laboratory equipment and software systems. Communicate with the QC Laboratory staff, QC Manager, Operations, QA, client representatives To apply, please send an up to date copy of your CV to Lynsey today
Nov 08, 2021
Contractor
QC Analyst Location: Dartford Entrust Resource Solutions are currently supporting our Pharmaceutical client in Dartford in their search for a QC Analyst. The successful candidate will perform analysis on analytical samples in accordance with defined analytical methods and Standard Operating Procedures. This will be done in line with GMP and within agreed timelines. What do we need from you? To understand basic principles of PSA / HPLC/DSC equipment and methods To swab processing equipment Prepare test methods for analytical testing and cleaning verification analysis. Prepare Standard Operating Procedures (SOP's), including corporate and departmental guidelines. Prepare analytical test reports for submissions to clients or the Company's other departments. These include, but are not limited to, Statement of Results, Certificate of Analysis and Cleaning Certificates, Method Qualification/Validation Protocols, Method Qualification/Validation Reports and Laboratory Technical Transfer Studies. Experience of GMP requirement with regards to Deviation management, out of specification investigation, reporting incidents, out of tolerance and change controls. Ensure that instrumentation used is correctly calibrated and operated in accordance with SOPs or client/manufacturing instructions. Ensure compliance with data integrity requirements of laboratory equipment and software systems. Communicate with the QC Laboratory staff, QC Manager, Operations, QA, client representatives To apply, please send an up to date copy of your CV to Lynsey today
CK Group are recruiting for a QC Analyst to join a long established manufacturer of OTC medicinal products and independent UK pharmaceutical company at their site in Hertfordshire on a permanent basis. The Company: Having been established almost 60 years ago, this company focuses on researching and development novel treatments. Location: This role is located in Hertfordshire. It is easily commutable from the surrounding areas with excellent road links to the M25, M11 and A10. Salary: Competitive. QC Analyst Role: Your responsibilities will be to: -Perform routine and non-routine testing activities of raw materials, bulk and finished packaged samples. -Primarily use analytical techniques such as HPLC, GC and wet chemical techniques. -Perform the testing of samples in compliance with authorised test procedures. Your Background: As a QC Analyst you will require: -A relevant BSc (or above) in chemistry or a related field. -Relevant industry experience in an analytical testing role, preferably in a GMP environment. -Experience of GC and HPLC analysis. Apply: Entitlement to work in the UK is essential. Please quote referenvce 51439
Sep 13, 2021
Full time
CK Group are recruiting for a QC Analyst to join a long established manufacturer of OTC medicinal products and independent UK pharmaceutical company at their site in Hertfordshire on a permanent basis. The Company: Having been established almost 60 years ago, this company focuses on researching and development novel treatments. Location: This role is located in Hertfordshire. It is easily commutable from the surrounding areas with excellent road links to the M25, M11 and A10. Salary: Competitive. QC Analyst Role: Your responsibilities will be to: -Perform routine and non-routine testing activities of raw materials, bulk and finished packaged samples. -Primarily use analytical techniques such as HPLC, GC and wet chemical techniques. -Perform the testing of samples in compliance with authorised test procedures. Your Background: As a QC Analyst you will require: -A relevant BSc (or above) in chemistry or a related field. -Relevant industry experience in an analytical testing role, preferably in a GMP environment. -Experience of GC and HPLC analysis. Apply: Entitlement to work in the UK is essential. Please quote referenvce 51439
SENIOR QC ANALYSTS - Ruislip Salary circa - £24 - £30k plus benefits SyriMed Limited, part of B&S Group, are looking for a number of Senior QC Analysts to join a growing team based in our modern QC Laboratory at our prestigious Ruislip Site You will be working within a team of Pharmaceutical QC Analysts on the routine testing of mainly finished products (majority liquids), but there may be some r...... click apply for full job details
Mar 17, 2021
Full time
SENIOR QC ANALYSTS - Ruislip Salary circa - £24 - £30k plus benefits SyriMed Limited, part of B&S Group, are looking for a number of Senior QC Analysts to join a growing team based in our modern QC Laboratory at our prestigious Ruislip Site You will be working within a team of Pharmaceutical QC Analysts on the routine testing of mainly finished products (majority liquids), but there may be some r...... click apply for full job details