Responsibilities : Development/Improvement activities: Serve as SME to support Site/Global projects. Proactively identifies scope for improvement or development based on knowledge of short to mid-term business needs. Leads and develops a strategy, plans and manages projects for method development or improvement as identified. Makes data supported decisions on project progression; uses technical expertise to overcome analytical issues. Documents project work as detailed lab book records or under technical protocols and reports as appropriate. Disseminates project findings/status updates at regular meetings/forums within Global AS&T. Represents as an interface between AS&T and key stakeholders (QC, MS&T, Regulatory Affairs). Operations Support: Participates in lab work-load planning with the wider team. Design work plans/projects with a compliance development mindset i.e., GMP adherence. Performs tests in accordance with established methods and properly documents test results. Provides guidance/mentorship/training to other lab staff as required. Evaluates performance of analytical instruments and equipment and recommends new acquisition or replacements initiatives. Authors/Reviewer protocols and reports for suitability studies and investigations to support testing and compliance issues, technical writing proficient. Ensures laboratory instruments are qualified, calibrated and properly maintained and documentation complies with cGMP standards. Assists and maintains standard operating procedures (SOPs), risk assessments and other quality documentation as required. Documents quality issues and performance measures for management review. Qualifications : Bachelor's degree in a relevant scientific discipline (Chemistry, Biochemistry.) MSc (d esirable ) PhD (d esirable ) A recognized expert in Analytical and Biological methods (CE, ELISA, SDS-PAGE) Experience of working in pharmaceuticals, particularly biologics is advantageous. Experience of assay development and validation essential. Assay lifecycle from proof of concept to registration and change management. Desirable to have experience of process or product characterization using a variety orthogonal method. Desirable to have people leader experience and or leading project teams. Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable. Our Benefits CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus. About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about CSL Seqirus . We want Seqirus to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL Seqirus. Do work that matters at CSL Seqirus! Watch our 'On the Front Line' video to learn more about CSL Seqirus
Mar 25, 2024
Full time
Responsibilities : Development/Improvement activities: Serve as SME to support Site/Global projects. Proactively identifies scope for improvement or development based on knowledge of short to mid-term business needs. Leads and develops a strategy, plans and manages projects for method development or improvement as identified. Makes data supported decisions on project progression; uses technical expertise to overcome analytical issues. Documents project work as detailed lab book records or under technical protocols and reports as appropriate. Disseminates project findings/status updates at regular meetings/forums within Global AS&T. Represents as an interface between AS&T and key stakeholders (QC, MS&T, Regulatory Affairs). Operations Support: Participates in lab work-load planning with the wider team. Design work plans/projects with a compliance development mindset i.e., GMP adherence. Performs tests in accordance with established methods and properly documents test results. Provides guidance/mentorship/training to other lab staff as required. Evaluates performance of analytical instruments and equipment and recommends new acquisition or replacements initiatives. Authors/Reviewer protocols and reports for suitability studies and investigations to support testing and compliance issues, technical writing proficient. Ensures laboratory instruments are qualified, calibrated and properly maintained and documentation complies with cGMP standards. Assists and maintains standard operating procedures (SOPs), risk assessments and other quality documentation as required. Documents quality issues and performance measures for management review. Qualifications : Bachelor's degree in a relevant scientific discipline (Chemistry, Biochemistry.) MSc (d esirable ) PhD (d esirable ) A recognized expert in Analytical and Biological methods (CE, ELISA, SDS-PAGE) Experience of working in pharmaceuticals, particularly biologics is advantageous. Experience of assay development and validation essential. Assay lifecycle from proof of concept to registration and change management. Desirable to have experience of process or product characterization using a variety orthogonal method. Desirable to have people leader experience and or leading project teams. Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable. Our Benefits CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus. About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about CSL Seqirus . We want Seqirus to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL Seqirus. Do work that matters at CSL Seqirus! Watch our 'On the Front Line' video to learn more about CSL Seqirus
This Compliance Officer role is available within a globally renowned Chemical manufacturing company, committed to investing significantly in the successful candidate's career and personal growth. The position offers a salary of up to 30,000 per annum, along with a profit share bonus tied to performance after nine months of employment. As a Compliance Officer, you'll be responsible for providing technical and administrative support to ensure product compliance with global chemical legislation. This includes managing chemical-specific data and documentation for both raw materials and finished goods, fostering effective communication with various departments, and collaborating closely with the Regulatory Manager to develop and enforce departmental procedures in line with the company's policies. Compliance Officer Responsibilities Ensure adherence to the company's safety culture and maintain health, safety, and environmental standards consistently. Manage crucial raw material data and facilitate the introduction of new materials through the company's change management process. Assist the regulatory manager in maintaining data for raw materials and finished products in the company's SDS authoring software. Author and release Safety Data Sheets and label content according to established procedures. Offer insights for customer inquiries and distribute documents to customers. Aid the regulatory compliance manager in compiling and presenting departmental KPIs. Generate monthly reports to monitor import volumes, sales, and inventory levels to support COMAH and REACH. Assist the Manager in implementing the global strategy, including supporting REACH registrations, global notifications, reviewing global inventories, and handling poison centre notifications. Please apply directly for further information regarding this Compliance officer role.
Mar 22, 2024
Full time
This Compliance Officer role is available within a globally renowned Chemical manufacturing company, committed to investing significantly in the successful candidate's career and personal growth. The position offers a salary of up to 30,000 per annum, along with a profit share bonus tied to performance after nine months of employment. As a Compliance Officer, you'll be responsible for providing technical and administrative support to ensure product compliance with global chemical legislation. This includes managing chemical-specific data and documentation for both raw materials and finished goods, fostering effective communication with various departments, and collaborating closely with the Regulatory Manager to develop and enforce departmental procedures in line with the company's policies. Compliance Officer Responsibilities Ensure adherence to the company's safety culture and maintain health, safety, and environmental standards consistently. Manage crucial raw material data and facilitate the introduction of new materials through the company's change management process. Assist the regulatory manager in maintaining data for raw materials and finished products in the company's SDS authoring software. Author and release Safety Data Sheets and label content according to established procedures. Offer insights for customer inquiries and distribute documents to customers. Aid the regulatory compliance manager in compiling and presenting departmental KPIs. Generate monthly reports to monitor import volumes, sales, and inventory levels to support COMAH and REACH. Assist the Manager in implementing the global strategy, including supporting REACH registrations, global notifications, reviewing global inventories, and handling poison centre notifications. Please apply directly for further information regarding this Compliance officer role.
CY Partners have an exciting new opportunity with a global industry leader in fuels and lubricants. Product Stewardship & Regulatory Compliance (PSRC) is about understanding, controlling and communicating a product's environmental, health and safety related effects throughout its lifecycle from development, through to manufacture and final disposal. The role of Product Stewardship Advisor will appeal to candidates from the chemical industry experienced in understanding chemical regulations and translating them into compliance systems and assessing their implications on operations and product supply. Key Responsibilities Accountability for maintaining chemical regulatory compliance in the EMEA countries as allocated Responsibility for completing regulatory notification & reporting requirements in designated countries (Eg. EU PIC, WGK nominations, EU REACH, GB REACH, EAEU REACH, etc.) Provide technical expertise to regulatory assessments of new product developments, including country-specific substance notifications Supporting other colleagues in the global team to meet local regulatory compliance requirements Track, evaluate and conduct impact analyses of regulatory or substance-lead changes, with development of compliance strategies and coordination of timely implementation of action plans Engagement with internal stakeholders to determine effective resolution on regulatory issues Provide regulatory guidance to regional manufacturing plants, Sales & Marketing functions, and support external customer enquiries Support and develop process improvements, SOPs and implementation of best practices to ensure regulatory compliance Key Requirements: Bachelor s degree (or equivalent) in chemistry or a related scientific discipline (or equivalent experience). Strong organic chemistry background is beneficial. Strong understanding of the fundamental principles behind GHS for classification of hazardous chemicals. Knowledge and experience of chemical substance regulations, regulatory reporting requirements, substance inventory notification schemes, and transport regulations across the EMEA region. Excellent problem-solving skills and understanding of the interconnectivity of regulatory data. Some familiarity with SAP EHS linked to SDS authorship or Substance Volume Tracking would be an advantage. Good interpersonal and communication skills Please apply directly, if you have any questions about the role contact Joe at CY Partners.
Mar 22, 2024
Full time
CY Partners have an exciting new opportunity with a global industry leader in fuels and lubricants. Product Stewardship & Regulatory Compliance (PSRC) is about understanding, controlling and communicating a product's environmental, health and safety related effects throughout its lifecycle from development, through to manufacture and final disposal. The role of Product Stewardship Advisor will appeal to candidates from the chemical industry experienced in understanding chemical regulations and translating them into compliance systems and assessing their implications on operations and product supply. Key Responsibilities Accountability for maintaining chemical regulatory compliance in the EMEA countries as allocated Responsibility for completing regulatory notification & reporting requirements in designated countries (Eg. EU PIC, WGK nominations, EU REACH, GB REACH, EAEU REACH, etc.) Provide technical expertise to regulatory assessments of new product developments, including country-specific substance notifications Supporting other colleagues in the global team to meet local regulatory compliance requirements Track, evaluate and conduct impact analyses of regulatory or substance-lead changes, with development of compliance strategies and coordination of timely implementation of action plans Engagement with internal stakeholders to determine effective resolution on regulatory issues Provide regulatory guidance to regional manufacturing plants, Sales & Marketing functions, and support external customer enquiries Support and develop process improvements, SOPs and implementation of best practices to ensure regulatory compliance Key Requirements: Bachelor s degree (or equivalent) in chemistry or a related scientific discipline (or equivalent experience). Strong organic chemistry background is beneficial. Strong understanding of the fundamental principles behind GHS for classification of hazardous chemicals. Knowledge and experience of chemical substance regulations, regulatory reporting requirements, substance inventory notification schemes, and transport regulations across the EMEA region. Excellent problem-solving skills and understanding of the interconnectivity of regulatory data. Some familiarity with SAP EHS linked to SDS authorship or Substance Volume Tracking would be an advantage. Good interpersonal and communication skills Please apply directly, if you have any questions about the role contact Joe at CY Partners.
This is a very exciting opportunity to join a successful chemicals consultancy and benefit from full training in chemical regulatory affairs activities such as SDS authoring, hazard classifications, labelling and poison centre notifications. You will work with and be trained by a well-known and industry leading expert. There is also huge potential for career development with scope for you to move into regulatory expert and management positions in realistic timeframes. You are likely to be a chemist with an interest in chemical legislation/regulation, be willing to conduct a broad range of tasks, and be able to learn quickly. You will have excellent communication skills, a flexible and adaptable approach and ideally have some regulatory knowledge eg CLP or REACH. Initially you will assist the Senior Consultant and shadow the Director learning how the business operates. A rare and very exciting opportunity. Key Skills: Regulatory Affairs, hazard communication, hazard classification, CLP, GHS, PCNs, customer service, consulting, quick learning, adaptable, good communication, ambitious. VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.
Mar 21, 2024
Full time
This is a very exciting opportunity to join a successful chemicals consultancy and benefit from full training in chemical regulatory affairs activities such as SDS authoring, hazard classifications, labelling and poison centre notifications. You will work with and be trained by a well-known and industry leading expert. There is also huge potential for career development with scope for you to move into regulatory expert and management positions in realistic timeframes. You are likely to be a chemist with an interest in chemical legislation/regulation, be willing to conduct a broad range of tasks, and be able to learn quickly. You will have excellent communication skills, a flexible and adaptable approach and ideally have some regulatory knowledge eg CLP or REACH. Initially you will assist the Senior Consultant and shadow the Director learning how the business operates. A rare and very exciting opportunity. Key Skills: Regulatory Affairs, hazard communication, hazard classification, CLP, GHS, PCNs, customer service, consulting, quick learning, adaptable, good communication, ambitious. VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.
A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. Your role:we currently have an exciting opportunity for a talented Associate Scientist to join our Analytical Chemistry Department in Glasgow. In this role, you will perform a wide variety of routine and custom assays to GMP standards. The main analytical techniques you will use are HPLC, UHPLC, iCE,SDS-Page, IEF, CE, UV and particle counting. You will also have responsibilities for laboratory housekeeping, preparation of reagents, stock control and equipment maintenance. Who you are: You will have a university degree in chemistry, biochemistry or a closely related subject. You will ideally have laboratory experience in an industrial setting, within a GMP environment. You will have a good knowledge of a wide range of modern analytical techniques You will be hard-working, self-motivated and enjoy working in a team environment You will possess excellent oral and written communication skills, as well as good IT skills What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life! Curious? Apply and find more information at We are committed to promoting a diverse and inclusive workforce. Applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships. Job Requisition ID: 239630 Location: Glasgow Career Level: B - Recent University Graduate( Working time model: Careers during Covid-19 Thank you for visiting our careers website, we are always looking for curious minds to join our teams. We understand how much the world is being impacted by the Covid-19 crisis and we want to assure you that your safety is very important to us. To ensure that everyone's health is protected, instead of a standard face-to-face interview, it is likely that you will be offered alternative digital interview options. US employees must be fully vaccinated against COVID-19 prior to your start date unless an accommodation is granted by the Company. The Company uses the definition of "fully vaccinated" assigned by the Centers for Disease Control & Prevention for purposes of considering satisfaction of this requirement which is a condition of employment. Notice on Fraudulent Job Offers Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information .
Feb 21, 2022
Full time
A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. Your role:we currently have an exciting opportunity for a talented Associate Scientist to join our Analytical Chemistry Department in Glasgow. In this role, you will perform a wide variety of routine and custom assays to GMP standards. The main analytical techniques you will use are HPLC, UHPLC, iCE,SDS-Page, IEF, CE, UV and particle counting. You will also have responsibilities for laboratory housekeeping, preparation of reagents, stock control and equipment maintenance. Who you are: You will have a university degree in chemistry, biochemistry or a closely related subject. You will ideally have laboratory experience in an industrial setting, within a GMP environment. You will have a good knowledge of a wide range of modern analytical techniques You will be hard-working, self-motivated and enjoy working in a team environment You will possess excellent oral and written communication skills, as well as good IT skills What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life! Curious? Apply and find more information at We are committed to promoting a diverse and inclusive workforce. Applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships. Job Requisition ID: 239630 Location: Glasgow Career Level: B - Recent University Graduate( Working time model: Careers during Covid-19 Thank you for visiting our careers website, we are always looking for curious minds to join our teams. We understand how much the world is being impacted by the Covid-19 crisis and we want to assure you that your safety is very important to us. To ensure that everyone's health is protected, instead of a standard face-to-face interview, it is likely that you will be offered alternative digital interview options. US employees must be fully vaccinated against COVID-19 prior to your start date unless an accommodation is granted by the Company. The Company uses the definition of "fully vaccinated" assigned by the Centers for Disease Control & Prevention for purposes of considering satisfaction of this requirement which is a condition of employment. Notice on Fraudulent Job Offers Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information .