2093 Biotech jobs

Design Manager - Construction Location: West Midlands - Birmingham Salary: Up to £65,000 + Car or Allowance, Pension, Health Company: Expanding Main Contractor The Opportunity Are you a Design Manager looking for a genuine opportunity to progress your career to the next level..... click apply for full job details

Design Coordinator - Construction Location: Birmingham Salary: £30k - £40k + Car allowance, Pension, Health Company: Expanding Main Contractor The Opportunity Are you a Design Coordinator looking for a genuine opportunity to progress your career to the next level? If so..... click apply for full job details

International Market Research & Insights Lead (Medical Aesthetics & Consumer) Our client is a unique, global healthcare company who is focused on developing, manufacturing and commercialising innovative branded pharmaceuticals, high-quality generic and over-the-counter medicines and biologic products for patients around the..... click apply for full job details

Graduate Design Engineer - Electronics/Firmware If you are a recent graduate from an Electronics Engineering degree and seeking swift career progression with a global company then please apply to this Design Engineer role. The successful Engineer will be working within a growing Design Engineering team and focusing on a..... click apply for full job details

Senior Acoustic Consultant - Required for our client, a leading independent consultancy based in their Woking office. Our client are specialists within Civil Engineering, Highway, Transportation and Infrastructure and are seeking a Senior Acoustic Consultant for their Environment team. This opportunity requires an..... click apply for full job details

Senior Product Designer Bristol £40000 - £50000 + Benefits THE ROLE You will be responsible for the design and specification of our product, particularly in the earlier stages where thorough medical understanding is fundamental Good drawing and model-making skills are also..... click apply for full job details

Graduate Design Engineer (Electronics/Firmware) Maidenhead Up to £30,000 My client is a well-established, rapidly growing international manufacturing business with innovative ideas and a distinct & successful product range looking for a Graduate Design Engineer to join the team. The opportunities for career development..... click apply for full job details

Formulation Chemist - Personal Care Deeside Circa £35,000 + Benefits Experienced formulation chemist wanted to join a leading manufacturer of branded personal care products, located in North Wales. I am looking for an exceptional chemist with a broad range of product experience within the cosmetics..... click apply for full job details

An important shift-based Process Quality Chemist role is vacant at a large speciality chemicals company based in the Humberside region. This Process Quality Chemist role will not have any management duties but will involve a highly personable and reliable professional outlook and a basic chemical testing skillset...... click apply for full job details

Our client, a successful and growing financial services organisation, are seeking a Will Drafter to join their Estate Planning department Reporting to the Operations & Product Technical Manager, the successful Will Drafter will deliver a post sales service, developing customer Instructions for Wills..... click apply for full job details

Contract Requirement Data Scientist - Machine Learning A Data Scientist with experience of Machine Learning, Python and Cloud technologies is required for a London based client. You will be expected to define data pipelines, produce production models which connect to apps, and work with initial data to..... click apply for full job details

JOB SUMMARY Opportunity for an experienced MSL to join this International Lifecycle Pharma Company, to focus on a new product's launch, within Anti-Infectives. This role is field based managing the South Eastern territory. BACKGROUND International Pharmaceutical Company - specializing in..... click apply for full job details

6 Month Fixed Term Contract (FTC) + Extension Are you a 3D Visualiser / Graphic Artist, with experience of CGI / Modelling, looking for an immediately available, 6 month fixed term contract role with flexible working hours for one of the UK's leading media production companies? On offer is varied role offering full..... click apply for full job details

JOB SUMMARY Opportunity for an experienced MSL to join this International Lifecycle Pharma Company, to focus on a new product's launch, within Anti-Infectives. This role is field based managing the Northern territory. BACKGROUND International Pharmaceutical Company - specializing in..... click apply for full job details

We have an exciting opportunity for a Data Analyst to deliver a high quality service to our client working Monday - Friday 8.30am - 5pm working as part of a team in an open plan office, ensuring that tasks are carried out efficiently and to the highest standard possible. Working as part of a close knit team..... click apply for full job details

Are you a contract draughtsperson? Are you looking for a new, long term contract? Have you used Tekla? A Tekla draughtsperson is required for a long term contract in North London. My client have been fabricating specialist metalwork for over 30 years, they create the initial drawings and then carry out the cutting and welding..... click apply for full job details

Design Manager - Permanent - Residential Main Contractor Competitive salary + package (negotiable) Bristol This is an opportunity for an experienced construction Design Manager to work for a leading Residential main contractor who pride themselves in delivering quality Housing developments..... click apply for full job details

JOB SUMMARY Opportunity for an experienced MSL to join this International Lifecycle Pharma Company, to focus on a new product's launch, within Anti-Infectives. This role is field based managing the South Western territory. BACKGROUND International Pharmaceutical Company - specializing in..... click apply for full job details

Role: Mid-Weight Graphic Designer Location: Central Bristol Salary: Competitive + Benefits Are you a mid-weight graphic designer who's worked in-house or in a studio environment with proven experience working with big-name brands? Do you have proven experience with print and digital design..... click apply for full job details

Job Title: CAD Technician Location: Keighley Hours of work: 39 Salary: £18500 Benefits: company bonus scheme up to £120 a month, 2 x life assurance, 22 days plus stat holiday (soon to be increased to 25), pension matched up to 5%. Main Function..... click apply for full job details

Design Technician North Yorkshire £££ Salary up to £30,000 Working as part a factory-based product design team, under the leadership of the Design Team Leader, the Design Technicians play a pivotal role in driving and controlling the Engineering Change Request system as the design evolves...... click apply for full job details

Instructional Designer/ Material Developer - East Berkshire An outstanding opportunity at the multinational consumer healthcare organisation. We are seeking an experienced Technical Trainer with material development experience to support the successful implementation of the global programme by being responsible for the..... click apply for full job details

Job Title: Solution Designer (REST API, J2EE, node.js) Location: Central London Salary: £80 - £85,000K per annum plus Bonus, Benefits and Pension Start: ASAP We have an exciting opportunity for a Solution Designer (REST API, J2EE, node.js) to join an established team within a global($15bn)..... click apply for full job details

We are currently looking for a Principle Scientist to join a leading Biotechnology company based in the Berkshire area. As the Principle Scientist you will be responsible for product and process development to support the manufacturing of antibodies and recombinant proteins. KEY DUTIES AND RESPONSIBILITIES:..... click apply for full job details

The Job: Instrument and experimental design. Planning and execution of experiments. Analysis of data. Modelling. Formulation and presentation of conclusions and Report writing. The Duties: Responsible for aspects of research, development, implementation, design and analysis of technical prototype..... click apply for full job details

An outstanding opportunity to work with a much sought after CRO. They are looking for CRA with around 18-24 months' experience. They provide unparalleled opportunities for career growth and development. As a CRA working within the clinical operations team you will be at the forefront of clinical trials practice..... click apply for full job details

We currently require a Mechanical Draughtsman who is highly competent and experienced in Autodesk Inventor 3D software. The role will be responsible for the 3D design of structural components and machinery design across a number of industries. You will be using Inventor CAD software and responsible for the CAD design of..... click apply for full job details

CAD Technician (AutoCAD 3D) £22,000- £26,000 + Training + 31 Days Holiday + Pension + Company Benefits Birmingham, West Midlands - commutable from Coventry, Wolverhampton, Redditch Are you a CAD Technician with experience using AutoCAD 3D who is looking for specialist design training where you will be working for an..... click apply for full job details

Brand new CRA / SCRA roles as part of a new project team. I am currently recruiting for CRAs to be based throughout the UK on behalf of a Global player within the Pharmaceutical industry. You will be primarily tasked to set up and monitor clinical trials conducted in the United Kingdom as part of international..... click apply for full job details

Are you an experienced synthetic organic chemist coming to the end of your PhD or postdoctoral contract? Are you looking to apply your synthetic chemistry knowledge in industry? If so, then this is the perfect opportunity for you! Our client is a contract research organisation working at the cutting edge of..... click apply for full job details

AutoCAD MEP Draughtsperson (Plant Layouts etc.) Wiltshire 6 Month Contract + Likely 6 Month extension £30.00 - £37.00hr (Umbrella / Ltd Co) Are you an experienced AutoCAD MEP Draughtsperson with prior experience in Plant Layouts? Are you looking for your next immediately available, days based contract role whilst..... click apply for full job details

Fantastic opportunity for a chemist or biochemist keen to develop their career in biochemistry within a fast-growing biopharmaceutical laboratory. You will be working as part of a highly regarded and successful team utilising an extensive range of analytical instrumentation to provide bespoke analytical science services. ..... click apply for full job details

Exciting opportunity for an enthusiastic chemist or biochemist keen to join a rapidly growing biopharmaceutical laboratory. You will be working as part of a highly regarded and successful team providing an extensive range of protein biochemistry services in support of biopharmaceutical development..... click apply for full job details

We have a great opportunity for a full time Senior Laser Therapist at a busy Aesthetics Clinic in Central Birmingham. We are recruiting for a Senior Therapist who can demonstrate a high standard of professionalism and attention to detail. Due to Company expansion we require a friendly and enthusiastic laser therapist..... click apply for full job details

We are pleased to be working with a leading global media company as they look to appoint and experienceService Design Lead. Reporting to the Senior Programme Manager, you will be part of a key team responsible for defining and implementing the target operational model which will enable successful operation and delivery of..... click apply for full job details

For our Dudley based client we are currently looking for an experienced Information Analyst to support the delivery and continual improvement of a high quality performance information service. The role involes to: provide essential performance data and analysis, contribute to continuing development..... click apply for full job details

My client is looking for a CAD Engineer based in Kent to design and develop their products from concept through to production. Client Details My client has been creating furniture for demanding spaces for over 4 decades with a focus on enhancing the environments of their customers by providing style and quality..... click apply for full job details

We're one of the most experienced providers of clinical homecare in the UK and we are currently recruiting a Quality Assurance Officer to join our QA Team based in Harlow. The QA Department supports our busy aseptic manufacturing facility, which operates 24 hours a day Monday to Friday. The purpose of the role is to Quality Assure the Final Release aseptically manufactured products and participate in various aspects of the QA department. Your key accountabilities will include; The checking of batch manufacturer records against orders/ prescriptions and stability data ensuring Good Manufacturing Practice is followed throughout the production process Physical checks of products Problem solving and investigation into issues Reviewing non-conformances and determining the risk to product and categorisation of the incident Determining appropriate CAPA responses to incidents We are looking for someone with previous experience working in a GMP environment along with a Quality Assurance/ or Control department industry exposure. You will also have excellent attention to detail, be a great communicator and be confident using Microsoft Word and Excel. As well as working for an organisation that has the patient at the heart of everything we do, we will reward you with a Competitive basic salary, Company Pension scheme,28 days annual leave (includes statutory holidays), heavily discounted healthcare insurance and a childcare voucher scheme. We provide care to more than 70,000 patients ranging from straightforward delivery of medication, to specialist nursing for complex conditions. We work in partnership with the NHS, pharmaceutical companies, private medical insurers and consultants. We're passionate about what we do and the difference we make to our patients' lives. It's this dedication that ensures we constantly deliver outstanding levels of care to our patients. We used to be called Bupa Home Healthcare and in July 2016 we were acquired by the Celesio UK group of companies, a leading provider of healthcare services, including LloydsPharmacy.

Clinical PM (Clinical Project Manager) office based 50,000 - 60,000 depending on experience *Large leading global Bio-pharmaceutical organisation, based on the Scottish border currently require an office based Clinical PM (Clinical Project Manager) One of the leading Bio-pharmaceutical organisations, based on the Scottish border, currently require a Clinical PM (Clinical Project Manager) to join their clinical team working on several global Clinical Studies in various therapeutic areas across the UK. This is the perfect opportunity for both a highly experienced Junior Project Manager and Project Manager with global experience to join a Leading Bio-pharmaceutical firm to fully run multiple studies in various therapy areas from start to finish across phase 1 to post marketing. Responsibilities; Project manage across all stages of clinical development (phase 1 - post marketing) Create full project plans and schedules Create and maintain all project documents such as project charter, risk logs, communication plans, etc. Responsible for study budgets and timeline management Ensure all project sub teams adhere to the approved clinical development plan. Support all organisational activities such as resource management and process improvement Required skills; Life science related Degree 2-4 years Project Management experience Global Project Management experience Office based This is a permanent, office based position. The successful candidate will be rewarded with a competitive basic salary and package. If this role is of interest, please send your CV to or call Clinical Professionals is a leading pharmaceutical staffing business. We have been placing professional within clinical research for over 10 years so have unrivalled knowledge of the market and can give tailored advice for you and outstanding levels of service throughout your career. We also have great relationships with our clients so pride ourselves on being able to identify clients that may be the perfect fit for you and bring you to their attention. By working proactively with candidates we find you the RIGHT job at the RIGHT time.

Do you have experience in a Quality Assurance/ Quality Control role? With good understanding of a GMP laboratory? Are you a team player looking for new challenges? We are looking for an outstanding candidate for a GMP Training Manager position within a global pharmaceutical testing company. The successful candidate will fill an essential role ensuring the smooth running of the department. You will operate and manage the GMP training process and provide continuous improvement in overall GMP compliance; overseeing records, mentoring new staff and undertaking annual reviews. The ideal candidate will possess: Experience in a GMP laboratory, working with QA or QC Management experience is desirable but not essential Desire to develop and learn new skills Be a team player; working with staff of all levels Excellent communication written and verbal Apply to VRS now to be considered for this exciting opportunity! Key words: GMP, QA, QC, Good Manufacturing Practice, Quality Assurance, Quality Control, Management, Training, South East, Cambridgeshire, Hertfordshire, VRS6109HQ . 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 websit

Clinical Trial Manager Oncology (CTM) 50,000 - 60,000 depending on experience + car allowance *Leading global Pharmaceutical firm, based in Hertfordshire, currently require an office based Clinical Trial manager (CTM) with up to 2 days from home* One of the leading Pharmaceutical firms, based in Hertfordshire, currently require a Clinical Trial manager (CTM) to join their clinical team to manage 1 or more Oncology studies ensuring all study milestones and deliverables are met. This is a pivotal position, perfect for a Clinical Trial manager (CTM) with extensive Project management experience within Oncology studies in a CRO looking to move into a Pharmaceutical environment, alternatively an individual from a medium pharmaceutical looking for a bigger challenge. Responsibilities; Budget management. Involvement in process improvement activities Provide input into the development and review of high level study documents Extensive management, monitoring and reviewing of CRO/Vendors Act as first point of contact for CROs and study sites. Monitor expenses of work teams to anticipate issues with cost. Mentor team members on process and systems Possible line management Required skills; Minimum 2-years global clinical project management experience Extensive Oncology knowledge and experience through phase 1-3 Mentoring experience CRO/Vendor management experience This is a permanent, office-based position. The successful candidate will be rewarded with a competitive basic salary and package. If this role is of interest, please send your CV to or call Clinical Professionals is a leading pharmaceutical staffing business. We have been placing professional within clinical research for over 10 years so have unrivalled knowledge of the market and can give tailored advice for you and outstanding levels of service throughout your career. We also have great relationships with our clients so pride ourselves on being able to identify clients that may be the perfect fit for you and bring you to their attention. By working proactively with candidates we find you the RIGHT job at the RIGHT time.

Director of Clinical Operations (Oncology) 75,000 - 86,000 depending on experience + car allowance *Leading global Pharmaceutical firm, based in Hertfordshire, currently require a Director of Clinical Operations to be office based with up to 2 days from home* One of the leading Pharmaceutical firms, based in Hertfordshire, currently require a Director of Clinical Operations to join their clinical development team to be responsible for the provision of medical oversight and input through phases 1-3 on all Oncology studies. This is the perfect opportunity for a Director of Clinical Operations with a years experience from a CRO looking to move into a Pharmaceutical environment, alternatively an individual from a medium pharmaceutical looking for a bigger challenge. Responsibilities; Oversight of clinical project teams Create, implement and direct clinical research plans and programs adhering to the established design principles. Lead the development of Clinical Protocols, meeting CDP objectives Create and implement new strategies to target, monitor and resolve issues in the clinical trials/programmes Pilot the execution of the study from Study concept to final report Oversight of budgetary allocations Required skills; Minimum 1-year experience as Director of Clinical Operations Extensive Oncology knowledge and experience Thorough knowledge of first in man trials from phase 1-3 Clinical Trial design and execution Line management experience This is a permanent, office-based position. The successful candidate will be rewarded with a competitive basic salary and package. If this role is of interest, please send your CV to or call Clinical Professionals is a leading pharmaceutical staffing business. We have been placing professional within clinical research for over 10 years so have unrivalled knowledge of the market and can give tailored advice for you and outstanding levels of service throughout your career. We also have great relationships with our clients so pride ourselves on being able to identify clients that may be the perfect fit for you and bring you to their attention. By working proactively with candidates we find you the RIGHT job at the RIGHT time.

A fantastic opportunity for an experienced Regulatory Affairs Manager has become available within a leading Cell and Gene Therapy company based outside of London. They are looking to identify professionals with experience of ATMP, Orphan Drug or Biologics experience to join their growing team. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Regulatory Affairs Manager - ATMP will be varied however the key duties and responsibilities are as follows: 1. Contribute to regulatory strategy for Gene Therapy Products to support clinical development and approval of important therapies. 2. Prepare and write IMPD / IND submissions to EU and FDA markets. 3. Prepare Orphan Applications, PIPs, and PRIME submissions 4. Act as the point of contact for Regulatory Agencies including but not limited to the EMA, National Agencies and the FDA. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Regulatory Affairs Manager - ATMP we are looking to identify the following on your profile and past history: 1. Relevant degree in a life sciences discipline (e.e Biology, Genomics, Biotechnology etc.) ideally with experience of leading Cell or Gene Therapy development programs. 2. Proven industry experience in a Regulatory Affairs setting where you are contributing to dossier content and strategy. Experience of ATMPs is ideal but experience of Orphan Drug products and Biologics will also be of interest. 3. A working knowledge and practical experience with clinical development of ATMP technologies is a benefit. Key Words: Cell Therapy | Gene Therapy | Cell and Gene Therapy | ATMP | Biologics | Regulatory Affairs | IMPD | IND | CTD | MAA | EU | FDA | PIP | PRIME | Orphan Drug | Strategy | Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.

Overview of the role An experienced Post-Doctoral Scientist is required to conduct research within Circadian Therapeutics, Co-Founded by Professor Russell Foster (Head of the University of Oxford Nuffield Laboratory of Ophthalmology and Director of the University of Oxford Sleep and Circadian Research Institute), Associate Professor Aarti Jagannath (BBSRC David Phillips Fellow within the University of Oxford Sleep and Circadian Research Institute), Dr Sridhar Vasudevan (BBSRC-Royal Society of Edinburgh Enterprise Fellow within University of Oxford Department of Pharmacology), and Professor Maarten De Vos (University of Oxford Institute of Biomedical Engineering). The company works to understand the molecular control of circadian rhythms, enabling development of unique therapeutics to treat serious diseases associated with disruption of the body clock. The project involves leading a jointly-funded collaboration between Circadian Therapeutics (CT) and the Blind Veterans UK. The Blind Veterans UK is a charity that provides free support and services to Vision Impaired ex-Armed Forces and National Service personnel. One of the ways it does this is by awarding grants to organisations and groups that meet its priorities, criteria and conditions. CT is developing several molecular targets for circadian rhythm modulation that could result in new and more effective medicines becoming available for patients with sleep and circadian rhythm disruption. Blind Veterans wishes to contribute by way of a grant to the funding of a program of research to be carried out by CT and its academic collaborators. The post-holder will lead The Sleep and Circadian Health Research Program to develop new techniques of circadian estimation for application in diagnosis and delivery of circadian therapeutics in clinical and public health settings. This position requires the implementation of existing and developing new scientific techniques to quantify circadian phase in a patient sample of visually impaired individuals with circadian disorders. Additionally, the program must include circadian characterisation and phenotyping of all beneficiaries of the Blind Veterans UK as these phenotyped individuals, with an appropriate diagnosis and symptomatology, may in future become candidates for enrolment into the first interventional clinical study that CT will sponsor. The post holder will be required to liaise directly with the Blind Veterans UK Head of Research and Innovation. The post holder will also provide supervision and guidance to junior Post-doctoral fellows, research assistants, technicians, and PhD and project students. The position will require travel and stay for prolonged periods at test locations (South England and North Wales). Night shift work may also be required for adequate running of study procedures. Responsibilities/duties Development and management of the Sleep and Circadian Health Research Program, including the development of research objectives and hypotheses in collaboration with study investigators, management and implementation of research testing, and interpretation and analysis of research findings. Management of grant funds, including the acquisition of required equipment and hiring of junior staff. Development and implementation of standard operating procedures, adapting existing and developing new scientific techniques and experimental protocols, and responsible for ensuring quality control of all data. Act as a source of information and advice to other members of the team on specialised methodologies, protocols and experimental techniques. Direct and supervise junior staff including post-doctoral fellows, research assistants, project volunteers, and Blind Veterans Centre staff. Liaise directly with Blind Veterans UK Head of Research and centre staff to coordinate the research program with the Blind Veterans UK framework. Engage with local and/or international research collaborators to fulfil any unmet need of the project. Facilitate communication and collaboration between Circadian Therapeutics and Blind Veterans UK. Report on the Sleep and Circadian Health Research Program at monthly Circadian Therapeutics Operations meetings, and at Circadian Therapeutics and/or Blind Veterans UK Board meetings when/if required. Coordinate multiple aspects of work to meet deadlines Contribute to writing bids for research funding Collaborate in the preparation of scientific reports and journal articles and present papers and posters. Represent the research group at external meetings/seminars Selection Criteria: Essential Hold a relevant PhD in sleep and circadian medicine, together with specialist experience and expertise in assessment and measurement of circadian rhythms and insufficient sleep. Minimum of 3 years post-doctoral research experience Previous experience in leading industry-academic engagement project, including development and management of project objectives and staff, and financial planning and monitoring experience. Previous experience in preparing research grant applications (public and private) Experience of independently managing a discrete area of a research project and manage own academic research and associated activities Previous experience of contributing to publications/presentations Ability to contribute ideas for new research projects and research income generation Excellent communication skills, including the ability to write for publication, present research proposals and results, and represent the research group at meetings Experience of actively collaborating in the development of research articles for publication Desirable Previous experience in circadian research in both laboratory and field environments Previous experience working with sleep and circadian disorder patient groups Previous experience in circadian omics research Previous experience working with charitable organisations CLOSING DATE FOR APPLICATIONS 22 NOVEMBER 2018 NO AGENCIES PLEASE

Your new company This role will give you an opportunity to be part of a patient-centred organisation that has been around for 30 years whose main aim is to contribute to improving the lives and health of patients in the UK. It is a well-established, global biopharmaceutical company located in Cambridgeshire. Your new role As a Pharmacovigilance Compliance Specialist, you will be responsible for coordinating the planning, conduct and follow up of internal and external audits and inspections. You'll maintain knowledge of PV regulations. In this role you will be able to work closely with the quality team, as well as the pharmacovigilance team. This opportunity will also give you an excellent chance to develop more leadership responsibilities through training. What you'll need to succeed You will preferably hold a Bachelor's degree or equivalent in in a scientific discipline, as well as having relevant industry experience within pharmacovigilance, quality or compliance. Additionally, for this job you will have working understanding or global PV regulatory requirements and UK requirements too. You will be able to work effectively within a team whilst being able to work independently. What you'll get in return As a pharmacovigilance compliance specialist you will receive a competitive salary as well as benefits and bonus. You will be able to work within a leading global organisation, which will give you numerous responsibilities as well as excellent career progression opportunities. What you need to do now if you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Catherine Almond. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.