101 to 125 of 129 Permanent GMP Jobs in England

in a multi-talented and compliance orientated team. You have · A background in a scientific discipline (MSc is a plus) · Experience working within a GMP environment, preferably in a CDMO · Strong experience of QC environment and organisation · Experience of reagent preparations and material handling Touchlight Benefits Touchlight is a successful more »

on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated more »

bench to bedside concept.Working under the trusts Pharmaceutical Quality System, the post holder will use their experience and specialist knowledge in Good Manufacturing Practice (GMP), immune cell culture, immune cell purification by high end multicolour flow Cytometry and or other methods to take responsibility for developing and delivering the manufacturing … expansion. Required to work with collaborators in developing processes by taking pre-clinical ideas and technology transferring to the unit and ensuring phase appropriate GMP compliance Lead Validation and qualification procedures for processes and equipments used for manufacture of immune cell products3 Provide specialist knowledge of the latest developments within … implementing independently controlled documents: Investigational Medicinal Product Dossiers, Product Specification Files, Batch Manufacturing Records and Standard Operating Procedures (SOPs) for Production activities in the GMP unit. Ensure adequate maintenance and supervision of equipment, and ensure compliance with Planned Preventive Maintenance (PPM) Undertake strategic judgements based upon specialist knowledge of the more »

build brighter futures for colleagues, clients and communities. The role will form part of the projects team with the current focus being around delivering GMP Equalisation projects on the proposition to clients, which can incorporate or lead onto being involved in de-risking projects for clients over time. This is … with internal teams to deliver a streamlined service to other lines of business. Directly involved with the management of more junior colleagues within the GMP Equalisation team, including supporting with performance reviews, training, and personal development plans. Develop skills to support on various consulting aspects of GMP projects and have … in Pensions, with a focus on Technical aspects and solid exposure to consultants and broader client support teams. Experience of technical calculations required for GMP Rectification and Equalisation projects. more »

responsibility will be to ensure that all materials are tested according to agreed specifications and procedures, in agreed time frames and in accordance to GMP and company guidelines. Other key responsibilities will include to: - Qualify, maintain and calibrate all laboratory equipment according to procedures. - Maintain all laboratory Quality Systems and … Assurance Performance Indicators. Your Background: You are required to have the following qualifications, skills and experience: - Knowledge of Quality Control, Quality Assurance, Quality Systems, GMP and basic understanding of manufacture and packaging of pharmaceutical products. - Stability testing experience - Hands-on HPLC experience - Good technical and scientific judgement. - Diplomatic, self-motivating … professional with problem solving and decision-making capabilities. - Basic understanding of GMP Guidelines and Regulations. Apply: For more information, or to apply for this QC Analyst position please contact Hannah Oakley on 01246 457711 or email hoakley@ckgroup.co.uk. Please quote job reference 56706 in all correspondence. It is essential that more »

x2). You will also get 25 days holiday and an enhanced pension. The role is to support production and manufacturing tasks working to GMP (good manufacturing practices) . The Role: Permanent, full time position working mainly days and occassional nights as a General operative within manufacturing Various production tasks more »

PhD or relevant degree in any chemistry or life science related subject. The ideal candidate will have previous experience of working to GLP/GMP Must be IT literate with competent use of the Microsoft systems. The ideal candidate will have previous experience of using LC-MS/MS. Previous more »

ABOUT YOU Are you a Quality professional with experience in a GMP laboratory, looking for a role that will challenge you, and help you develop new skills? You will possess rigorous attention to detail and be hungry for a challenge out of the lab. We need you to have: BSc …/MSc/PhD in Chemistry (or related scientific discipline) A sound working knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry Quality Assurance background which includes some specialist knowledge within a defined … Excellent attention to detail Impressive written and verbal communication ABOUT THE OPPORTUNITY You will provide general support to Quality Assurance activities relating to GLP, GMP, GCP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved. more »

engineering or similar. Substantial demonstrable experience leading a company through ISO9001/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality management" within a technology company including instilling a quality-focused culture and maintainable approach more »

Job summary This position presents an exciting opportunity for an experienced radiochemist or radiopharmacist proficient in PET radiopharmaceutical production to GMP standards. As the Production Manager, you will lead our team of radiochemists at the Positron Emitting Radiopharmaceutical Laboratory (PERL), located within St Thomas Hospital. The ideal candidate must possess … expert knowledge in relevant regulatory governance areas, particularly Good Manufacturing Practice (GMP), as well as Health and Safety, Environmental Safety, and Radiation Protection Regulations (IRR2017 and IR(ME)R). This expertise will ensure adherence to these regulations within the PERL facility. Main duties of the job The role entails … managing radiochemists within PERL to ensure timely, safe, and efficient completion of production duties. Emphasis will be placed on compliance with GMP regulations, development of new procedures and radio tracers, and streamlining processes while maintaining safety standards. This includes supporting the installation and validation of new production equipment. The successful more »

risk assessments Experience of participating in audits/internal monitoring Desirable Knowledge of regulatory requirements relating to clinical trials Awareness of Good Manufacturing Practice (GMP) inc Annex 13 labelling requirements Personal/Professional attributes Essential Excellent attention to detail. High level of initiative Able to problem solve Able to work more »

trial design, to advise them on good practice in accordance with the International Conference on Harmonisation (ICH) guidelines on Good Clinical practice and Good Manufacturing Practice and on the regulatory status of the clinical trial drug. 5. To lead and finalise the set-up of cancer clinical trials, i.e. writing … years post-graduate training above original Masters level qualification) Vocational Masters degree in Pharmacy (4yrs) and 1 years pre-registration training and experience) GMP accredited Desirable Specialist qualification in cancer therapy or equivalent knowledge Qualified Independent Prescriber or willing to undertake training Experience Essential Substantial post registration experience in a more »

least 3 years industrial experience and be able to work on a number of product development projects. Previous industrial experience within a regulated environment GMP environment, pharmaceuticals, food, electronics . Demonstrate project control, with evidence on how you achieved the business goal. Provide support to design operatives to aid in more »

correctly. Ensure that the aseptic process is carried out in compliance with current Standard Operating Procedures following the principles of the Good Manufacturing Practice (GMP). About us Liverpool University Hospitals NHS Foundation Trust was created on 1 October 2019 following the merger of two adult acute Trusts, Aintree University … correctly. Ensure that the aseptic process is carried out in compliance with current Standard Operating Procedures following the principles of the Good Manufacturing Practice (GMP). See Job Description for further information. Person Specification Experience Desirable Experience working in Healthcare Environment Experience of stock rotation Experience of working in stores more »

role for you! As a Technical & Quality Coordinator, you will be: Updating and developing technical documentation. Ensuring the organisation remains compliant with food safety, GMP, quality, ACCP , and health and safety procedures . Conducting, and supporting with, internal and external audits and finished product traces . Recording all findings and … in food science or related field. Previous experience in a Quality & Technical role within food manufacturing . A strong understanding of HACCP, BRCGS, and GMP standards and food legislation . Computer literate with MS Office. Able to work well independently and part of a team. If you believe you meet more »

clinical trials and practice research. Experience of supervision of staff. Experience in delivering training and education to staff. Understanding of the principles of Good Manufacturing Practice and Quality Assurance Understanding of Section 10 exemption of the Medicines Act and the requirements that this brings Understanding of Good Clinical Practice and … Band 8a - Sound understanding of the principles of Oncology/haematology Band 8a - Evidence of delivering service improvements. Band 8a - Working knowledge of current GMP and QAAPS standards and legislation. Band 8a - Enhanced knowledge of Good Clinical Practice and experience of handling clinical trial material (IMP) in an aseptic unit. more »

a Quality Director to head up a Quality department. The Quality Director will promote and integrate quality into every aspect of the business ensuring GMP compliance and meeting the authority's expectation. The role holder will perform all duties required of a Quality Director, provide leadership to the Quality Teams … the business and provide support to sister company for regulatory inspections and conduct self-inspection program Oversee the Pharmaceutical Management System. Implement the current GMP regulations and industry best practices, where applicable Support and develop the QA team Support/lead manufacturing deviation or testing out-of-specification/out … of-trend investigations Audit the contract manufacturing organisation and laboratory against EU GMP and relevant regulations and guideline Qualifications and Skills: Qualified Person (QP) Knowledge and experience in manufacturing and testing of oral dosage forms and topical products Experience in releasing medicinal products in a fast-paced environment Experience in more »

The site Head of Quality will lead the designated site in terms of GMDP quality and compliance, including in the areas of: QA, QC, GMP, GDP, QP activities and RP activities in line with the business goals and plan. Responsibilities: Establish clear and compliant GMDP standards for all site activities more »

experience leading IT at a senior management level • Track record of delivering results quickly • Experience in delivering IT services to customers • Work in a GMP or highly regulated environment Preferred Experience: • Experience of agile product development • Experience of Lean Six Sigma • Infrastructure delivery (networking, hardware) to customers • Experience with data more »

Comfortable operating autonomously once goals and objectives are set. Excellent interpersonal, written and verbal communication skills. Confidence and ambition to provide pragmatic and considered GMP advice. Having current and up to date professional knowledge, expertise and best practice. Proven ability to engage constructively with colleagues at all levels across different more »

of pharmacist as required3.Participation in screening, dispensing and checking of clinical trial prescriptions, and advising others of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and requirements relating to Investigational Medicinal Product (IMP) management.4.To participate in the Trust-wide Out of Hours Medicines Advice Service and seven-day medicine supply more »

The Role - Development/GC MS/HPLC Scientist The Salary - Competitive The Location - Yorkshire Russell Taylor group has a brand-new opportunity for a chromatography scientist. If you think this role would be of interest, apply now to avoid more »

+ 8 Bank Holiday Cycle to Work Scheme Skills and Qualifications Required for Analyst BSc or higher in Chemistry or related field Experience within GMP environment Physical characterisation including; particle sizing (image and laser diffraction), specific surface area, XRD, thermal analysis, water content Chemical ID analysis including; UV-vis, FTIR more »

with our long standing client in Bristol at an exciting time in their business where they will be commissioning a new Good Manufacturing Practice (GMP) facility. This will be in a new building and be a blank canvas for the new Quality Assurance and Validation Engineer to work on! You … will be working with colleagues both internal and external on commissioning and qualification of this new GMP facility. This will include equipment IQ/OQ/PQ activities, as well as validation and qualification of the ISO 7 and ISO 8 cleanrooms. You will be responsible broadly for all systems … self motivated with a can-do approach. Your background: Bachelors Degree in science or engineering with experience in facilities and equipment validation. Experience of GMP manufacturing, facilities, equipment qualifications and process validations, including cleanrooms. Knowledge of cGMP manufacturing regulations for the MHRA, FDA and other countries as required. Experience in more »

maintained and up to date. Education and experience : *Degree in chemistry, analytical chemistry or equivalent *Previous experience of HPLC, GC analysis with pharmaceutical/GMP regulated environment *Previous experience in analytical method transfer, cleaning validation *your previous experience could be QC analyst, stability analyst, development analyst, principal analyst and raw more »