1 to 25 of 165 Permanent GMP Jobs in the UK

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

policies. To be proactive in identifying and eliminating faulty processes by implementing long-term fixes. To uphold and exceed standards of product quality and GMP within their area that are appropriate to an industry-leading quality food manufacturer. To play an active role in the shift and be the go more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position: Carry out Daily/weekly GMP audits as required. To complete a detailed shift ... more »

your professional growth * Employee Assistance Program for holistic support KEY RESPONSIBILITIES: Quality Assurance Audit Program: Oversee all internal and external audits (Quality, Food Safety, GMP, Ethical Certifications, Customer) Create and manage the site audit calendar Support internal audits per BRC requirements Log and address non-conformances Collaborate to resolve audit more »

standards and key performance indicators. Support sensory activities: taste panels, sample preparation, sample collection, sample submissions, processing of results. Adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and master cleaning schedules (MCS). Comply with Company, third party and Customer standards demonstrated by successful completion of Inter-lab more »

and vision systems integrated within packaging equipment including interfaces with enterprise systems. Responsible for providing cGMP compliant control systems as per GAMP5 and EU GMP Annex 11. Key Experience Essential - Practical experience working within manufacturing and packaging environments Experience of the automation project lifecycle including design, configuration, implementation, testing, commissioning more »

company or CRO Experience on CMC documentation for respiratory devices is important Experience in Drug product development from early to late stage inclusive of GMP/clinical supply manufacture Experience with regulatory documentation for CMC activities on drug substance, drug product both towards FDA and EMA is mandatory Solid experience … with working in a regulated environment under GxP and with adherence to Company SOPs, policies and guidelines Updated knowledge of ICH GMP is required Excellent communication, presentation, and interpersonal skills. Self-driven and motivated team player Familiar with working in a virtual set-up Fluent in written and spoken English more »

Summary: The Head of Quality Assurance leads strategic QA efforts, ensuring compliance and driving improvement. They oversee operations, manage teams, and maintain high standards. Responsibilities: Define and drive QA strategy. Set and monitor quality standards. Ensure compliance with regulations. Lead more »

site and related functions in maintaining compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The individual will have support key quality system elements and compliance improvements, working closely with relevant stakeholders 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 »

related to the instruments You will produce timely and detailed reports for equipment Follow the companys procedures and policies as well as ISO and GMP standards on customer sites You will work closely with the technical team such as Field Application Specialist, Technical Sales Specialist, Technical Support Engineer and Sales … in a regulated environment, however training will be provided You may have field service experience working in the pharmaceutical, biological, or chemical industry following GMP or ISO standards in a similar role though candidates from other industries will also be considered (manufacturing, electronics etc.) Ability to work autonomously and unsupervised more »

site in Loughborough, you will be responsible for conducting chemical testing following set procedures, maintaining accurate records of work and conducting all analysis following GMP and/or internal procedures. This will include undertaking the chemical analysis of raw materials, intermediates and products according to set procedures and methods, as … environment. Experience in analytical techniques (UV, IR, KF, HPLC, GC and dissolution analysis). Previous experience with analytical method transfer and validation. Experience in GMP raw material testing for API, Excipients & packaging Experience in the use of LC-MS systems Experience of conducting cleaning validations and verifications Reward For the more »

vacuum cooler. Help with maintaining the plant to ensure we are hitting our consent. Ensure all maintenance equipment is fit for purpose. Compliance to GMP, QMS, 5'S, BRC Person Specification ONC in a related subject or equivalent experience Recognised apprenticeship Experience of working in an FMCG environment Electrical engineering more »

being made correctly Write reports on the analysis carried out for CofAs. Ensure that the testing done is carried out to the required standard (GMP, GLP, MHRA etc). What do you need to be considered? You will need: Degree or equivalent experience in science-based subject, ideally Chemistry. Working … Experience of analysing organic compounds such as fine chemicals, petrochemicals, or APIs. Knowledge of working in a regulated laboratory and standards such as UKAS, GMP, GLP, MHRA, FDA etc. What to do next? Interested? Of course you are, who wouldnt want to work for a great company with a supportive more »

cyclotron manufacturing processes to provide radioisotope for PET radiopharmaceutical production Ensure that the requirements of Cyclotron Preventative Maintenance, Radiation Compliance, Health and Safety, Good Manufacturing Practice and licensing commitments are met Perform manufacture of radioisotopes according to MarketingAuthorisationsand/or Specials license Be on call during the night for manufacturing … Experience in provision of PET radioisotope production for the commercial manufacture of PET radiopharmaceuticals Practical experience of working with ionizing radiation Working knowledge of GMP environment Benefits: 26 days' holiday with the option to buy or sell an additional 5 Up to 10% employer pension contribution Share and bonus scheme more »

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

focus on compliance within a specific bakery, working with the teams to identify non-compliance and full engagement and support to ensure company processes. GMP and procedures are fully understood. Work with the bakeries to ensure compliance with relevant customer standards and codes of practice. Conduct physical factory audits (outside … safety and quality. Ensure that the Quality Management System internal audit schedule is completed, and all actions closed out in a timely manner. Ensure GMP & QA CCP audits are conducted to schedule and any non-conformances raised to bakery management. Verify that close out actions are robust and complete. Communicate more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

to our customers through timely response and effective communication. * Ensuring Engineering standards are maintained, compliant with all legal requirements and factory standards and procedures (GMP, HSE and Process, etc.) are adhered to. * Liaise with department streams through meetings, understanding issues and setting plans to resolve. * Drive PPM's completion to more »

Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master more »

and maintenance of the company's Quality Management System (QMS) in accordance with regulatory requirements. Assist in conducting internal audits to assess compliance with GMP/GDP standards and company policies. Participate in the review and approval of GMP documentation, including batch records, SOPs, and change controls. Assist in deviation … Bachelor's degree in Pharmacy, Chemistry, or related field. Some experience or internship in a pharmaceutical quality assurance role is preferred. Basic knowledge of GMP/GDP regulations and quality management systems. Strong analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal skills. Ability to work more »

you will be responsible for testing and reporting laboratory activities to enable compliant, on time delivery of products to the customer whilst adhering to GMP standards. Your contribution will be the regular completion of on the bench testing of Asthma Inhalers (MDIs). You will be part of a quality more »

addition, this role may develop into encompassing the following: Promoting HACCP principles throughout the Group; Carrying out Internal Audits including UKAS (ISO 17025) and GMP audits as required; Assisting with the development and understanding of Food Hygiene Standards and Practices and GMP throughout the Group. Assisting with the development and more »

What you'll be doing: Lead on the delivery of assigned projects and scheme events Review the work of Pensions Data Technicians and provide feedback and technical support Regularly review the effectiveness and efficiencies of existing systems and controls and more »