1 to 25 of 53 Permanent GMP Jobs

degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience working in Quality Assurance, GMP manufacturing environment, pharmaceutical environment, or medical device space Experience supporting quality activities in medical devices, combination products, pharmaceuticals, or another highly regulated industry. Working knowledge ...

plastics, including Regulation (EU) 2022/1616, Regulation (EC) 1935/2004, Regulation (EU) 10/2011, BRCGS for food-contact packaging materials and GMP requirements (EC) 2023/2006 Ensure the recycling process remains authorised and operates within any applicable EFSA opinion/Commission authorisation Design and maintain robust ...

feedback, championing continuous improvement, automation and a customer focused support culture. Profile description: We are looking for: Proven experience supporting enterprise IT infrastructure and GMP-regulated computerised systems within a regulated environment. A degree in a relevant field or HNC/HND would be advantageous. Strong technical knowledge of operating ...

working with food safety and quality management systems within a manufacturing or supply chain environment Confidence carrying out audits, inspections and compliance checks (e.g. GMP, hygiene, food safety) The ability to interpret technical data and communicate it clearly to a range of stakeholders Strong relationship-building skills across operational ...

identifying opportunities to deliver practical and lasting improvements. What you'll be doing Strengthen compliance: lead the continued development of our Food Safety, HACCP, GMP and BRCGS systems and maintain audit readiness. Build on our H&S culture: develop our existing Health & Safety systems, ensuring risks are well managed ...

Coordinate & take part in internal and external design reviews, DQ, HAZOP and site meetings where required. · Author, review and be responsible for project lifecycle GMP/validation documentation – technical writing is a core skill. · Contract management – clearly understand the commercial aspects of each assigned project and liaise with contract managers ...

management. About You: Essential: Experience in a quality management role within feed manufacturing, food production, or a similar regulated industry. Strong knowledge of HACCP, GMP, and quality management systems. Experience managing audits and regulatory compliance. Excellent leadership, communication, and organisational skills. Budget management and commercial awareness. Desirable: Experience with UFAS ...

Oriented Programming Git version control Basic electrical, mechanical and pneumatic knowledge Robotics Machine Vision SCADA/MES systems Pharmaceutical or regulated manufacturing environments GAMP, GMP, 21 CFR Part 11 or EU Annex 11 Industrial communication protocols including EtherCAT, Profinet, CAN, Ethernet/IP and Serial communications .NET ...

embedding Greencore, customer, and legal standards, ensuring compliance is consistently achieved and maintained. This role plays a critical part in driving improvements in GMP performance and audit readiness, helping to raise quality standards and strengthen food safety culture across the site. Role Accountabilities Understand and apply Greencore, customer ...

Experience working within pharmaceutical, medical device or regulated manufacturing environments would be advantageous. Knowledge of GAMP, 21 CFR Part 11, EU Annex 11 or GMP would be beneficial. Strong communication skills with the ability to work effectively within a team. A willingness to travel occasionally (typically less than ...

ability to sit office-based in the UK with periodic international travel. Desirable Direct experience managing US FDA regulatory interactions or GLP/GMP study programmes. Formal PM qualifications (PMP, PRINCE2, APM). Prior experience in a early-stage, venture-backed medical device startup. What they Offer High Impact ...

product standards. Work confidently around high-speed machinery, automated warehouse processes and manufacturing plant, including supporting basic fault finding and rectification where appropriate. Maintain GMP, hygiene, quality and audit standards within the warehouse, supporting checks, audits and follow-up actions as required. Share technical knowledge with team members to support ...

coach, develop and inspire technical teams. Desirable Experience within medical devices, healthcare technology or other safety-critical industries. Knowledge of IEC 62304, ISO 13485, GMP and FDA-regulated environments. Experience with cloud platforms such as Azure, AWS or GCP. Understanding of cybersecurity for connected devices and IoT systems. Exposure ...

laboratory environment and/or software development environment. Experience integrating instruments via serial/USB/Ethernet connections. Knowledge of Oracle databases. Understanding of GMP, GAMP or regulated software validation. Experience delivering customer training. Full UK driving licence. What we offer Career development and professional growth opportunities. Competitive salary. ...

leadership and development of Technical and Cancer Services. Your responsibilities will include supporting aseptic chemotherapy services, maintaining pharmaceutical quality systems, ensuring compliance with GMP, MHRA regulation and NHS standards, supervising and developing pharmacy staff, participating in clinical governance, audits and research, and supporting electronic chemotherapy prescribing systems. You will work ...

Master Data Specialist Role: Executing established Master Data Management processes in a GMP environment. Maintain data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems. Generate and approve standard Item Masters, Item Branches, and Item Revisions within JD Edwards. Raise required Change ...

Experience working in a manufacturing setting. Strong attention to detail and documentation skills. Understanding of regulated environments such as Medical Devices, Life Sciences, Pharmaceuticals, GMP, or ISO 13485 would be highly advantageous. Experience with incoming inspection, release testing, or supplier quality processes is desirable. This is an excellent opportunity ...

screens, pumps and piping, filters, heaters In house and client-based fault finding, rectification and diagnostics Supplier liaison Component-level testing and commissioning Cleanroom, GMP, This is a hands-on, varied position within a highly technical and fast-moving environment. Full training and instruction will be given and previous medical ...

Quality Assurance Officer (GMP/Cannabinoids) Sandwich Up to £40,000 + Company Bonus + Private Healthcare + Pension + Training Are you a Quality Assurance Officer or similar with GMP experience looking to join an innovative pharmaceutical manufacturer operating within one of the fastest-growing areas of the life … continued growth of a business operating in an exciting and evolving sector. This role would suit a Quality Assurance Officer or similar with GMP experience looking to broaden their technical expertise within a specialist pharmaceutical environment, where they'll have genuine responsibility, opportunities to influence quality systems and excellent prospects ...

meet operational targets; working with other functions to ensure mutual objectives are met. Compliance with Company policies, procedures and regulations (e.g. attendance, quality, safety, GMP’s, etc.) and ensure these are followed to maintain the required standards (e.g. Food Safety, PPE etc.). Resolve mechanical and/or electrical problems ...

BioLogics GmbH, a subsidiary of Gedeon Richter AG, is a dynamic, internationally established biotechnology company that develops and produces biopharmaceutical active pharmaceutical ingredients under GMP conditions with around 400 employees at its facilities in Hamburg and Bovenau. To strengthen our Business Development team, we are looking ...

similar role such as (multi skilled engineer, shift engineer, shift technician, engineering technician, electrical maintenance engineer) Knowledge of FMCG processes and experience working to GMP standards. Ability to work independently and as part of a team. Should this be of interest, please either apply or email (url removed ...

GMP Recruitment are proud to be in partnership with a highly recognisable, leading manufacturer located in Droitwich. We are currently recruiting on their behalf for someone to join their team as a Service Engineer on a full time, permanent contract. Up to £40,000 + Excellent Benefits + Extensive Worldwide ...

Responsibility QMS Governance & Compliance * Support the QMS Manager in the governance, development and ongoing maintenance of Veeva Quality. * Ensure QMS processes remain aligned with GMP, GDP and applicable global regulatory requirements. * Support periodic review of quality processes and system effectiveness. System Administration * Support configuration change requests through approved change control … technical communicator.Strong stakeholder management. Excellent interpersonal and influencing skills. Data analysis and interpretation. Degree Level Educated or Equivalent experience. Experience with GxP, GMP and/or of working with Veeva Systems and Vaults (desirable). Experience of working in a pharmaceutical environment (desirable, not essential). Additional Information: Occasional global ...

strategy, ensure inspection readiness, maintain licences, and deliver continuous improvement across quality systems and operations. The role is critical in ensuring compliance with GMP/GDP standards, supporting upcoming projects such as implementing an electronic QMS, and driving a culture of collaboration and high performance within the Quality function. … risk-based decision-making. Operational Excellence Support change-control processes and ensure timely resolution of quality issues. Oversee approval and maintenance of SOPs and GMP-related documentation. Always ensure inspection readiness for MHRA and customer audits. Team Development Manage QA and QC teams (approx. 16). Build a nurturing ...