1 to 25 of 53 Permanent GMP Jobs

automation systems in an FDA-regulated environment. Hands-on experience with serialization, track & trace, or vision inspection systems (Systech preferred, other platforms welcome). Background in control systems within GMP manufacturing (pharma, biotech, or food highly relevant). Ability to troubleshoot complex systems, lead root cause analysis, and implement CAPAs. Strong knowledge of PLCs, industrial controllers, instrumentation, and network design. More ❯

teams. ?? Support change management and training initiatives to ensure smooth adoption of new tools and processes ? Ensure all business processes and documentation comply with FDA, ISO, EU MDR, and GMP standards. ?? Qualifications & Experience ?? Bachelor's degree in Engineering, Supply Chain, Business, Data, IT , or a related field. ?? 10+ years' experience as a Business Analyst within manufacturing, supply chain, medical devices More ❯

with diverse cultures Necessary legal status to work in the UK. Beneficial requirements: The closest relevant experience would be MES/EBR, eQMS, LIMS, ERP or other systems for GMP regulated manufacturers. Experience of different project delivery methodologies including waterfall and agile Experience of client account management Knowledge of Computer System Validation is an advantage. Key Responsibilities: Become an expert More ❯

understanding of the business. Experience of working in a pharmaceutical manufacturing operation is desirable. Responsibilities · Conduct validation activities for Lab systems in accordance with Quality Standards and Practices and GMP guidelines · Initiate and implement Change Control activities for existing quality systems in accordance with Quality Standards and practices · Resolve validation issues, incident problems and deviations using data analysis and problem More ❯

capture and patent support. Consistently demonstrate a strong commitment to both lab and process safety. Adhere to and promote biosafety, hygienic design and quality management standards (e.g. BSL-2, GMP, FSMA, HACCP, ISO food-grade). What you can bring to the role Ideally PhD qualified in Biochemical Engineering, Biological Engineering, Fermentation Engineering, or a related technical degree. Proven industry More ❯

and embedded analytics for production KPIs. Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable. Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.). Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs. Ability to translate complex operational processes into streamlined SAP-enabled solutions. More ❯

and embedded analytics for production KPIs. Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable. Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.). Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs. Ability to translate complex operational processes into streamlined SAP-enabled solutions. More ❯

to succeed: Proven experience as an Analyst within a pharmaceutical or manufacturing setting. Strong data analysis skills with advanced Excel and reporting tools (e.g., Power BI). Knowledge of GMP/GDP and regulatory documentation requirements. Ability to identify and resolve data discrepancies across systems, with a willingness to learn and apply SAP processes where required. Excellent communication skills for More ❯

a scientific discipline (e.g., microbiology, biology, biomedical sciences) or equivalent. Proven experience in quality assurance within a regulated manufacturing or laboratory environment. Strong knowledge of quality systems, ISO standards, GMP/GDP principles, and regulatory compliance. Skilled in leading audits, managing CAPAs, and interpreting quality metrics. Excellent leadership, communication, and problem-solving abilities. Proficient in data analysis tools, LIMS, and More ❯

Candidate: Proven experience in a quality systems or quality assurance role within a manufacturing or production environment - precision environment Strong knowledge of quality standards and regulations such as ISO, GMP, FDA if applicable). Experience with quality tools and methodologies such as CAPA, FMEA, Root Cause Analysis Certification in quality management systems - desirable Excellent communication, analytical, and problem-solving skills. More ❯

A minimum of ten years' 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 science project delivery Knowledge/ More ❯

data platforms) Understanding of data governance and compliance (ideally obtained from a highly-regulated environment) Excellent problem-solving skills and attention to detail Preferred Qualifications: Knowledge/experience of GMP would be highly advantageous. Benefits: Competitive base Salary Annual bonus based on company performance Opportunities to partake in on the job training courses Opportunities to attend and participate in industry More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

solve we would like to hear from you. Full training on internal quality processes is provided to the successful candidate. Role Accountabilities: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and necessary corrective action - then following More ❯

integration technologies (OData, REST APIs, IDocs), plus knowledge of manufacturing automation protocols (OPC UA, MQTT). - Prior experience in regulated manufacturing industries (e.g., Pharmaceuticals, Medical Devices) with understanding of GMP/FDA validation requirements, and expertise in developing compliant solutions within SAP environments. Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status More ❯

packaging and goods-in areas in the event of staff shortages Address non-conformances and corrective actions immediately Handle customer complaints and supplier NCRs Weekly Duties Probe & scale calibration GMP audits (3–4 per week) Staff induction, manual handling, and refresher training Machinery and health & safety training with supervisors Traceability and raw material paperwork checks Forklift, cleaning, and first aid More ❯

resolving day to day issues/escalation points. How Will You Make An Impact? Ensuring a safe, clean, and good working environment by utilising 5S principles, implementing and monitoring GMP standards, and ensuring compliance with Arlas standards in terms of Food Safety, Health & Safety, and Environment, including conducting internal audits. Assisting the team to achieve their objectives through training, coaching More ❯

looking for a QA Manager to join their Technical team. In this QA Manager position you will lead the QA team and be responsible for delivering high levels of GMP, food safety and integrity standards within the factory. You will also be responsible for updating and maintaining the QMS, conduct audits and ensure any corrective actions are implemented. As the More ❯

applications and embedded analytics for shop floor and KPI reporting. Advantageous: exposure to IBP, PP/DS, or advanced scheduling tools. Awareness of manufacturing standards and compliance (e.g., ISO, GMP). Soft Skills & Leadership Strong communication and stakeholder management, particularly with operations, production, and executive-level teams. Ability to translate complex business processes into practical SAP-based solutions. Confident presenting More ❯

changes in direction. Ability to work in a team environment. Demonstrate initiative; be proactive, responsible, and self-managed in relation to tasks. cGMP experience is highly desirable. Familiarity with GMP systems such as LIMS, MES, automation, and historian software is desirable. Well organized, detail-oriented, and adaptable to changes. More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

checks, supplier and internal non-conformance, customer complaint investigations, glass & plastic audits, and fabrication audits. - Supporting the training of staff and verification against CCPs, policies and procedures. - Conducting internal GMP audits across departments and conducting hygiene verifications. - Assisting with external audits. The role will be a mix of factory and office-based work to meet the needs of the business More ❯