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 ❯
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 ❯
with completing product checks (organoleptic, viscous testing, weight checks etc) and where necessary, complete daily paperwork. Verify finished product labels and case end labels to ensure correct dates. Complete GMP & Hygiene Audits. Complete of Daily/Monthly/Quarterly Glass & Hard Plastic Audits. Verification of line cleaning. Micro sampling to site schedule and manage an ongoing shelf-life library of 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 ❯
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 ❯
regulated manufacturing environment. This opportunity is ideal for someone with a science or pharmaceutical-related degree and exceptional people management skills, looking to make a meaningful impact in a GMP-licensed facility. Key Responsibilities: Lead and manage a team of QA Officers to ensure product release meets GMP and QMS standards. Support the QA Manager with site inspections, internal audits … risks are mitigated. Experience: Degree in Microbiology, Biology, Biomedical Sciences, or equivalent. Pharmacy Technician Level 3 (GPhC registration desirable). Proven experience in pharmaceutical manufacturing and working within a GMP-regulated environment. Strong leadership and coaching skills with a track record of team development. Excellent understanding of MHRA regulations, ISO standards, and quality systems. Skilled in risk management, root cause More ❯
of Solstice. Key Responsibilities Monitoring ongoing compliance with food safety, legislation, quality & customer requirements, and industry regulatory requirements. Interpret and implement quality assurance standards and procedures. Monitor and promote GMP, Hygiene, Quality Standards, and adherence to all Quality Management & Food Safety related procedures. Managing Microbiology testing schedule, including product samples and environmental swabs collections Conducting and document internal audits (GMPMore ❯
