Key Responsibilities
- Lead and support a team of QC analysts/scientists, managing workload, priorities and day-to-day laboratory activities.
- Oversee QC testing across areas such as analytical, microbiology, biochemistry or molecular testing, depending on the laboratory.
- Ensure all testing is performed in accordance with GxP, GMP, SOPs and regulatory requirements.
- Review and approve analytical data, results, deviations, OOS/OOT investigations and laboratory documentation.
- Support method validation, method transfer, equipment qualification and laboratory investigations.
- Work closely with QA, R&D, Manufacturing and other technical teams to resolve quality issues and maintain compliance.
- Identify opportunities to improve laboratory processes, systems and efficiency.
- Support the implementation and use of laboratory systems, including LIMS, where required.
- Coach and develop team members, ensuring appropriate training and competency are maintained.
- Contribute to audits, inspections and continuous improvement initiatives.
Key Requirements
- Previous experience leading a QC laboratory team within a pharmaceutical, biotech, medical device or other regulated environment.
- Strong knowledge of GMP/GxP and QC laboratory processes.
- Experience with investigations, deviations, OOS/OOT and CAPA.
- Understanding of analytical testing, laboratory systems and data integrity.
- Strong leadership, communication and stakeholder-management skills.
- Experience working with LIMS or other laboratory informatics systems would be advantageous.
- Relevant scientific degree or equivalent laboratory experience.
- Ref:
- 52866
- Market Specialism:
- LIMS