About the Role
QA Manager – Projects and NPI Support. Lead a team of QA Specialists supporting site projects, new product introductions (NPI), and technology transfer programmes within a GMP‑regulated pharmaceutical manufacturing environment. This role is critical in ensuring quality is embedded throughout the project lifecycle, from design and qualification through to commercialisation, while maintaining full compliance with EU GMP requirements and industry best practices.
As the primary QA representative within project governance structures, you will provide expert leadership in quality risk management, validation, change control, and quality systems oversight. Working closely with cross‑functional teams including Engineering, Production, QC, Supply Chain, and Project Management, you will ensure project objectives are delivered efficiently without compromising quality, compliance or patient safety.
In addition to leading and developing a high‑performing QA team, you will drive continuous improvement initiatives, support regulatory inspections and audits, and play a key role in the successful introduction of new products and technologies. This is an excellent opportunity for a quality professional who enjoys influencing strategic projects, building strong stakeholder relationships, and fostering a proactive quality culture within a fast‑paced manufacturing environment.
This team‑lead role requires effective day‑to‑day leadership, supervision and development support for the expanding QA team, ensuring appropriate oversight, prioritisation and compliance management across all activities.
Responsibilities
- Lead QA team in managing QA activities for projects, NPI and technology transfer.
- Oversee quality risk management, validation, change control and quality system oversight.
- Collaborate with Engineering, Production, QC, Supply Chain and Project Management teams to meet project objectives.
- Drive continuous improvement initiatives and support regulatory inspections and audits.
- Ensure compliance with EU GMP requirements and industry best practices throughout project lifecycle.
Qualifications
- Experience as a QA Projects Manager or similar role in a GMP‑regulated pharmaceutical manufacturing environment.
- Strong knowledge of EU GMP, validation, change control and quality risk management.
- Ability to lead and develop a high‑performing QA team.
- Excellent communication, stakeholder management and problem‑solving skills.
Benefits
- 25 days holiday + bank holidays
- Buy/Sell Scheme
- Generous employer pension contribution
- Private medical, dental and permanent health insurance
- Group life assurance
- Free will writing services
- Active well‑being programme
- Recognition awards
- Free parking
Location
Holmes Chapel, Cheshire – a beautiful village with excellent transport links via railway and motorway network, proximity to Manchester Airport, and near the National Parks of the Peak District, Lake District and Eryri.
EEO Statement
We value our inclusivity and aim to celebrate diversity. We are a disability positive employer and will support you throughout the recruitment process with any adjustments you require.
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