Senior MSAT Specialist

Das ist der Job

Drive process scale-up, optimisation and validation for sterile drug product manufacturing.

Darum lohnt es sich

This is an outstanding opportunity to join a highly technical MSAT team supporting the development, transfer and commercial manufacture of innovative injectable medicines.

The Opportunity As a Senior Scientist within MSAT, you will provide scientific and technical leadership across the full drug product lifecycle, working closely with Manufacturing, Engineering, Quality and global project teams to deliver robust, compliant and scalable manufacturing processes.

Partner with Engineering, Manufacturing, QA and Development teams to support new product introductions. Strong communication skills with experience working across multidisciplinary and customer‑facing teams.

Competitive salary, comprehensive benefits and genuine long‑term career progression. #J-18808-Ljbffr Allerton Bishop is delighted to be partnering with a global pharmaceutical manufacturer to appoint a Senior Scientist – Manufacturing Science & Technology (MSAT) for its expanding sterile manufacturing operation in North Rhine-Westphalia , Germany .

The successful candidate will play a key role in technology transfers, process scale-up and process validation, with particular expertise in Pre-Filled Syringe (PFS) manufacturing. This is a hands‑on technical role combining shopfloor support with strategic process development, client interaction and cross‑functional project leadership.

Key Responsibilities Lead technology transfer activities from development through to clinical and commercial manufacturing. Provide technical expertise across Pre‑Filled Syringes (PFS), formulation, filling, assembly and packaging processes. Support liquid and lyophilised vial manufacturing technologies.

Develop process control strategies, risk assessments and process characterisation studies. Author and review technical protocols, validation documentation and scientific reports. Lead manufacturing investigations, root cause analysis and CAPA activities. Provide technical support during customer meetings, regulatory inspections and client audits.

Contribute to technology development, operational excellence and continuous improvement initiatives. Candidate Profile MSc or PhD in Pharmaceutical Sciences, Biological Sciences, Engineering or a related discipline. Experience within Manufacturing Science & Technology (MSAT) , Process Development, Technology Transfer or Technical Operations.

Strong knowledge of sterile drug product manufacturing. Good understanding of EU GMP and Annex 1 requirements. Experience supporting aseptic manufacturing, liquid filling and ideally lyophilised products. Why Apply? Join a global pharmaceutical organisation investing in sterile manufacturing excellence.

Work on innovative injectable products supporting patients worldwide. Gain exposure to complex technology transfers and commercial manufacturing projects. Highly collaborative environment with significant opportunities for professional development.