We are currently supporting a global pharmaceutical manufacturing group with the identification of an experienced MSAT professional to support current and future projects within their Oral Solid Dosage (OSD) operations.
This opportunity would suit a hands-on MSAT consultant who thrives in fast-paced GMP environments and enjoys working across tech transfer, process optimisation and manufacturing scale-up activities.
Key Responsibilities
* Provide MSAT support across OSD manufacturing (tablets, capsules, granulation, compression, coating).
* Lead and support process engineering activities including troubleshooting, optimisation and continuous improvement.
* Play a key role in tech transfers, PPQ, scale-up and site integration projects.
* Drive CPV implementation and data-led performance monitoring.
* Partner closely with Production, Quality, Validation and Engineering teams to stabilise operations and improve right-first-time performance.
* Support equipment lifecycle management, including FAT/SAT, CQV and ongoing reliability improvement.
What we are looking for
* Strong background in MSAT or Process Engineering within pharmaceutical manufacturing.
* Proven hands-on experience in OSD dosage forms (solid oral manufacturing).
* Track record of delivering in GMP-regulated environments.
* Experience across tech transfer, validation, PPQ and scale-up phases.
* Confident working cross-functionally in complex, matrix organisations.
* Comfortable operating in high-pressure manufacturing environments.
* Upstream & Downstream experince
Charles Wiltshire
cwiltshire@barringtonjames.com
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