MSAT Manager: Drug Substance Process & Tech Transfer Leader

Allerton Bishop Search; Greater London; On-site; GBP 80,000 - 110,000; Full time

Job summary

Allerton Bishop is partnering with a London-based speciality pharmaceutical company to appoint an experienced MSAT Manager. The MSAT Manager will provide technical oversight of drug substance development and manufacturing activities, working closely with external CDMO partners across both clinical and commercial programmes.

The role will cover process development, scale-up, technology transfer and lifecycle management, working cross-functionally with CMC, Quality and Regulatory teams.

Qualifications

• MSc or PhD in Chemistry, Chemical Engineering, Pharmaceutical Sciences or related.
• Experience in pharmaceutical drug substance/API development or manufacturing.
• Strong MSAT experience in process development, scale-up, technology transfer or CMC.
• Experience managing CDMO/CMO relationships across clinical and commercial manufacturing (Desirable).
• Understanding of GMP, CMC and regulatory requirements for drug substance manufacturing.

Responsibilities

• Provide technical oversight of drug substance development and manufacturing across clinical and commercial programmes.
• Lead the technical relationship with CDMO partners, ensuring delivery to quality, technical and timeline requirements.
• Manage process development, scale-up and technology transfer from laboratory through to commercial manufacturing.
• Provide MSAT input into CMC development strategies, regulatory submissions and lifecycle management.
• Lead technical investigations and manufacturing improvements in collaboration with external partners and internal stakeholders.

Skills

MSAT

Process Development

Scale-up

Technology Transfer

CDMO Relationships

GMP/CMC Knowledge

Education

MSc or PhD in Chemistry/Pharma

Job description

Allerton Bishop is partnering with a London-based speciality pharmaceutical company to appoint an experienced MSAT Manager. The MSAT Manager will provide technical oversight of drug substance development and manufacturing activities, working closely with external CDMO partners across both clinical and commercial programmes.

The role will cover process development, scale-up, technology transfer and lifecycle management, working cross-functionally with CMC, Quality and Regulatory teams.