MSAT Lead: Vaccine Platform & Tech Transfer

Barrington James

Pennsylvania

On-site

USD 150,000 - 190,000

Full time

14 days+

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Job summary

Barrington James is seeking an MSAT Lead for a global biopharmaceutical manufacturer undergoing site transformation, to lead a 4-6 member MSAT team and contribute as a hands-on technical resource for process troubleshooting and lifecycle management.

You will partner with upstream/downstream teams and international sites, support drug substance and drug product tech transfer as new facilities come online, and ensure GMP compliance and readiness for inspections.

Qualifications

  • Bachelor's degree in a relevant field with 8+ years in MSAT or pharma/biotech.
  • Experience leading or managing a team.
  • MSAT experience with Drug Substance and Drug Product preferred.
  • Hands-on experience with UFDF and chromatography.

Responsibilities

  • Lead and develop a team of 4-6 technical specialists supporting MSAT activities.
  • Provide in-depth technical expertise across process validation, troubleshooting, and optimization for drug substance manufacturing.
  • Support lifecycle changes and impact assessments tied to process or equipment modifications.
  • Partner cross-functionally with upstream and downstream manufacturing teams, as well as international sites.
  • Contribute to future Drug Product tech transfer activities as new facility capabilities come online.
  • Ensure regulatory and GMP compliance; support health authority inspections.

Skills

Team leadership
MSAT experience
Vaccine/biopharma expertise
Process troubleshooting
Cross-functional collaboration

Education

Bachelor's degree

Tools

UFDF
Chromatography
Bioprocessing equipment

Job description

Barrington James is seeking an MSAT Lead for a global biopharmaceutical manufacturer undergoing site transformation, to lead a 4-6 member MSAT team and contribute as a hands-on technical resource for process troubleshooting and lifecycle management.

You will partner with upstream/downstream teams and international sites, support drug substance and drug product tech transfer as new facilities come online, and ensure GMP compliance and readiness for inspections.

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