Tech Transfer Engineer II

Pfizer • Andover, MA

6h • $68,600 - $114,300 • Hybrid

About The Position

The Tech Transfer Engineer II will be joining the Pfizer Andover Clinical Manufacturing Facility (ACMF) team. The ACMF is a facility located on the Pfizer Andover, MA campus and is responsible for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio. The ACMF resides within the Research and Development organization. The ACMF Technology Transfer Team is responsible for incoming product site assessment, preparatory activities, campaign readiness, and overall product/project ownership to support ACMF manufacturing of clinical drug substance.

Requirements

• BS/BA in Chemical Engineering, Biotechnology, Microbiology, Cell Biology, Biochemistry or equivalent +2 years of experience, or MS + 0 years of experience.
• Previous experience in Biologics GMP manufacturing and/or Biologics Tech Transfer
• Ability to execute against SOPs and document entries in a compliant manner
• Demonstrated capability to work as a team member in a matrix team
• Excellent oral and written communication skills
• Must have permanent work authorization in the United States.

Nice To Haves

• Experience with Tech Transfer, facility fit assessments, and engineering design
• Knowledge of bioprocessing techniques and equipment
• Experience in a GMP manufacturing role
• Experience with Production Control Systems (i.e. DeltaV), electronic batch records (i.e. Master Control), and other electronic business systems (Document Management Systems, Quality Management Systems, LIMS, Microsoft Word, Excel, etc.)

Responsibilities

• Serve as tech transfer lead for incoming projects on a rotating basis (approximately 1-2 per year)
• When not serving as TT lead, execute tech transfer activities in support of all ACMF campaigns
• Work with BRD development lines to improve scale up processes and identify best TT practices
• Partner with BRD development lines on complex technical initiatives
• Lead/support the creation of manufacturing batch records and other GMP documentation
• Execute and troubleshoot upstream and downstream processes in a cGMP environment
• Advocate for and implement technology, digital, and continuous improvement strategies
• Authorship of SOPs for upstream and downstream unit operations
• Data analysis and communication/collaboration with tech transfer team, production operations, development labs, and quality
• Support implementation of new technologies and equipment
• Support investigations as needed
• Support facility audits as needed

Benefits

• 401(k) plan with Pfizer Matching Contributions
• Additional Pfizer Retirement Savings Contribution
• Paid vacation, holiday and personal days
• Paid caregiver/parental and medical leave
• Health benefits to include medical, prescription drug, dental and vision coverage
• Relocation assistance may be available based on business needs and/or eligibility

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level