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Pfizer · 1 day ago

Tech Transfer Engineer II

United States - Massachusetts - Andover

Full-time

Hybrid

Entry, Mid Level

$69K/yr - $111K/yr

2+ years exp

Pfizer is a global pharmaceutical company dedicated to advancing health and wellness. The Tech Transfer Engineer II will join the Andover Clinical Manufacturing Facility team, responsible for overseeing tech transfer activities and ensuring the successful production of clinical drug substances. This role involves collaborating with various teams to improve manufacturing processes and support project ownership in a cGMP environment.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine

No H1B

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 development lines to improve scale up processes and identify best TT practices

Partner with 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

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

Qualification

Biologics GMP manufacturingTech TransferBioprocessing techniquesProduction Control SystemsERP SystemsDocument Management SystemsTeam collaborationCommunication skillsWork independently

Required

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

Preferred

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), ERP Systems (i.e. Microsoft Dynamics and/or SAP) and other business systems (Document Management Systems, LIMS, Microsoft Word, Excel, etc.)

Ability to execute against SOPs and document entries in a compliant manner

Demonstrated capability to work as a team member in a matrix manufacturing team

Excellent oral and written communication skills

Ability to work under minimal supervision