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Tech Transfer Engineer II

Job in Andover, Essex County, Massachusetts, 05544, USA
Listing for: Rangam
Full Time position
Listed on 2026-01-29
Job specializations:
  • Pharmaceutical
    Validation Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 68600 USD Yearly USD 68600.00 YEAR
Job Description & How to Apply Below

Rangam is seeking candidates for a Direct Hire role as a Tech Transfer Engineer II with our client, one of the world’s largest pharmaceutical companies.

Seeking candidates in Andover, MA or willing to relocate.

This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week or more as needed.

Why Patients Need You

Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in client s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.

What

You Will Achieve

The Tech Transfer Engineer II will be joining the client s Andover Clinical Manufacturing Facility (ACMF) team. The ACMF is a facility located on the client s Andover, MA campus and is responsible for cGMP production of phase I/II clinical drug substance supporting the client s Biotherapeutics portfolio. The ACMF resides within the Research and Development organization. The ACMF Tech 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.

How

You Will Achieve
  • 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
Qualifications

Must-Have

  • 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

Nice-to-Have

  • 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. Delta

    V), 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
PHYSICAL/MENTAL REQUIREMENTS

Ability to work in a clean room environment (non-routine)

Work Location Assignment:
Hybrid.
This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week or more as needed.

The annual base salary for this position ranges from $68,600.00 to $. In addition, this position is eligible for participation in client s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with client s Matching Contributions and an additional client s Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.

Learn more at client s Candidate Site – U.S. Benefits | (us candidates.my**). Compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

To find out more about Rangam, and this role, click the apply button.

Satnam Singh

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