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5 дней назад

Tech Transfer Engineer I (Biologics)

60 200 - 100 400$
Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Релокация
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Tech Transfer Engineer I (Biologics): Executing technology transfer activities and supporting cGMP production of clinical drug substance at Pfizer’s Andover Clinical Manufacturing Facility with an accent on scale-up, GMP documentation, and upstream and downstream process troubleshooting. Focus on creating batch records, implementing new technologies and equipment, analyzing process data, and supporting investigations and facility audits.

Location: United States — Massachusetts — Andover; hybrid work location. Ability to work in a clean room environment is required on a non-routine basis. Permanent U.S. work authorization is required, and U.S. work visa sponsorship is not available. Relocation assistance may be available based on business needs and eligibility.

Salary: $60,200–$100,400 annual base salary, plus eligibility for a 7.5% bonus target.

Company

hirify.global develops and manufactures medicines, including clinical drug substance for its biotherapeutics portfolio.

What you will do

  • Execute technology transfer activities supporting clinical manufacturing campaigns.
  • Work with development lines and Operations on scale-up processes, technical initiatives, and transfer best practices.
  • Lead or support the creation of manufacturing batch records and other GMP documentation.
  • Troubleshoot upstream and downstream processes in a cGMP environment.
  • Implement technology, digital, continuous improvement, new technology, and equipment initiatives.
  • Analyze data, collaborate with development, operations, quality, and technology transfer teams, and support investigations and facility audits.

Requirements

  • Bachelor’s degree in Chemical Engineering, Biotechnology, Microbiology, Cell Biology, Biochemistry, or an equivalent field.
  • Previous professional experience is not required.
  • Authorization to work permanently in the United States for any employer is required.
  • U.S. work visa sponsorship is not available now or in the future.
  • Ability to work in a clean room environment on a non-routine basis.

Nice to have

  • Experience in biologics GMP manufacturing or biologics technology transfer.
  • Knowledge of bioprocessing techniques and equipment.
  • Experience with DeltaV, electronic batch records, document management systems, quality management systems, LIMS, Word, or Excel.
  • Ability to follow SOPs, maintain compliant documentation, and work effectively in a matrix team.
  • Strong oral and written communication skills.

Culture & Benefits

  • Hybrid work arrangement within the Andover clinical manufacturing facility.
  • 401(k) plan with matching contributions and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.

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