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Bioprocess Specialist 2 - CONTRACT

Genefab
Alameda, CAonsite$40 - $50Feb 18, 2026·Posted 1 month ago
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Domain

Must-Have Requirements

  • High school diploma or equivalent
  • 3-4 years biotech or pharmaceutical manufacturing experience
  • Proficiency in cGMP cleanrooms and aseptic techniques
  • Advanced understanding of pipetting and micro pipetting
  • Familiarity with cGMP standards and Good Documentation Practices
  • Ability to stand for extended periods
  • Ability to lift up to 20 pounds
  • Strong communication and teamwork skills

Nice to Have

  • -Associates or higher degree in Biology, Life Science, or Engineering
  • -Demonstrated ability to identify and implement improvements to work procedures

Description

The Bioprocess Specialist II plays a critical role in the cell and gene therapy manufacturing processes at GeneFab. This position involves executing both upstream and downstream processes in a GMP-compliant cleanroom environment, with responsibility for troubleshooting, deviation management, training, and contributing to 5S and other improvement initiatives with the goal of ensuring on time delivery and right first-time execution of Manufacturing batches. You will collaborate with Operations, MSAT, Quality, and Facilities teams to ensure consistent production outcomes.

Responsibilities

Technical proficiency in aseptic techniques working with manufacturing equipment/instruments in open and closed systems Organize, coordinate, and lead production activities and ensure execution of processes in production while strictly adhering to cGMP standards Accurately complete batch records, forms, and documentation in line with Good Documentation Practices (GDP). Work as part of a team to support the execution of daily GMP manufacturing activities. Train staff in processing methods, aseptic technique, and cGMP clean room operations. Review batch production records for completeness, accuracy, and to ensure cGMPs and Good Documentation Practices. Initiate and support the closure of Deviation Reports and CAPAs Other duties as assigned by management.

Qualifications

Minimum High School diploma or equivalent experience is required. Associates or higher degree in Biology, Life Science, or Engineering is preferred. 3-4 minimum years of experience in biotech or pharmaceutical manufacturing, preferably in a cleanroom environment. Familiarity with cGMP standards and basic understanding of Good Documentation Practices. Proficiency working in cGMP cleanrooms and aseptic techniques Advanced understanding of pipetting and micro pipetting. Demonstrated ability to identify, challenge, and implement potential improvements to work procedures. Ability to work flexible hours, including nights and weekends, as schedules may shift in this start-up environment. Ability to stand for extended periods and lift up to 20 pounds. Strong communication and teamwork skills, with a willingness to learn.

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