- Job title: Bioprocessing Manufacturing Technician
Responsibilities:
- Execute all Upstream Clinical Manufacturing and Development operations, including but not limited to work functions in: cell culture, cell banking, media optimization, seed train preparation, bioreactor operations, harvest/clarification, and technology transfer to manufacturing.
- Execute Manufacturing Batch Records MBR for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulations.
- Activities include maintaining cell culture in various cell culture vessels; preparation of inoculum for bioreactor production and operation of various bioreactors
- Department responsibilities also include assistance with some cell culture process development activities consisting of, cell line characterization, media formulation evaluation, and inoculum process.
Specific Duties:
- Maintain laboratory inventory and equipment.
- Record process development activities and results in appropriate notebooks and spreadsheets.
- Assist in writing standard operating procedures SOPs , specifications, and manufacturing batch records MBRs.
- Participate in cell culture operations according to MBRs in compliance with cGMP regulations and guidelines.
- Participate in the thawing and freezing of cell banks.
- Maintain accurate and current documentation per GBI SOPs.
- Assist with the creation and revision of procedures and material specifications.
- Prepare medium and buffers to support USP projects.
- Maintain the GMP manufacturing areas per GBI SOPs.
- Assist with the execution of bioreactor operations including assembly, sterilization, setup, inoculation, daily checks, maintenance, harvesting, system shutdown and cleaning.
- Possess a thorough knowledge of all company SOPs relating to cell culture and bioreactor operations.
- Recording of counts and equipment used.
- Adhere to all GBI policies and safety guidelines.
- Perform all other duties as assigned.
Requirements:
- BS degree in Science or Engineering, or other related field.
- 1-2 years of experience in a GMP work environment, preferably in Upstream Manufacturing.
You should know: Your safety matters! Vaccination against COVID-19 may be a requirement for this job in compliance with current client and governmental policies. A Kelly recruiter will confirm and share more details with you during the interview process.
Why Kelly®?
Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.
About Kelly®
At Kelly, we’re always thinking about what’s next and advising job seekers on new ways of working to reach their full potential. In fact, we’re a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.
Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.
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