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Bioprocess Technician
GroupA • Hopewell, NJ 08525 • Posted 2 days ago via LinkedIn
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In-person • Full-time • Contract • Mid Level
Job Highlights
Using AI ⚡ to summarize the original job post
The Bioprocess Technician role involves following cGMP procedures to support manufacturing execution and automated recipes, including Clean-In-Place (CIP) & Steam-In-Place (SIP), media preparation and transfers, filtration, cell culture sampling, monitoring, and transferring, harvest operations, equipment and process troubleshooting, deviation identification and closure, cGMP procedure development and optimization, and equipment validation. This is a contract position with the opportunity to extend or convert to full-time employment based on budget and performance.
Responsibilities
- Follow cGMP procedures to support manufacturing execution and automated recipes
- Clean-In-Place (CIP) & Steam-In-Place (SIP)
- Media preparation & transfers / filtration
- Cell culture sampling, monitoring & transferring
- Harvest operations
- Equipment & process troubleshooting
- Deviation identification, reporting and closure
- cGMP procedure development and optimization
- Cleaning and garbage discharge
- 6S operation
- Equipment validation (bioreactor IOQ and PQ study, but not limited to the other cell culture validation activity)
Qualifications
Required
- At least 3-5 years working in cell culture area in Biopharm industry
- Familiar with single use bioreactor, such as Wave bioreactor, Sartorius or Cytiva bioreactor 200-2000L
- Familiar with inoculation aseptic technique
- Familiar with stainless steel vessel operation with DCS control (Medium Preparation, CIP/SIP)
- Familiar with Part washer or autoclave operation
Full Job Description
This is a contract until 01/31/2025, with the opportunity to extend longer or convert to FTE based on budget/performance.
Benefits: (Medical, Dental, Vision, Life Insurance)
- Follow cGMP procedures to support manufacturing execution and automated recipes
- Clean-In-Place (CIP) & Steam-In-Place (SIP)
- Media preparation & transfers / filtration
- Cell culture sampling, monitoring & transferring
- Harvest operations
- Equipment & process troubleshooting
- Deviation identification, reporting and closure
- cGMP procedure development and optimization
- Cleaning and garbage discharge
- 6S operation
- Equipment validation (bioreactor IOQ and PQ study, but not limited to the other cell culture validation activity).
Requirements
- At least 3-5 years working in cell culture area in Biopharm industry.
- Familiar with single use bioreactor, such as Wave bioreactor, Sartorius or Cytiva bioreactor 200-2000L
- Familiar with inoculation aseptic technique
- Familiar with stainless steel vessel operation with DCS control (Medium Preparation, CIP/SIP)
- Familiar with Part washer or autoclave operation
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