Job Description:
- Pay: $28.00- 31.78/hr to start.
- 1 year contract with the possibility of extension or conversion based on budget and performance.
- Monday- Friday, standard day shift, onsite position.
- Position will mainly be responsible for executing cGMP manufacturing processes, following batch records and SOPs, performing raw material weighing, chromatography, ultrafiltration/diafiltration, and viral vector manufacturing operations using aseptic technique and proper cleanroom practices.
- Responsibilities also include operating single-use systems and MES/EBS transactions, supporting buffer preparation, filter integrity testing, viral vector filling, equipment troubleshooting, and reviewing in-process GMP documentation for accuracy and compliance.
- Position will also be responsible for collaborating with MSAT, Facilities & Engineering, and Quality teams, supporting SOP and MPR revisions, escalating process or equipment issues, and maintaining a safety-first, right-the-first-time manufacturing environment.
- High school Diploma, GED, Associates, or Bachelors degree is required.
- Experience in GMP/ISO regulations is required.
- Experience with downstream purification techniques is required.
- Experience with SOP adherence is required.
- Experience with chromatography is required.
If you are interested in hearing more about the position, please respond to this post with your resume attached
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