MEDVACON
Aseptic Process Development - CDMO
Indianaplos, IN, United States · Full-time
Sponsorship not specifiedDetected 1293 days ago
Customer SupportGMPMolecular BiologyCell CultureLeadershipCollaboration
About the role
- MEDVACON Life Sciences works with many leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.
- Our focus is cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.
- Our leading CDMO client is eager to hire an Aseptic Downstream Process Development SME for their Indianapolis site.
Requirements
- Provide technical expertise and leadership in science & technology and requires close collaboration with internal stakeholders.
- Bachelors Degree
- 5+ years exp in a cGMP pharma/biotech setting
- Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing Organizations
- Experience with cell culture technologies, molecular biology, and aseptic processing
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