MEDVACON
GMP Quality Validation - Lab
Kansas City, MO, United States · Contract
No sponsorshipDetected 1345 days ago
RecruitingGMPFDA Regulatory
About the role
- MEDVACON Life Sciences works with leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.
- Our focus is providing consulting and talent acquisition services for cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.
- Validation representative for laboratory validation activities, including Equipment Qualification and systems administration.
Requirements
- 1 YEAR WITH OPTION TO EXTEND
- Bachelors in related Field or 2-10 years of Scientific or Engineering experience
- 3+ years work exp in project/process engineering and validation of FDA-covered processes, as well as QA experience in a pharmaceutical environment.
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This listing is sourced directly from MEDVACON's careers page and normalized into a canonical job model.