Validation Engineer I - Katalyst Healthcares & Life Sciences
Venice, FL 34284
About the Job
Responsibilities and Requirements:
- Note: Need 2-3 managerial references (Name,Title,Email,Contact, Linkedin).
- Please also make sure all resume have graduation dates.
- 5 to 7 years of validation engineering experience with equipment, and / or facilities within a cGMP or FDA regulated environment.
- GMP/cGMP process experience.
- Clear understanding of industry regulated guidelines for the validation of cGMP facilities.
- Relevant experience within the Pharmaceutical, or Biotechnology industries.
- Develop, write installation (IQ), operational (OQ) and performance qualification (PQ) protocols for production equipment, laboratories and process validation for production processes.
- Coordinate execution of validation protocols.
- Analyze validation test data - determine systems or processes have met validation criteria.
- Prepare validation or performance qualification protocols for manufacturing processes, systems, equipment for production.
- Prepare summary reports for the completed qualifications including recommendations.
Source : Katalyst Healthcares & Life Sciences
