Onsite Senior CQV Engineer Peptide Manufacturing; GMP
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Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Manufacturing Engineer
Job Description & How to Apply Below
i-Pharm GxP in Lebanon, Indiana is seeking a Senior CQV Engineer to join a major peptide API manufacturing capital program. The role is hands-on, field-based, and requires strong experience delivering commissioning, qualification and validation from construction through handover.
Responsibilities include IQ/OQ/PQ protocol development, P&, and collaboration with cross-functional teams to ensure GMP-compliant systems. 12-month contract with full onsite work five days a week.
For the Onsite Senior CQV Engineer for Peptide Manufacturing (GMP) position at i-Pharm GxP, we are reviewing applications now.
The Onsite Senior CQV Engineer for Peptide Manufacturing (GMP) position in the Engineering field is open for applications.
We have an opening for a Onsite Senior CQV Engineer for Peptide Manufacturing (GMP) in IN, United States within Engineering.
This role, Onsite Senior CQV Engineer for Peptide Manufacturing (GMP) at i-Pharm GxP, could be your next opportunity.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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