Now Hiring: Stability & Validation Supervisor
Specified Purpose Contract | Pharmaceutical Industry | On-Site
We’re looking for a motivated Stability/Validation Supervisor on a specified purpose contract. Reporting to the QC Manager, you’ll lead a dynamic team, managing all aspects of stability programs and validation activities — from scheduling batches to ensuring full regulatory compliance.
Key Responsibilities:
Oversee stability and validation programs (Process, Analytical, Cleaning)
Lead and develop a high-performing lab team
Ensure all protocols, reports, and documentation are audit-ready
Collaborate across departments to hit key site targets
Act as SME during audits and tours
What You’ll Need:
Degree in Chemistry, Analytical Science, Pharma or Forensic Science
Strong IT & documentation skills
Eye for detail and a proactive approach
Excellent communication and leadership qualities
Be part of a collaborative and quality-focused team driving innovation and compliance.
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