QC / Validation Specialist

QC / Validation Specialist | Hybrid

A Colorado manufacturer moving into API manufacturing is looking for a QC / Validation Specialist.

This hands-on role will get lab procedures, controls and validation records ready for pharma GMP.

It starts part-time with the potential to convert to a permanent role, and it’s onsite or hybrid in Northern Colorado.

You should apply if you have:

• QC experience in a GMP-regulated API or pharmaceutical manufacturing environment
• Knowledge of analytical methods, specifications and laboratory controls
• Equipment qualification and method validation or transfer experience
• Familiarity with data integrity and laboratory investigations
• Strong GMP documentation skills