Quality Assurance Support Consultant
About the role
ProPharma has improved the health and wellness of patients for the past 25 years by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
This is a 12-month contract (multiple roles), beginning in Q4 2026 through the end of Q3 2027 in Indiana. The QA for QC Representatives will focus on approval of lab associated methods.
Responsibilities
The QA for QC representatives will go through training with the QA team and be responsible for:
- Completion of training on time
- Review of methods
- Approval of methods
- Ensuring communication when barriers arise
Requirements
- Background in Quality Control Laboratories, method review, method approval and method transfer/validation
- 7+ years of relevant experience
- Excellent communication and time management skills to ensure timely reviews and approvals
- LabVantage experience is a plus
- Position is on-site in Indiana
Schedule
This is a 12-month contract (multiple roles), beginning in Q4 2026 through the end of Q3 2027.