Quality Assurance Specialist
Piper Companies · Ridgefield, NJ · 1 mo ago
On-siteQuality AssuranceFull-time
Responsibilities
- Review commercial electronic batch records and documentation for completeness and accuracy in preparation for batch release
- Correct and revise documentation as needed
- Advises manufacturing personnel on proper documentation
- Utilizes knowledge of FDA and GMP regulations to ensure compliance
- Conducts deviation/OOS investigations
Qualifications
- A minimum of 1-5 years’ experience within Pharmaceutical Manufacturing (sterile injectable is preferred)
- Hands-on experience with Batch Record review
- Proficiency in Microsoft Office
- Bachelor’s degree in business or scientific field preferred
Pay
Salary Range is dependent upon experience.
Benefits
Comprehensive benefits package