What are the responsibilities and job description for the QC Supervisor position at EPM Scientific?
Quality Control Supervisor
Location: Danbury, CT
Our client, a leading biopharmaceutical company, is seeking an experienced Quality Control Supervisor to join their team. This role is responsible for overseeing QC operations in a GMP-regulated environment, ensuring compliance with regulatory standards and internal procedures.
Key Responsibilities:
- Supervise and mentor QC analysts; provide technical guidance and support.
- Ensure compliance with cGMP, USP, and 21 CFR Parts 210 & 211.
- Review and approve analytical data, investigations, and CAPAs.
- Troubleshoot analytical instruments (HPLC, GC, PSD) and support method validation and transfers.
- Manage testing schedules for raw materials, finished products, stability, and validation samples.
Qualifications:
- BS in a scientific discipline with 5 years of experience or MS with 3 years.
- Hands-on experience with HPLC and Empower software.
- Strong knowledge of cGMP, USP, and ICH guidelines.
- Supervisory experience required.
This is an excellent opportunity to join a growing organization and make an impact, please apply in directly for more information!