QC 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!