Description

Job DescriptionGreat development opportunity to work as a Senior Quality Control Specialist with a global, research-driven pharmaceutical manufacturer focused on developing innovative treatments for diseases and conditions with limited or no satisfactory treatment options currently available. This is an excellent opportunity to gain hands-on experience supporting cutting-edge therapies while contributing to meaningful patient outcomes.

Senior Quality Control Specialist

Location: Gainesville

Contract: 2-Year Contract | Full-Time | On-Site | 8:00 AM–4:30 PM

Benefits: Medical, Dental, Holiday, PTO 401K matching

The Senior Quality Control Specialist supports QC operations through documentation management, data integrity support, laboratory record maintenance, and compliance activities within a GMP-regulated environment. This role assists with controlled documentation, sample tracking, reagent ordering, LIMS reporting, and SAP record management while ensuring compliance with quality standards and internal procedures.

• Distribute and reconcile QC documentation
• Prepare and review 2008 forms and related records
• Maintain QC file room and document archives
• Support sample receipt, LIMS reporting, and serial file compilation
• Order and track laboratory reagents and supplies
• Utilize SAP and electronic systems for record keeping
• Ensure compliance with GMP and data integrity requirements
• Communicate effectively with laboratory and quality teams
  
  

Qualifications

• Associate’s degree with 2–3 years of related experience OR Bachelor’s degree with 1–2 years of related experience
• Experience in QC, laboratory support, or data management preferred
• Familiarity with LIMS, SAP, and GMP documentation practices
• Strong organizational and communication skills This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
  
  

INDB