Quality Systems Engineer - GMP & Change Control Lead

Teva Pharmaceuticals; Salt Lake City (UT); Sur place; USD 90 000 - 130 000; Plein temps

Résumé du poste

Teva Pharmaceuticals in Salt Lake City, Utah, seeks a Quality Systems Specialist to manage pharmaceutical quality systems, ensure CGMP compliance, and drive change control and document management across the site.

The role emphasizes continuous improvement, participating in inspections, and supporting regulatory compliance with cross-functional collaboration to optimize manufacturing operations.

Qualifications

• Bachelor's degree in a scientific discipline with 7+ years in the industry and 3+ years in Pharmaceutical QA.
• Experience with GMP quality systems and site audits is preferred.
• Strong collaboration with Operations, MLT, R&D and Supply Chain.

Responsabilités

• Overseeing change management activities and maintaining quality records.
• Participating in inspections/audits and supporting regulatory compliance.
• Ensuring CGMP alignment and continuous improvement of QA processes.

Connaissances

Quality management systems

Change control

Document management

Continuous improvement

Regulatory compliance

Formation

Bachelor's degree in science (biology, chemistry or related)

Description du poste

Teva Pharmaceuticals in Salt Lake City, Utah, seeks a Quality Systems Specialist to manage pharmaceutical quality systems, ensure CGMP compliance, and drive change control and document management across the site.

The role emphasizes continuous improvement, participating in inspections, and supporting regulatory compliance with cross-functional collaboration to optimize manufacturing operations.