Sr. Compliance Specialist
Teva Pharmaceuticals
August 20, 2026
Remote friendly (Salt Lake City, UT)
United States
Corporate Functions
Responsibilities:
- Prepare and support communication of site quality system status through management review forums.
- Manage Quality Technical Agreements (QTA) with internal and external partners to ensure compliance.
- Lead and execute internal audits to verify adherence to pharmaceutical manufacturing regulations.
- Coordinate and manage external audits/inspections, including timely responses and CAPA tracking.
- Oversee Inspection Readiness program to maintain site preparedness.
- Collaborate with Site Operations and Quality Management to resolve compliance issues promptly.
- Conduct Knowledge Management activities, including regulatory review and gap assessments.
- Support investigation reviews and corrective action plans, ensuring proper documentation and notification.
- Manage vendor/supplier qualification and related compliance activities.
- Ensure periodic document reviews and gap assessments for department and site compliance.
- Own and update procedures for assigned responsibilities.
- Lead special cross-functional projects and present findings to senior management.
- Complete required training and maintain compliance with all assignments.
- Perform duties safely and efficiently in accordance with policies, cGMPs, SOPs, and Batch Records.
Qualifications:
- Bachelor’s degree (preferably scientific/engineering) or equivalent; minimum 7 years relevant progressive experience in pharmaceutical or related industry.
- Strongly prefer 3 years performing audits and measurements of GMP Quality Systems.
- Knowledge of cGMP and applicable regulatory requirements for pharmaceutical products/quality systems.
- Working knowledge of FDA, EMA, DEA, EPA and other regulatory requirements.
- Preferred: support for regulatory agency inspections; writing/negotiating QTA; pharmaceutical manufacturing environment; internal/external auditing.
- Preferred: ASQ CQE/CQA (or equivalent).
Application instructions:
- Apply through the internal career site on Twist.
- Prepare and support communication of site quality system status through management review forums.
- Manage Quality Technical Agreements (QTA) with internal and external partners to ensure compliance.
- Lead and execute internal audits to verify adherence to pharmaceutical manufacturing regulations.
- Coordinate and manage external audits/inspections, including timely responses and CAPA tracking.
- Oversee Inspection Readiness program to maintain site preparedness.
- Collaborate with Site Operations and Quality Management to resolve compliance issues promptly.
- Conduct Knowledge Management activities, including regulatory review and gap assessments.
- Support investigation reviews and corrective action plans, ensuring proper documentation and notification.
- Manage vendor/supplier qualification and related compliance activities.
- Ensure periodic document reviews and gap assessments for department and site compliance.
- Own and update procedures for assigned responsibilities.
- Lead special cross-functional projects and present findings to senior management.
- Complete required training and maintain compliance with all assignments.
- Perform duties safely and efficiently in accordance with policies, cGMPs, SOPs, and Batch Records.
Qualifications:
- Bachelor’s degree (preferably scientific/engineering) or equivalent; minimum 7 years relevant progressive experience in pharmaceutical or related industry.
- Strongly prefer 3 years performing audits and measurements of GMP Quality Systems.
- Knowledge of cGMP and applicable regulatory requirements for pharmaceutical products/quality systems.
- Working knowledge of FDA, EMA, DEA, EPA and other regulatory requirements.
- Preferred: support for regulatory agency inspections; writing/negotiating QTA; pharmaceutical manufacturing environment; internal/external auditing.
- Preferred: ASQ CQE/CQA (or equivalent).
Application instructions:
- Apply through the internal career site on Twist.