Compliance Specialist III
Teva Pharmaceuticals
August 25, 2026
On-site
Salt Lake City, UT
Corporate Functions
Responsibilities:
- Oversee Quality Compliance, Quality Council Management Review, Site Compliance Metrics, Knowledge Management, Inspection Readiness, Internal Audit, Partner Management, and Supplier Qualification/Vendor Management.
- Develop/monitor CAPAs for trends from inspection and audit observations.
- Prepare management review communications on site quality system status.
- Manage Quality Technical Agreements (QTAs) with internal/external partners.
- Lead internal audits; coordinate external audits/inspections with timely responses and CAPA tracking.
- Conduct knowledge management (regulatory review and gap assessments); support investigation reviews and corrective action documentation.
- Perform periodic document reviews/gap assessments; own/update assigned procedures.
- Lead cross-functional projects and present findings to senior management.
- Complete required training; perform duties per company policies, cGMPs, SOPs, and Batch Records.
Qualifications:
- Bachelor’s degree (scientific/engineering preferred) or equivalent with 7+ years progressive pharmaceutical/related industry experience.
- Prefer 3+ years auditing/measuring GMP Quality Systems.
- Requires cGMP and regulatory knowledge (FDA/EMA/DEA/EPA and others).
- Prefer regulatory agency inspection support; QTA writing/negotiation; pharmaceutical manufacturing environment; internal/external auditing; ASQ CQE/CQA (or equivalent).
Skills (preferred):
- MS Office, LMS, ERP (SAP/Oracle), quality/manufacturing systems (LIMS, TrackWise, Veeva, Qdocs); manage priorities; influence; strong written/oral communication; analytical/metrics; project management.
Benefits (explicitly stated):
- Health, 401(k) with match, paid time off, life/disability, and additional listed benefits.
Application instructions:
- Apply via internal career site on Twist.
- Oversee Quality Compliance, Quality Council Management Review, Site Compliance Metrics, Knowledge Management, Inspection Readiness, Internal Audit, Partner Management, and Supplier Qualification/Vendor Management.
- Develop/monitor CAPAs for trends from inspection and audit observations.
- Prepare management review communications on site quality system status.
- Manage Quality Technical Agreements (QTAs) with internal/external partners.
- Lead internal audits; coordinate external audits/inspections with timely responses and CAPA tracking.
- Conduct knowledge management (regulatory review and gap assessments); support investigation reviews and corrective action documentation.
- Perform periodic document reviews/gap assessments; own/update assigned procedures.
- Lead cross-functional projects and present findings to senior management.
- Complete required training; perform duties per company policies, cGMPs, SOPs, and Batch Records.
Qualifications:
- Bachelor’s degree (scientific/engineering preferred) or equivalent with 7+ years progressive pharmaceutical/related industry experience.
- Prefer 3+ years auditing/measuring GMP Quality Systems.
- Requires cGMP and regulatory knowledge (FDA/EMA/DEA/EPA and others).
- Prefer regulatory agency inspection support; QTA writing/negotiation; pharmaceutical manufacturing environment; internal/external auditing; ASQ CQE/CQA (or equivalent).
Skills (preferred):
- MS Office, LMS, ERP (SAP/Oracle), quality/manufacturing systems (LIMS, TrackWise, Veeva, Qdocs); manage priorities; influence; strong written/oral communication; analytical/metrics; project management.
Benefits (explicitly stated):
- Health, 401(k) with match, paid time off, life/disability, and additional listed benefits.
Application instructions:
- Apply via internal career site on Twist.