Sr. Compliance Specialist

Location: Salt

We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact This position will be responsible for Quality Compliance Oversight, Quality Council Management Review, Site Compliance Metrics, Knowledge Management, Site Inspection Readiness program, Internal Audit program, Partner Management activities, and Supplier Qualification and Vendor Management program. The position is responsible for the development and monitoring of corrective action plans related to trends identified from inspection and audit observations.

Location:

SLC West
4710 Wiley Post Way, Salt Lake City, UT 84116

How You’ll Spend Your Day All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.

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.

Maintain work areas and perform duties safely and efficiently in accordance with company policies, cGMPs, SOPs, and Batch Records.

Responsible for performing additional related duties as assigned.

Your Skills and Experience Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

Education/Certification/

Experience:

Bachelor’s Degree, preferably in a scientific or engineering discipline, or equivalent education/experience with a minimum of 7 years relevant progressive experience in the pharmaceutical or related industry.

Strongly prefer a minimum of 3 years performing audits and measurements of GMP Quality Systems, preferably in the pharmaceutical industry.

Requires experience and knowledge of cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.

Working knowledge of FDA, EMA, DEA, EPA and other regulatory requirements for a research and commercial environment.

Experience providing support for regulatory agency inspections preferred.

Experience with writing and negotiating Quality Technical Agreements preferred.

Experience in a pharmaceutical manufacturing environment preferred.

Experience with internal/external auditing is preferred.

ASQ CQE/CQA Certification (or equivalent) is preferred.

Also Good to Have Skills/Knowledge/Abilities:

Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Track Wise, Veeva, and Qdocs.

Ability to manage multiple priorities and…