Sr. Compliance Specialist

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, TrackWise, Veeva, and Qdocs. Ability to manage multiple priorities and reporting requirements. Ability to motivate and influence others with and/or without direct supervisory authority. Ability to communicate effectively with excellent written and oral communication skills. Ability to interact positively and collaborate with co‑workers, management and internal/external partners. Detail oriented with ability to analyze information, develop possible solutions, create metrics and articulate the link to business needs/objectives. Project management and advanced presentation skills. Self‑directed with ability to organize and prioritize work. Problem Solving Proactively works on problems of a moderate to complex scope where evaluation of contributing factors requires the analysis of situations or data and an in-depth knowledge and evaluation of various known and unknown factors. Seeks out all resources when selecting methods and techniques for obtaining results. Acts independently and proactively to recommend and administer methods and procedures for problem resolution.

WORKING ENVIRONMENT

Exposure to low noise levels in an office environment. Occasional exposure to moderate to loud noise levels. Occasional exposure to moving mechanical parts or equipment. Required to wear personal protective equipment (PPE) as needed when in production areas (i.e. safety glasses, respirator, hearing protection, gloves, etc.). How We’ll Take Care of You At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one‑stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short‑term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. We offer a competitive benefits package, including Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls. Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan. Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays. Life and Disability Protection: Company paid Life and Disability insurance. Additional benefits include, but are not limited to: Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to View email address on click.appcast.io with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address. EOE including disability/veteran #J-18808-Ljbffr Teva Pharmaceuticals