1+ months

Director Compliance Quality SMSO

Parsippany, NJ 07054

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

The main purpose of your job will be to ensure that a Solids Manufacturing & Supply Operations (SMSO) Quality Compliance System is in place, securing compliance of activities, quality risk management, escalation of risks, and continuous improvement. Your role will include providing governance through strong collaboration with manufacturing site operations to foster excellence in inspection management and inspection readiness at Teva sites. You will support manufactuing site remediatio actvities directly.  You will also interact across the matrixed organization specifically with Teva Global Quality Compliance, Manufacturing Science & Technology, Research & Devleopment, Supply Chain Operations, and other network manufacturing supply sites.

This role will ensure that each site within the SMSO segment receives the right level of support to sustain and continuously improve GMP compliance, to strategize remedial plans, to solve quality-related service issues, to identify areas of improvement for quality operational performance in line with business needs and in accordance to Teva standards. Moreover, you will foster and develop onsite Quality culture across the SMSO segment.


    • Bachelor's Degree* chemistry, microbiology, pharmacy, engineering, or related science-based degree.
    • Master's Degree preferred in science, business, healthcare, or an equivalent combination of education and experience related to Quality Assurance/Quality Control - advantage at large and complex sites
      • Solids Manufacturing / SME experience required*.  Medical Device expertise a plus.
        • Experience*: 20+ years of experience as a functional leader with technical, team management, and operational responsibility. Continuous professional development and industry working group participation a plus.
          • Expert understanding and insight into the different aspects of quality management systems, functions and operations in QC, QA, Compliance, Data Management*.
            • Must be able to travel based on business need; up to 50% when critically required (domestic and international)*



Sub Function

Quality Compliance

Reports To

Senior Director Quality Compliance-Solids Manufacturing Supply Operations

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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. 


Posted: 2021-01-21 Expires: 2021-05-01

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Director Compliance Quality SMSO

Teva Pharmaceuticals
Parsippany, NJ 07054

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