Job Description

Who are we?

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!

Scheduling, preparation, conduct, documentation and follow-up of assigned GMP/GDP audits in accordance with Teva corporate standards Initial assessment of audit deficiencies, corrective and preventive actions, and overall vendor/site compliance status based on regulatory GMP requirements and specific Teva requirements Communication to stakeholders on potential risk and product impact from observations and GMP deficiencies found during your audits Provide support to Teva site with supplier qualification issues and supplier risk assessment based on audit result when required/requested Support notification to management process in case of critical audit findings in collaboration with audit regional lead and audit plan owner Regular participation in GMP trainings (internal/external) Must be able to travel approximately 75% -both domestic and international

Qualifications

• Post Graduate Degree in Any Science Field or Pharma is preferred
• He /She with minimum 10– 15 years of experience required as a Quality Auditor in a regulated pharmaceutical environment (US and EU) with a minimum of 75 audits performed in a Lead Auditor role

• Strong working knowledge of current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements
• Should be form Pharma Industry / MNC is preferred
• This will be majorly with Inhaler, Syringes, Basic technology sterile, OSD and capsule
• Should have good exp in different site

Function

Quality

Sub Function

Supplier Quality

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’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.