Regulatory Affairs Associate I

  Regulatory Affairs

Job title: Regulatory Affairs Associate I

Company: Teva Pharma

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 coll

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! Job Description Lifecycle management on specific products for Europe and international market Responsible at all times that regulatory modules under Product Manager responsibility are up to date, in accordance with agreed procedure as applicable Inform, prepare and submit variations either directly to authorities or to Teva’s 3rd party client business (Medis) Follow up on variation submissions, timelines and approvals, in accordance with agreed procedure as applicable Compile answers to any deficiency questions from authorities or clients Ensure outcomes of variations are communicated in timely manner and databases/lists are up to date at all times, in accordance with agreed procedure as applicable Regular status updates to management Goal setting and follow up together with his/her supervisor Professional communications with both internal and external stakeholders Work on other specialised projects as defined by managers of RA Qualifications M Pharm/ MSc: 3+ years of experience in RA B Pharm/BSc: 5+ years of experience in RA Function Regulatory Affairs Sub Function Medical Regulatory Affairs 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: 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.

Expected salary:

Location: Mumbai, Maharashtra

Job date: Fri, 01 Jul 2022 22:38:19 GMT

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