Group Leader Regulatory Affairs

☞ Teva Pharmaceuticals

看过: 101

更新日: 06-05-2024

位置: Navi Mumbai Maharashtra

类别: 药剂师/药剂师代表 列印

行业: Pharmaceutical Biotechnology

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工作内容

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

  • Provide routine publishing support to Global Regulatory Activity.
  • Scheduling & Managing the daily activities and workload of site publishing team.
  • Ensuring that individuals are trained and comply with all SOPs and internal publishing standards.
  • Coordinate and lead major/complex and routine/lifecycle management eCTD submission projects.
  • Prepare and deliver performance management and career development plans for team & provide regular feedback of the team to the reporting manager.
  • Perform performance management activities including goal-setting, development plans and annual appraisals for the team after liaising with the manager.
  • Participate in cross-site project teams working on initiatives as defined by the RSM Senior Leadership.
  • Demonstrated skill in working collaboratively in a fast-paced, time-sensitive environment with ability to meet critical deadlines.

Qualifications

Qualifications:

  • Bachelor’s/Master’s degree in Pharmacy or Masters in Science required

Experience

  • Total years of experience required for the role: 8+ years
  • Relevant years of experience: 7+ years (core Publishing)
  • Experience of leading a team: Preferred

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: 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.
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最后期限: 20-06-2024

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