HomeHead/VP/CEO/President/GMAssociate Director FRD | Teva Pharmaceuticals | Ambernath, Maharashtra

Associate Director FRD | Teva Pharmaceuticals | Ambernath, Maharashtra


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.

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   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!

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity is 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.


Position: Associate Director – FRD

Location: Ambernath, Thane (MMRDA), Maharashtra, India

Job Description:

  • Supervise and guide the team on development activities as per SOP.
  • Monitoring Key milestones of products under development.
  • Review of Developmental strategies & Patent summary prepared by subordinates.
  • Coordination with inter and intra departments, planning & execution of the development activities as per regulatory requirement.
  • To monitor & ensure timely preparation and approval of various documents pertaining to the Formulation research development department.
  • Review and approval of tentative specifications for Raw material/ Packing material/ finished product.
  • Review and approval of MMF.
  • Coordination and supervision of bio batches manufacturing.
  • Review and approval of Developmental reports and data for dossier.
  • Training & development of self and subordinates.
  • Implementation of QbD principles at development and scale up stage.

Qualification: Ph.D.(Preferable)/ M.Pharma

Experience: Min. 13 Years

Salary: Negotiable

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