Home Head/VP/CEO/President/GM Director R&D | Formulation Development | Teva Pharmaceuticals | Ambernath, MH

Director R&D | Formulation Development | Teva Pharmaceuticals | Ambernath, MH


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: Director – R&D – Formulation Development

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

Job Description:

  • Formulation Development Project Management and monitoring key milestones.
  • Guide and Approve Developmental strategies, new product specifications, master formula, development reports, validation protocols, and reports.
  • Supervise and guide formulation scientists on the development projects.
  • Guide, Support, and co-ordinate to the development team and coordination with Tech Transfer group for the smooth transfer of product from lab to manufacturing scale.
  • Technical Support to Regulatory and QA departments for product registrations

  • Conduct project review meetings, intra-department meetings on new projects, meetings with legal and other R&D teams for new development.
  • Collaboration with Biopharmaceutics and BE center for timely and successful completion of BE studies
  • Evolve effective departmental systems for increased productivity, efficiency, cost/time management, motivation, and team spirit.
  • Co-ordination with the various departments and vendors/suppliers.
  • New equipment sourcing, vendor identifications, preparation of techno-commercial comparison, and recommendations.
  • Active support to senior management with respect to new formulation development
  • Implementation of QbD principles at the development and scale upstage.
  • Preparation and monitoring of development budget and forecast Self-training and development training.

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

Experience: 15 Years, Min 5 Years in Leadership, working for Regulated Markets

Salary: Negotiable

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