Teva Pharma Walk-in interview @ Ambernath | Multiple Opening for ADL, F&D, Analytical Research, Formulation Research etc.| 21 December 2022

Job location: Ambernath

Join us and be a part of this learning, Progress and growth journey at TEVA !, if new challenges and a dynamic environment interest you.


Scientific Publisher Associate/ Scientific Publisher/ Principal Scientific Publisher- ADL & F&D

  • Preparatio of documents and facilitation of Documentation management in R&D.
  • Preparation of documents based on the scientific input from the Analytical and F&D team.
  • Preparation of high impact presentations including graphs, Charts and statically analysis of Data.
  • Continuously improve of documentation system to increase efficiency and compliance with cGMP or other Regulatory requirements.
  • Excellent in Oral and written Communication.

Qualification and Experience:

Bachelor’s/Master’s degree in a scientific discipline with minimum 5 to 12 years of experience. Candidates currently having experience in ADL and F&D are also preferred.

Analytical Research I/II/III-Nitrosamine

  • To execure the Aitrosamines Analytical activities in an effective manner based on the givers timelines to facilitate the progress of the ANDA projects.
  • To give the Analytical support to Formulation Development and Process/Products Validation activities.
  • To perform the Analytical Method Development, Method validation and Method transfer, Batch analysis activities for development project.

Qualification and Experience:

M.Sc Chemistry with minimum 1 to 8 years of Experience. Candidates should have experience in handling of LCMS/MS and GCMS/MS like instruments.

Analytical Research I/II/III

  • Finished Product testing like Analytical Development and Analytical Method Validation by HPLC, GC, IC, UV etc.
  • Development of Analytical Methods, Analytical Method validation and transfer and Analytical of finished product R&D samples.

Qualification And Experience:

M.Sc, M.Pharm, Ph.D with minimum experience 4 to 12 years.

Formulation Research II/III

  • Pharmaceutical dosage form development experience-All types of solid-Oral Dosage forms.
  • Thorough knowledge of cGMP & ICH guidelines and QbD Principles, Exposure to scale-up of project for technology transfer plant.

Qualification and Experience:

M.Pharm/ PhD with experience having 3 to 10 years.

Walk-in Date: 21st December 2022 (Wednesday)

Time: 10 am to 4 pm

Venue: Watson Pharma Pvt.Ltd. (A Teva co.) Unit-II, Plot No.K7, Additional MIDC, Ambernath East, 421506

Interested candidates may also share their resume to ⬇️⬇️


Please note: Candidates must carry their valid identity proof updated resume, highest qualification certificate, latest increment letter pay slips of the last 3 months

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