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.

REQUIREMENTS:

》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 ⬇️⬇️

📧pranita.padte@teva.co.in📧

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