Vacancy for Analytical Research Associate, Regulatory Affairs at Medreich

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Medreich is a fully integrated pharmaceutical company with an established presence across the globe. The company is involved in the CMO & CDMO business of pharmaceutical preparations in various dosage forms catering to diverse Therapeutic categories.  Medreich has an advanced state of the art Research and Development centre with proven scientific competence to develop formulations as Patent Non-infringing and Niche generics in differentiated dosage form for global regulated markets.

Department - Analytical Research & Development (AR&D) / Formulation R&D. Qualification : M Pharma (Pharmaceutical Analysis) / M.Sc / PhD Chemistry/Analysis (Only) Required Minimum Experience 1 to 6 Years.
Job Profile :  Candidate should have knowledge in Method development, Method validation of different pharmaceutical dosage forms. Hands on experience/ knowledge in handling Analytical work related to DS and DPs in different phases with a proven track record (having worked with Global partners/ International exposure). Hands on experience in Chromatography (HPLC, UPLC, HSGC), Spectroscopy (FTIR, UV), dissolution apparatus and Particle size measurements. KEY Skills: HPLC Method Validation, UV, Dissolution, Apparatus UPLC Method Development FTIR. & RS.

Qualification : B.Pharm / M.Pharm only

Experience : 1-5 years of ROW/Europe/ ASEAN and AU/NZ market experience.
Required only Male Candidates
Note - candidates should have good communication and interested to work for shifts.

Interested candidates can send their resumes to

Analytical RA :

Regulatory Affairs : /

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