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Career for Master in Pharmacy as Formulator at Cipla

Career for Master in Pharmacy as Formulator at Cipla

Post : Formulator

Job Description
Job Purpose

Execute end to end formula and process development of  Opthalmic products following good laboratory practices and continuously monitor its data and quality to have robust a product within the budget, timeline and regulatory standards.

Accountabilities
I. Collate and review Pharma literature from USFDA etc. in order to utilize knowledge during product development
II. Provide and submit all stage gates documents to CFT on the basis of data generated from development trials to execute batches at plant
III. Gather data from pre-formulation studies by carrying out characterization of reference product and optimize the formula in order to develop a robust product
IV. Provide indent through supply chain management to procure the Filters, RM and PM required during product development and submission batches
V. Prepare regulatory submission data by conducting R&D trials and executing regulatory submission batches at the unit for successful filing
VI. Provide deficiency response support by generating data at R&D/Unit required for approval of the product

Candidate Profile
Master in Pharmacy (Specialization in Pharmaceutics)
4 years experience in R&D (Preferably in  Opthalmic products)

Additional Information
Experience : 4 years
Qualification : M.Pharm
Location : Vikhroli, Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Formulation R&D
End Date : 30th September, 2020

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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