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Home / Job / CIPLA Career Opportunities: Formulator Master in Pharmacy Apply Now 

CIPLA Career Opportunities: Formulator Master in Pharmacy Apply Now 

CIPLA Career Opportunities: Formulator Master in Pharmacy Apply Now 

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

  1. Collate and review Pharma literature from USFDA etc. in order to utilize knowledge during product development

  2. 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

  1. Provide indent through supply chain management to procure the Filters, RM and PM required during product development and submission batches

  2. Prepare regulatory submission data by conducting R&D trials and executing regulatory submission batches at the unit for successful filing

  3. Provide deficiency response support by generating data at R&D/Unit required for approval of the product

Education Qualification

Master in Pharmacy (Specialization in Pharmaceutics)

Relevant Work Experience

4 years experience in R&D (Preferably in  Opthalmic products)

    TO APPLY CLICK HERE

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

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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