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Opportunity for B.Pharm, M.Pharm in Formulation Tech Transfer at Cipla

Opportunity for B.Pharm, M.Pharm in Formulation Tech Transfer at Cipla

Post : Team Member – Formulation Tech Transfer

Job Description
Job Purpose

Execute the Formulation Technology Transfer activities across all Cipla sites & CMO to standardize, strengthen and improve the technology transfer processes and systems in line with regulations

I. Conduct effective transfer of knowledge about the product and process to formulations manufacturing unit with required documentation for successful implementation of new product technology
II. Identify and list requirements and prerequisites (RM, PM, tooling, accessories, machines, etc.) for execution of batches as per monthly rolling plan
III. Participate in execution of placebo, feasibility, assessment, regulatory and amendment batches within defined timeframe
IV. Gather and collate batch, process, in-process, physical, analytical and stability data for dossier compilation
V. Assist in evaluation and extrapolation of acquired batch data during the transfer process, to define control strategy for commercial launch
VI. Extend technical support to implement CIP, AVD and site transfer activities to drive product life cycle management for sustained growth
VII. Participate in Tech Transfer activities at CMO for new products

Candidate Profile
• B.Pharm/ M.Pharm
• Relevant Work Experience : 5-7 years of experience in formulation development and /or manufacturing, having knowledge of regulatory market

Additional Information
Job ID : 41825
Qualification : B.Pharm/ M.Pharm
Location : Goa
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Formulation Tech Transfer
End Date : 20th 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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