Emcure Pharmaceuticals Released Job Openings On 07/03/2022.Emcure Pharmaceuticals is a fast growing fully integrated Indian pharmaceutical company with global presence engaged in developing, manufacturing and marketing a broad range of pharmaceutical products globally. Our core strength lies in developing and manufacturing differentiated pharmaceutical products in-house, which we commercialize through our marketing infrastructure across geographies and relationships with multi-national pharmaceutical companies.
Vacancy Details:
Emcure Pharmaceuticals Limited Recruiting B.Sc / M.Sc / B.Phrama Candidates with 02-05+Years Experience for Officer  Position.Complete Details for the Officer as follows.
Important Details :
- Location : Pune
- Department:- QA (R&D)/ QA Analytical R&D
- No of Vacancies:01
- Details of Salary:NA
- Opening date for online Application: 07/03/2022
- Mode of application :Online
- How To Apply: Interested can share cv @manojt.kumar@emcure.co.in
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Job Description/Skills Required
· Revision in Method of analysis (MOA) and specification due to Pharmacopoeia updates requiring method development / method changes, if any.
· Receipt of Technical Report, Inter office note, SOP’s, Drug substance specification, Drug product specification, Raw material specification, In-process specification and Method of Analysis.
· Initiation and Handling of change controls related to preparation / revision in specification, Method of Analysis, Standard test procedure, Standard operating procedure and related documents.
· Updation, revision and loading of specification in SAP system.
· Review of SAP generated specification.
· Preparation / revision and review of Drug substance specification, Drug product specification, Raw material specification, In-process specification, Method of Analysis, Standard test procedure and Standard operating procedure as per the requirement.
· Initiation of change control for change in SAP specification.
· Concurrence/ review of change implementation of change control forms as a designee of Department Head/Site QA.
· Issuance of documents to relevant sites (i.e. Specifications, MOA’s, STP’s and SOP’s).
· Initiation and review of Deviation, Discrepancy and Risk assessment reports.
· To ensure compliance to Ethical conduct and data integrity policy.
· Perform additional tasks as assigned by Team leader and Head of department to enhance quality system management, cGMP & compliance.
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