Sanofi - Urgent Openings for Freshers & Experienced Production Specialist / QMS Specialist / QC Professionals
QC Professional
Duties & Responsibilities
Sampling and testing of Water, Raw materials, Packing materials.
Preparation of SOPs, STPs and Protocols
Participating in OOS & OOT investigation.
To identify, correct and promptly report unsafe conditions, behaviors, or potentially hazardous situations.
General maintenance of Lab equipment.
Ensure labs are clean and safe (in compliance with GMP) and properly stocked.
Performs other additional job-related duties as required.
Performing routine QC testing of in-process and final products in a GMP lab for release.
Qualifications
A minimum of Master’s degree in Science or Pharmacy is required.
A minimum of 0 to 3 years of experience in Pharmaceuticals is required.
QMS Specialist
- Responsible for the Site Document Management (Document Issuance and Archival)
- Review of the cross functional department Document (SOPs/Specifications etc).
- Documents Issuance and Archival through the Document management system tool.
- Issuance of Numbering (Equipment/Instrument/Layouts etc.) and Management of the master lists.
- Participate in the Investigations resulted due to any Deviations.
- Ensuring accuracy of all documentation Issuance/Archival related activities.
- Handling of Change Controls, Deviations, CAPAs.
- Ensure the audit prerequisites are all time ready (Readiness of Inspection file; Inspection kit etc.).
- Ensure about the periodic revision of the documents and follow up with user for its timely revisions and implementation.
Qualification:
- Education level – Graduate/Post Graduate – B.Pharm/M.Pharm/M.Sc.
- Minimum of 2 to 3 years of relevant Experience.
- Pharmaceutical industry experience (QMS Functions) is a plus
Production Specialist - Officer
Duties & Responsibilities
- Responsible for executing Insulin compounding activities.
- Operate the equipment pertaining to compounding activities.
- To support or suggest for continuous improvements pertaining to processes.
- Responsible for project support and validation support such as effective installation,
Qualifications
- Qualification: Minimum of Bachelor’s degree in applied sciences.
- 2- 3 years experience in Sterile injectable compounding
- Pharmaceutical industry experience is required.
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