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Mylan Laboratories was founded in West Virginia in 1961, Mylan is a Global Pharmaceutical company making High-Quality Medicines and a Big Generic Player.
Mylan considers its Global workforce as its Biggest & Most Valuable Asset. Each member of its Team is a passionate supporter of its cause to deliver better health for a better world
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Unconventional. Relentless. Committed. Passionate.
These are some of the traits of the people of Mylan – people who know it’s not about them but, instead, about the 7 billion people relying on them to provide access to quality medicine and to set new standards in healthcare. People who know that, together, we can change the world, 7 billion people, one person at a time.
This is how we’re creating better health for a better world.
Changing the world for the better takes skill, passion, drive, and you.
If you have what it takes to help create better health for a better world, Mylan may be the place for you. We are a roll-up-your-sleeves-and-get-it-done organization because when we do good, we do well. We offer a wide range of roles that let you use your skills and talents to make a meaningful difference in the lives of billions of people.
Position: Executive – R&D – QA – Injectable R&D
Location: Jigani, Bengaluru, Karnataka, India
Job Description:
Looking for candidates for our Development QA of our Injectable R&D located at Bangalore location. The candidates with 5 to 7 years experience for the mentioned QMS role and responsibilities as our requirement.
- Perform review & approval of the change controls related to master documents, SOPs, instrument / Equipment installations, and material transfers and tracking of the closure of change controls pertaining to R&D
- Perform assessment, approval & closure of Incidents, investigations and CAPAs pertaining to R&D
- Management of Self Inspection Programme by Coordination, Conducting/Tracking at R&D
- Tracking and Trending of Quality matrices, conducting the Quality Review meetings
- Perform the review of Logbooks belonging to R&D functions periodically.
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- Maintain procedures of QA and all functions at R&D in a state of validity and in compliance with the Global policies/Procedures, Regulatory Guidelines
- Review and approval of the SOPs in R&D departments like ARD, FD, PDC, RA, QA & Engineering.
- Ensure a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements
- Evaluation and review of product development activities and their associated documentation along with review and authorization of master documents
- Review of Regulatory documents/summaries that are part of dossiers /deficiency responses/registrations.
Qualification:Â M.Pharm /M.Sc
Experience: 5-7 Years
Salary: Negotiable
Contact Details:
careers@mylan.in, bharathraj.m@mylan.in
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