Abbott is about the power of health. For more than 125 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.

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The people of Abbott come to work each day with relentless energy, enthusiasm, and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges.

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Position: Manager Quality Assurance

Location: BKC Building, Mumbai, Maharashtra

Job Description:

Accountable for following activities of Contract Operations Quality:

  • Well acquainted with the QRM process and should able to independently perform the QRM assessment.
  • Capable to handle multiple projects and well versed with project management skills
  •  Should have good communications, drafting, and presentation skills.
  • Well versed with Excel/ PowerPoint applications.
  • Well versed with Schedule M/WHO/ D&C acts /cGMP/GLP/CDSCO guidance and should able to ensure compliance at TPM sites.
  • Perform TPM site visits on a scheduled basis to ensure continuous Quality compliance.
  • Well versed with Pharmacopoeia changes and compliance.
  • Should able to conduct an investigation of the Market complaint, root cause analysis, CAPA implementation, and its effectiveness check.
  • Review, assessment, and approval of change controls, deviations, OOS/Failures.
  • To perform a technical assessment of change control, audit CAPA tasks in the QMS system.
  • Should have the ability to impart technical training to quality and operations staff.
  • To perform an assessment of the new sites for cGMP compliance as and when required.
  • To carry out TPM performance monitoring by reviewing the metrics and scorecard as defined in the procedure.

Qualification: B.Sc/B.Pharma, MS/M.Sc/M.Pharma

Experience: Min 10-15 Years relevant Experience either in QA at Internal or 3rd Party Site, Having Exposure/Experience of Quality Risk Management and Quality Project Management is added advantage

Salary: Negotiable

Contact Details:

Click Here to Apply now

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