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We envision new ways of providing physicians, pharmacists, and nurses with technologies that not only treat chronic diseases but also work to prevent them. We’re looking for team members who are motivated to learn, grow, and innovate while making a meaningful difference for millions of people around the world.

Position: Supervisor, QA

Location: Ahmedabad, Gujarat

Job Description:

  • To ensure the implementation and maintenance of Current Good Manufacturing Practice (cGMP) standards and all
  • To supervise all IPQA function activity on a daily basis and update to Department Head.
  • To review Master Batch Document (MBD) get approval in advance from Department Head of Production & QA.
  • To ensure the training of new procedures and current guidelines is provided to the IPQA team after discussion/verification of matter by Department Head.
  • To review monthly & weekly production & dispatch plant & ensure smooth implementation of the plan in coordination with Cross Division.
  • To suggest the planning Department in advance, if any change is required.
  • To review Good Documentation practice (GDP)/ Good Manufacturing Practice (GMP) issues, analyze the impact on the product quality, strength, identity, and efficacy and suggest corrective actions, where necessary.

  • To conduct daily morning meetings and review weekly/monthly departmental activity and report the same to Departmental Head.
  • To approve sample/good destruction process and to review and report any gap to Department Head and take corrective and preventive action in co-ordination with respective Department Head.
  • To respond to queries received from international regulatory affairs (IRA department/business partner/regulatory agency and start change procedure and report the queries and response to Departmental Head.
  • To review instrument calibration records & ensure investigations/ CAPA in case of my abnormality observed.
  • To conduct and participate in CAPA meetings and review the summary reports of the same within a defined time period monthly.
  • To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, and take corrective actions.
  • To ensure the investigation for complaints and deviations and CAPA after reviewing instruments.
  • To prepare, review, implement, and update SOP’s according to current regulations systems.
  • To train/update about new procedures and current guidelines or changes in international regulatory requirements.
  • To identify, monitor the deviation/abnormalities in process/documents/systems are captured and resolve them according to Quality Management System.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.

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