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Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
  • Quality Assurance oversight for Packdown activities and Packdown shop floor compliance.
  • Responsible for ensuring the processes of Supplier qualification procedure in Jigani site (i.e., evaluation of suppliers, Compliance of LS policy, supplier audits, Quality agreements etc...).
  • Responsible for ensuring that processes for the Deviation management are established, implemented, and maintained for the site.
  • Responsible for verifying the allotment of deviation / OOS CAPA from User departments, follow up for completion and ensuring the compliance of CAPA for closure. HOQMS (health of Quality management system) shall be ensured.
  • Responsible for ensuring that processes for the training management activity across the site (i.e., Allotment in HR4You, Training curriculum for new employees, Ensuring the compliance of Training SOP procedure).
  • Reporting to Quality assurance head on the performance of the Quality Management System and any need for improvement in the Manufacturing.
  • Uploading of relevant QMS documents in ManGo system.
  • Providing Line clearance to pack down area.
  • Performing the vendor audits of raw material/ packaging material suppliers and qualification of suppliers and vendors as applicable & Preparation of quality agreements with the suppliers and its maintenance.
  • Responsible for meeting Quality Metrics set for the organization.
  • Providing data and support for weekly, monthly reports and Quality management reviews.
  • Conduct internal audits ensuring CAPA proposal and completion on time wherever required.
  • Preparation, review and approval of procedures and its implementation.
  • Conduct trainings to the CFT on new procedures and any changes in existing procedures wherever applicable.
  • To complete any other activity assigned by Head Quality Assurance or management personnel.


What we offer:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!
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Deadline: 23-06-2024

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