Sandoz Job Opening for Specialist – Quality Operations position – Apply Now
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
Your Key Responsibilities:
Your responsibilities include, but not limited to:
- Receive and review the initiated complaints in the QMS tool. Process / Send technical complaints to CMO / Supplier for investigation.
- Co-ordinate for complaint sample availability, additional information from Country Organization (CO) to CMO (Contract Manufacturing Organization) and vice versa as and when required.
- Periodic follow up of complaints with supplier for timely investigation. Perform queries in QMS tools like GxQEM etc. as per the procedures.
- Reviewing of supplier investigations and completing it in QMS tool for complaints delegated to GQSI. Perform the role of QA approver for complaints delegated to GQSI.
- Tracking and extension of complaint / actions as per the requirements. Complete the assigned tasks as per business need.
- Management of Child records such as Investigation, Communication action etc. as per the requirement.
- Participate in meetings / discussions between sites and suppliers over supplier complaints as and when required.
- Perform Quarterly complaint/ deviation trending and reporting. Evaluation of Signals and further management in QMS tool.
What you’ll bring to the role:
Essential Requirements:
Work Experience:
- Proven experience of 3+ y in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances/ products/ medical devices
- GxP knowledge, Basic IT knowledge
- Experience of working closely with the global stakeholders
Languages :
- Proficient in English (written and spoken)
- Good communication, presentation, and interpersonal skills
You’ll receive:
Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well.
APPLY HERE
https://chat.whatsapp.com/DO9PMPj2H3K4SikyHri52x
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