Specialist - Quality Operation GQS-I

Job Description

Your Key Responsibilities:

Your Responsibilities Include, But Not Limited To

• Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance
• Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review
• Support OpEx improvement projects Qualified Person – Executes batch release in compliance with registration
• Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt
• Distribution of marketing samples (where applicable)
  
  

Essential Requirements

What you’ll bring to the role:

• Functional Breadth.
• Minimum 8+ years of relevant experience.
• QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &.
• Collaborating across boundaries.
• cleanliness zones.
  
  

Skills

• Continuous Learning.
• Dealing With Ambiguity.
• Gmp Procedures.
• QA (Quality Assurance).
• Quality Control (Qc) Testing.
• Quality Standards.
• Self-Awareness.
• Technological Expertise.
• Technological Intelligence.
  
  

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, 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 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 supported!

Join us!

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