Job Description Summary
Job Description SummaryJob 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)
What youll bring to the role:
Functional Breadth.
Minimum 8 years of relevant experience.
QC/ QA in pharmaceutical ind./ biotech with environmental monitoring & collaborating across boundaries.
Why Sandoz
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!
The future is ours to shape!
Skills Desired
Continued Learning Dealing With Ambiguity Gmp Procedures Qa (Quality Assurance) Quality Control (Qc) Testing Quality Standards Self-Awareness Technological Expertise Technological IntelligenceRequired Experience:
IC