On-site
Part Time
Your Key Responsibilities:
Your responsibilities include, but not limited to:
Responsible for metrics in respective area.
Provide training in respective area.
Supports, initiates and leads continuous improvement activities for the quality assurance systems on site. Document management, change control and training
Ensures that quality assurance systems e.g. document management, change control system, training, escalation management and risk management are in compliance with local and global requirements
Efficient department management in accordance with annual plan (budget / activities / timelines) and defined objectives
Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt
Distribution of marketing samples (where applicable)
Fix-its/Turnarounds.
10+ years of relevant experience.
Functional Breadth.
Project Management.
Skills:
Compliance Requirements.
Continuous Learning.
Dealing With Ambiguity.
Decision Making Skills.
Gxp.
Industry Standards.
Project Management.
Quality Management Systems (QMS).
Quality Standards.
Risk Management.
Self-Awareness.
Technological Expertise.
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!
Sandoz
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