Job Description Summary
Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!Supports the coordination at Global level of the technical evaluations of new products in-licensed from third parties throughout the stage-gate Supply Point Committee (SPC) process across ESO Regions/Platforms
Performs Technical Due Diligence for BD&L projects to ensure capability of suppliers and products.
Provides Technical guidance to support product launches execution.
Job Description
Your Key Responsibilities:
Your responsibilities include, but not limited to:
Technical Evaluation of new products:
- Coordinates at Global level all the technical evaluations of new in-licensed products: assessment of supplier capabilities and process/product robustness to support Supply Point Committee decision
- Ensures that technical evaluations are performed according to prioritized agenda, supporting the Business needs.
- Ensures that assigned evaluations are handed-over to the corresponding ESO MS&T Technical Manager within the Supply Relationship Team and maintains oversight until launch execution.
- Provides regular guidance on the MST BDL evaluation process
- Acts as interface between Global BDL and MS&T representatives within ESO Platforms
Technical due diligence:
- Supports the site selection decisions by providing analysis of technologies and manufacturing risk assessment.
- Performs technical due diligence for selected in-license projects.
Product launches:
- Provides MS&T support for new In-Licensed product launches
What you'll bring to the role:
Minimum Requirements:
Education (minimum/desirable):
- Pharmacist, Chemical Engineer or equivalent
Languages
- Fluent in English.
Relevant Experiences
- Minimum 10 years experience in manufacturing/ manufacturing science
and technology/technical development/Quality
- Demonstrated leadership and accomplishments in a global/matrix environment in the Pharmaceutical Industry
- Proven process understanding (Pharma, GMP, Regulatory aspects).
- Sound experience of data handling and applied statistics
- Proven Project Management experience and problem solving skills
- Experience in Third Partiy manufacturing
You'll receive:
Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well.
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!
#Sandoz
Skills Desired
Change Management, Manufacturing Process Science, Manufacturing Production, Manufacturing Technologies, Process Control, Process Simulation, Quality Compliance, Technical Leadership, Waterfall Project ManagementTop Skills
What We Do
Sandoz is the global leader in generic and biosimilar medicines.
Our Purpose is to pioneer access to medicines for patients globally. We are on a mission to drive innovation in the healthcare industry by freeing up resources sustainably and responsibly while continuing to address global health challenges such as antimicrobial resistance.
We are present in more than 100 countries and our medicines serve some 500 million people every year. We have two main global businesses: Generics - divided between standard generics and complex generics - and Biosimilars.
