BioMarin Pharmaceutical Inc. (Swiss Office) · schweiz
BioMarin Pharmaceutical Inc. (Swiss Office) seeks a Senior Scientist 2 for Chemical Development & Manufacturing to lead clinical programs and manage CDMO partnerships in a hybrid role based in Switzerland.
This position sits within the Chemical Development & Manufacturing group of the Drug Substance Technologies function. The incumbent serves as a Partner Team Lead, guiding clinical programs through Process Performance Qualification (PPQ) while overseeing CMC development for synthetic chemistry initiatives across Technical Operations.
Responsibilities
- Coordinate with Drug Substance modality teams, sister groups in TDS, and broader Technical Operations groups.
- Oversee active programs involving Contract Manufacturing and Development Organizations (CDMOs).
- Support group strategy, budget planning, monitoring, and overall program scheduling.
- Collaborate with technical teams to ensure enterprise-wide program timelines are met.
- Identify, evaluate, and assist in selecting new CDMO partners.
- Drive the strategy and performance of the CDMO network and internal functions.
- Anticipate scientific, business, and program challenges, solving problems cross-functionally.
- Manage the drafting and delivery of 3.2.S filing sections and address Health Authority questions.
- Make periodic in-person visits to other BioMarin and CDMO locations.
- Identify, evaluate, and implement new synthetic chemistry technologies.
Requirements
- Bachelor, Masters or PhD level in Chemistry or Chemical Engineering.
- Combined minimum of 9 years of related experience in synthetic molecule, drug substance development environments and CMC DS program management.
- Working knowledge of pharmaceutical regulatory requirements and solid cGMP skills.
- Excellent written and oral communication skills.
- Demonstrated capability at handling multiple programs and projects at one time.
- Agreement to work in a hybrid fashion, spending 2 days per week on average at the local BioMarin site.
- Travel of 20% – 30%.
Nice to have
- Experience in Oligonucleotide development and/or manufacture.
- Familiarity and/or working with ERP and quality documentation systems.
- Post-doctoral experience.
- Business, leadership or related training credentials.
About the company
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions. The company is guided by a purpose to develop medicines that make a profound impact on people’s lives. The role offers an opportunity to join an established, high functioning team with a growth mindset.
- BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
- The company is guided by a purpose to develop medicines that make a profound impact on people’s lives.
- The role offers an opportunity to join an established, high functioning team with a growth mindset.
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