Senior Scientist 2, Chemical Development & Manufacturing

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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