VP Operations Non-clinical development and CMC (Switzerland)

Basel - Switzerland

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

At FimmCyte Therapeutics an innovative leader in biotech we are seeking a dynamic and experienced Vice President of Operations focusing on advancing a novel molecule from development candidate to IND approval and beyond. Our company with a close-knit team is committed to advancing cutting-edge therapeutics for large unmet needs. As VP of Operations you will independently drive our endometriosis program through non-clinical development and CMC to ensure the successful progression towards the clinic. This position offers a unique opportunity to experience how a fast paced biotech operates with direct access to executives and the board. That in addition to the chance to drive the end-to-end development process of a novel molecule towards the clinic.

Tasks

Lead overall execution of advancing our antibody program from development candidate (DC) to IND approval
Direct and oversee CMC non-clinical safety pharmacology pharmacokinetics and toxicology studies.
Manage the budget and timelines
Manage and build relationships with global CROs and CDMOs
Ensure effective outsourcing strategies vendor qualification contract negotiations and long-term partnerships.
Interface with potential pharma partners to ensure the timely delivery of milestones
Drive effective program timelines resource allocation and strong project management execution.
Manage regulatory requirements in US EU and Australia

Requirements

Minimum 8 years of experience in project management in small to medium biotech or pharmaceutical organizations >10 years preferred
Minimum 5 years Experience in biologics non-clinical development and CMC
Minimum 1 previous programs taken from DC to IND approval
Proven experience managing CROs and CDMOs globally
Strong project management background with demonstrated ability to deliver results on-time and within scope and budget.
Strongly independent can-do attitude detail oriented striving for maximum quality speed and cost efficiency.
Startup or small biotech experience is a strong plus
Willing to travel 20% of the time globally
Valid work authorization in Switzerland
100% Workload only
January/2026 start

Benefits

Startup team with daily direct access to the executive team
Competitive compensation with stock option plan
Flexible working hours and location (Switzerland or Zurich/Basel)

Tasks

Lead overall execution of advancing our antibody program from development candidate (DC) to IND approval
Direct and oversee CMC non-clinical safety pharmacology pharmacokinetics and toxicology studies.
Manage the budget and timelines
Manage and build relationships with global CROs and CDMOs
Ensure effective outsourcing strategies vendor qualification contract negotiations and long-term partnerships.
Interface with potential pharma partners to ensure the timely delivery of milestones
Drive effective program timelines resource allocation and strong project management execution.
Manage regulatory requirements in US EU and Australia

Requirements

Minimum 8 years of experience in project management in small to medium biotech or pharmaceutical organizations >10 years preferred
Minimum 5 years Experience in biologics non-clinical development and CMC
Minimum 1 previous programs taken from DC to IND approval
Proven experience managing CROs and CDMOs globally
Strong project management background with demonstrated ability to deliver results on-time and within scope and budget.
Strongly independent can-do attitude detail oriented striving for maximum quality speed and cost efficiency.
Startup or small biotech experience is a strong plus
Willing to travel 20% of the time globally
Valid work authorization in Switzerland
100% Workload only
January/2026 start