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Technology Transfer Lead - Drug Product

Job in 6300, Zug, Kanton Zug, Switzerland
Listing for: Discover International
Full Time position
Listed on 2026-02-02
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Consultant
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below

Overview

Technology Transfer Drug Product Development Lead (Biologics)

On behalf of a growing, purpose-driven biopharmaceutical company, we are seeking an experienced Drug Product Development Lead to take technical ownership of Drug Product development, technology transfer, and commercial manufacturing within a global CDMO model.

This senior role provides strategic and hands-on leadership across formulation, fill-finish, and lifecycle management from development through commercialization.

Responsibilities
  • Lead end-to-end Drug Product technical transfers across development, scale-up, and commercial manufacturing, including transfers between CDMOs and commercialization partners
  • Act as Technical Transfer Lead with accountability for planning, execution, risk management, and budget oversight
  • Provide senior Drug Product and formulation SME leadership across programs
  • Lead technical due diligence, selection, onboarding, and governance of CDMOs
  • Provide hands-on oversight of process development, validation, and lifecycle activities at external partners
  • Lead and oversee deviations, change controls, investigations, and CAPAs in collaboration with Quality
  • Provide technical input to regulatory submissions
    , Health Authority interactions, and inspections (e.g. PAI)
  • Serve as Product Steward for assigned molecules with full technical accountability
  • Collaborate closely with Quality, Regulatory Affairs, Program Management, MSAT, and Supply Chain
  • Contribute to the development and continuous improvement of internal standards, SOPs, and technical governance
Candidate Profile
  • Minimum 7 years’ experience in the biopharmaceutical industry with strong Drug Product / biologics exposure
  • Background in MSAT, technical development, manufacturing, or technology transfer
  • Extensive experience working with CMOs/CDMOs in a commercial manufacturing environment
  • Strong knowledge of cGMP and regulatory requirements
  • Academic degree in Pharmacy, Biotechnology, Chemistry, Biochemistry
    , or related discipline
  • Excellent project management and documentation skills
  • Comfortable working in a global, matrix organisation
  • High level of independence, ownership, and accountability
  • Willingness to travel internationally
  • Very good command of English
    ; additional languages are an advantage
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