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Technology Transfer Lead - Drug Product
Job in
6300, Zug, Kanton Zug, Switzerland
Listed on 2026-02-02
Listing for:
Discover International
Full Time
position Listed on 2026-02-02
Job specializations:
-
Healthcare
Healthcare Management, Healthcare Consultant
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
- 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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