Technology Transfer Project Manager

Overview

In this role you lead technology transfer and industrialization efforts for small molecule products, ensuring robust technical oversight across internal and external manufacturing sites. You will coordinate cross-functional teams to drive project execution, manage risks, and support supply continuity. You help shape scalable processes and maintain regulatory and GMP alignment in a fast-paced environment. This position offers impact across commercialization, lifecycle management, and continuous improvement within a global pharma setting.

Responsabilità Lead technology transfer projects for small molecule drug products across internal and external manufacturing sites

Coordinate TT master plans, protocols, gap assessments, process descriptions, validation strategies

Support process scale-up, PPQ, and readiness of manufacturing documentation

Troubleshoot technical issues, propose solutions, and guide SME/CDMO decision-making

Ensure alignment with CMC, regulatory commitments, and change control processes

Provide technical oversight for commercial processes across solid dosage, semisolid, sterile and non-sterile forms

Review and approve manufacturing documentation (batch records, SOPs, control strategies)

Analyze manufacturing data, identify optimization opportunities

Support process validation, OOS/OOT investigations, deviation resolution, and CAPA definition

Drive cross-functional teams to ensure timely delivery of project milestones

Coordinate information flow with internal and external stakeholders for transparency

Manage timelines, budget, risks, mitigation plans, KPIs, and governance reporting

Foster collaboration across functions and geographies while maintaining GMP/regulatory awareness

Requisiti fondamentali Min. 6-7 years’ experience in MSAT, Technical Operations, Technology Transfer in pharma

Solid understanding of manufacturing processes for solid oral dosage forms, semisolids, and sterile/non-sterile liquids

Experience managing technology transfer, process validation, and commercial manufacturing support

Competence in reviewing technical documentation and scientific/quality evaluations

Strong knowledge of ICH guidelines, GMP, validation principles, and change control

Ability to work under pressure, manage multiple priorities, and operate in cross-functional settings

Experience with external manufacturing management (CMOs/CDMOs) is a strong plus

QC/QA or CMC background considered a significant advantage

Strong analytical mindset

Problem-solving and autonomous decision-making

Ability to work with global teams and adapt to different cultures

MSAT and technology transfer leadership

Process validation and PPQ

GMP compliance and regulatory frameworks