01Lead high-impact initiatives - including technology transfers, validation activities, new product introductions, major process changes, and cross-functional issue resolution.
02Connect complex technical and manufacturing topics to their business, quality, regulatory and supply implications.
03Align local and global teams including Manufacturing, Quality, Regulatory Affairs, Supply Chain, Engineering, and Global Manufacturing Science & Technology (Global MSAT).
04Drive pragmatic, scientifically sound and compliant solutions to protect batch viability and supply continuity.
05Coach and mentor fellow Site Product Managers, supporting knowledge sharing and continuous development of project management practices.
Exigences
↳University degree in Life Sciences, Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or a related scientific discipline; an advanced degree - Master-s or PhD - is an asset.
↳5+ years of experience in biopharmaceutical manufacturing, Manufacturing Science and Technology, technology transfer, validation, quality, or a related technical function within a GMP-regulated environment.
↳Proven ability to lead complex, cross-functional projects end-to-end.
↳Strong understanding of biotech manufacturing and product lifecycle management across Drug Substance, Drug Product / Fill & Finish, and Final Product / Packaging.
↳Fluency in both French and English.
Avantages
＋Project management certification or advanced training - such as PMP, Agile, or equivalent - is an asset.
