6 часов назад
Head of Drug Product MSAT Synthetics Platform (Pharmaceutical Manufacturing)
114 800 - 153 067€
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Head of Drug Product MSAT Synthetics Platform (Pharmaceutical Manufacturing): Providing strategic, technical, and operational leadership for drug product formulation, process development, engineering, maintenance, quality, and compliance across development, launch, and commercial manufacturing. with an accent on global portfolio strategy, lifecycle management, technology transfer, validation, and regulatory compliance. Focus on harmonizing processes across sites, solving complex manufacturing and quality challenges, and leading continuous manufacturing, PAT, and digital transformation initiatives.
Location: Ambarès, France
Salary: €114,800–€153,067 per year
Company
is an R&D-driven biopharmaceutical company developing medicines and vaccines, with a focus on the immune system and innovative healthcare solutions.
What you will do
- Lead and develop a multidisciplinary Drug Product organization covering formulation, process development, engineering, maintenance, quality, and compliance.
- Define and execute the global Drug Product strategy for synthetic products across late-stage development, launch readiness, and commercial manufacturing.
- Drive formulation and process development for oral solid doses, semi-solids, liquids, and emerging formats.
- Oversee technology transfer, validation, commercial manufacturing support, troubleshooting, root-cause investigations, and process performance.
- Lead lifecycle management, platformization, standardization, harmonization, cost optimization, and continuous improvement across internal sites and external partners.
- Advance continuous manufacturing, PAT, advanced characterization, data-driven monitoring, digital twins, modeling, and data integrity frameworks.
Requirements
- Ph.D. or advanced degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related field.
- Approximately 12 or more years of pharmaceutical industry experience, including senior leadership roles.
- Strong expertise in drug product development and manufacturing, including formulation, process development, scale-up, and validation.
- Deep knowledge of CMC, GMP, and global regulatory frameworks including ICH, FDA, and EMA.
- Experience with regulatory submissions, health authority interactions, commercial manufacturing support, and lifecycle management.
- Demonstrated ability to lead cross-functional teams in a complex global matrix organization.
Nice to have
- Experience managing broad small-molecule drug product portfolios.
- Experience with digital transformation, advanced manufacturing technologies, continuous manufacturing, PAT, and data science applications.
- A strong external network in the pharmaceutical and scientific community.
Culture & Benefits
- Opportunity to contribute to medicines and vaccines that improve health outcomes worldwide.
- Collaboration across R&D, Manufacturing, Quality, Regulatory, Digital, internal sites, and external partners.
- Employee benefit programs may be available.
- Equal-opportunity workplace committed to diversity, equity, and inclusion.
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