Arras
ARTO is currently supporting a leading biopharma manufacturer in the search for a Head of MSAT Consultant to ensure continuity across a critical manufacturing site. This is a senior leadership role responsible for overseeing industrialisation, validation, and process performance across upstream, downstream, and sterile fill & finish operations. Key Responsibilities 🔧 • Ensure continuity of activities across industrialisation and validation (equipment, process, cleaning, environment), • Lead commissioning of workshops and lifecycle management projects (from validation design through to execution), • Guarantee process control and product compliance, • Maintain industrial performance by supporting production and integrating performance into projects, • Secure interfaces between production, quality, and support functions, • Contribute to stabilisation and targeted improvement of existing practices, • Prepare conditions for a smooth transition to the future leader Scope of the Role 👥 • Manage and lead the team, ensuring high levels of engagement and performance, • Oversee activities in line with site standards (governance, reporting, KPIs, prioritisation), • Participate in the site management committee, • Ensure compliance with GMP, HSE, and company standards, • Collaborate with internal stakeholders across site and group functions Environment 🧪 • Site operates across plasma upstream, downstream, and sterile fill & finish (vials) Requirements 🎯 • Demonstrated experience in pharmaceutical production of complex products (biologics, sterile, etc.), • Strong managerial and project management experience, • Fluent professional French (essential), • Ability to work minimum 4 days on-site (Northern France) 💬 𝐈𝐧𝐭𝐞𝐫𝐞𝐬𝐭𝐞𝐝? Apply here or message me directly.