Why join Cenexi
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Join a dynamic CDMO where you will have 360° responsibility and real autonomy to prioritise operations and to propose improvements and investment initiatives. You will face constant, client‑centric challenges that matter, supported by significant ongoing investments to modernise facilities and scale capabilities. We offer a comprehensive compensation package, a mandate to lead measurable transformation, and a motivated, engaged team committed to quality and client success. This role gives you the chance to lead half of the site’s industrial footprint and make a direct, visible impact on profitability, compliance and customer satisfaction.
About the Cenexi Group
Cenexi is a French CDMO established in 2004, specialised in sterile products and a trusted partner to innovative biotechs. The group provides formulation, development, manufacturing and filling services for complex pharmaceutical products, with recognised expertise in handling controlled substances, high‑potency compounds (allergens, hormones, oncology) and biologics (monoclonal antibodies, ADCs and peptides). Cenexi combines deep technical know‑how, continuous investment in modern facilities and a client‑first approach, and is strengthening its position in advanced biologics manufacturing.
About the role
As Manufacturing Director, you will manage the industrial heartbeat of a leading CDMO. You will define and deliver the site’s industrial strategy, lead all production activities (manufacturing, packaging, operational support) and shape a high‑performing organisation in a GMP environment. This is a visible, high‑impact leadership role responsible for end-to-end cGMP manufacturing, regulatory readiness, operational performance and customer satisfaction.
Your key Responsibilities
* Lead and oversee cGMP manufacturing operations
* Manage and develop a large-scale manufacturing organization (~150FTEs)
* Drive site performance, scalability, and operational excellence during a period of expansion
* Partner closely with Quality and senior leadership to ensure inspection readiness and compliance
* Play a key role in regulatory inspections (FDA and others), including direct involvement during audits
* Act as a primary point of contact for clients during site visits and manufacturing discussions
* Implement and drive continuous improvement and LEAN manufacturing systems
* Lead organizational growth, including team scaling, structure, and talent development
* Member of the site leadership team
Your profile
You bring 12–15+ years of industrial manufacturing experience with strong GMP / pharmaceutical credentials and a proven track record leading large teams (≥100). You combine operational rigour and industrialisation expertise (experience with lyophilisation is a plus) with a transformational leadership style: strategic thinker, decisive, influential and people‑centred. You are fluent in French and English and hold a Master’s or engineering degree in pharmacy, chemistry, engineering or equivalent.
How to apply
Send your CV and a short cover note to with subject Manufacturing Director — [Your Name]. xphnsxz Applications are reviewed on a rolling basis.