Managing Director (m/f/d) – Drug Substance CDMO

Introduction Corden

Pharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DP), and packaging. With around 3,000 employees worldwide, we help pharmaceutical and biotech companies manufacture medicines with the ultimate goal of improving people’s lives. Our network, spanning Europe and the US, provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well‑being.

Our People Vision We strive for excellence. We share our passion. Together, we make a difference in patients’ lives.

Your Opportunity We are looking for a Managing Director to lead our Drug Substance site in Chenôve, France. In this role, you will have full responsibility for the site (approx. 220 employees) including P&L ownership, operational excellence, and long-term strategic development. You will play a key role within the global business unit network, driving business growth, customer satisfaction, and operational performance in a highly dynamic CDMO environment.

Strategic Responsibilities

Define and execute the site strategy in alignment with the global business unit.

Drive business growth by supporting commercial activities and expanding the customer portfolio.

Ensure long‑term competitiveness through continuous improvement and operational excellence initiatives.

Lead and develop the organization, fostering a strong performance and collaboration culture.

Own and steer the site master plan and investment strategy (CAPEX).

Build strong relationships with key customers and represent the site in strategic meetings and business reviews.

Operational Responsibilities

Full accountability for site performance, including revenue, EBITDA, and financial results.

Ensure reliable and compliant manufacturing operations (on‑time, in‑full, right‑first‑time delivery).

Guarantee compliance with GMP, regulatory, quality and HSE requirements.

Oversee day‑to‑day site operations and production planning.

Drive high customer satisfaction in close collaboration with PMO and operational teams.

Ensure adherence to Corden

Pharma’s Code of Conduct and ethical standards.

Education

Ph

D (or equivalent) in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field.

MBA or additional business qualification is a plus.

Experience & Background

Extensive leadership experience in the Drug Substance CDMO environment.

Proven track record in managing large‑scale c

GMP pharmaceutical manufacturing sites.

Strong P&L responsibility experience.

Experience operating within complex, matrix organizations.

Commercial mindset with strong customer orientation.

Languages

Fluent in French and English; additional languages are an advantage.

Leadership & Competencies

Strong business acumen and results orientation.

Proven ability to lead and develop high‑performing teams.

Excellent stakeholder management and influencing skills.

Strategic mindset combined with a hands‑on, execution‑driven approach.

High level of integrity, ownership, and resilience in fast‑paced environments.

What we offer

An attractive workplace with a high level of responsibility.

Dynamic and exciting work environment.

Cantine.

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