CENEXI

About the Company

Cenexi, a French Contract Development and Manufacturing Organization with its 1,500 employees and 200 million € of turnover, is experiencing a steady growth with its four manufacturing sites (Fontenay-sous-Bois, Osny and Hérouville-Saint-Clair in France, Braine-l'Alleud in Belgium) and one development center for New Product Introduction. Created in 2004, the Cenexi Group is positioned on the very active international market for medicinal products with a major therapeutic indication, drawing on its spirit of innovation and its extensive expertise, both in manufacturing and in product development The arrival of the new top management team induces a new dynamic into the company, in particular by strengthening its sterile expertise which represents 70% of our core business. Cenexi has the production capacities of many dosage forms with strong expertise in cytotoxic products (including hormonal).

Listed Jobs

Company Name

CENEXI

Job Title

RESPONSABLE DE PRODUCTION SECTEUR CONDITIONNEMENT SOLIDE (H/F) - CDD

Job Description

**Job Title:** Production Manager - Solid Dosage Formulation (M/F) - Fixed-Term **Role Summary** Lead and manage solid dosage formulation production operations, ensuring compliance with regulatory standards, quality protocols, and operational efficiency in a highly regulated pharmaceutical environment. **Expectations** Confirmed managerial experience in pharmaceutical production, particularly in solid dosage formulation. Strong understanding of Good Manufacturing Practices (GMP) and pharmacopoeias. Proven leadership and problem-solving skills in a regulated industry. **Key Responsibilities** - Oversee planning, organization, and execution of solid dosage formulation activities. - Allocate human, financial, and technical resources to meet production goals. - Manage team recruitment, training, and performance evaluation. - Ensure adherence to regulatory compliance, quality standards, and production efficiency. - Monitor and analyze production KPIs (productivity, quality, customer service). - Implement corrective actions and drive continuous improvement initiatives. - Coordinate equipment and personnel qualifications. - Define investment requirements for production systems. - Prepare and audit production master plans. - Respond to regulatory audits and compliance inquiries. **Required Skills** - Advanced organizational, analytical, and decision-making capabilities. - Strong leadership and team management experience. - In-depth knowledge of pharmaceutical production regulations (GMP, pharmacopoeias). - Proficiency in production risk assessment, resource allocation, and quality control. - Excellent communication and multilingual skills (fluent English required). **Required Education & Certifications** - Bachelor’s or Master’s degree in Pharmaceutical Engineering, Chemistry, or related field. - Certifications in Good Manufacturing Practices (GMP) or pharmaceutical quality systems preferred.

Fontenay-sous-bois, France

On site

Senior

26-03-2026