Director of Technical Services

JR France; Pays de la Loire; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

Une entreprise mondiale de développement et de fabrication de contrats recherche un Directeur des Services Techniques pour intégrer son équipe de direction sur un site en France. Ce rôle consiste à diriger les transferts techniques et à assurer cette intégration de produits tout en soutenant les initiatives d'amélioration continue pour optimiser la performance opérationnelle.

Prestations

Leadership dans des projets techniques à fort impact

Environnement dynamique et collaboratif

Plan d'investissement stratégique continu

Qualifications

• Minimum 5 ans d'expérience dans un rôle de leadership technique en environnement GMP.
• Connaissance des attentes réglementaires EU/FDA pour l'exploitation.
• Fluide en français et en anglais.

Responsabilités

• Diriger l'exécution des transferts techniques de partenaires globaux vers le site.
• Gérer la validation des processus et la mise à l'échelle technologique.
• Coordonner les équipes interfonctionnelles pour garantir la préparation technique.

Connaissances

Gestion de projet

Leadership

Communication

Formation

Diplôme en ingénierie, chimie ou pharmacie industrielle

Description du poste

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Client:

N&T Life Sciences

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Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

762689820863915622432760

Job Views:

2

Posted:

11.06.2025

Expiry Date:

26.07.2025

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Job Description:

About the Role

We are partnering with a global contract development and manufacturing organisation (CDMO) seeking a Technical Services Director to join the site leadership team at their facility in France.

The Technical Services Director will play a pivotal role in leading tech transfers, validation, and industrial strategy. You will ensure the seamless integration of new products, manage critical projects, and support continuous improvement efforts that elevate operational performance and regulatory compliance.

Key Responsibilities

• Lead the execution of technical transfers from global partners into the site, ensuring on-time, compliant integration of new products and processes.
• Oversee process validation, technology scale-up, and the alignment of technical documentation with GMP and regulatory standards.
• Coordinate cross-functional teams to ensure technical readiness for product launches and lifecycle changes.
• Define and manage the site's multi-year capital investment plan related to technical innovation and capacity expansion.
• Act as a technical authority during audits, regulatory inspections, and customer interactions.
• Embed a culture of continuous improvement, driving process optimization and efficiency initiatives.
• Support quality investigations, deviation management, and CAPA implementation from a technical perspectivees
• Promote and enforce HSE and Quality compliance within the scope of technical services.

Your Background

• Degree in Engineering, Chemistry, Industrial Pharmacy, or a related technical discipline.
• Minimum 5 years of experience in a technical leadership role within a GMP-regulated pharmaceutical environment.
• Proven success managing tech transfers, validation projects, and cross-functional technical initiatives.
• Deep understanding of EU/FDA GMP and regulatory expectations for manufacturing and technical operations.
• Fluent in French and English.
• Strong communication, project management, and leadership skills.

Why Join?

• Join a global CDMO committed to technical excellence and innovation.
• Lead high-impact tech transfer projects in a dynamic, collaborative environment.
• Shape the future of a flagship site with ongoing investment and strategic growth plans.
• Attractive salary fixed €90-120k + variable bonus (negotiable dependent on experience)