Bureau Business Operations Manager

JR France; Paris; Sur place; EUR 100 000 - 140 000; Plein temps

Résumé du poste

Un leader dans l'industrie pharmaceutique recherche un Site Head pour superviser les opérations d'un site de fabrication API. Ce poste stratégique inclut la responsabilité de la conformité, de la qualité et de la gestion financière. Le candidat idéal aura une solide expérience en gestion d'équipe et en optimisation des processus, ainsi qu'une connaissance approfondie des normes réglementaires du secteur.

Qualifications

• 15+ ans d'expérience dans la fabrication pharmaceutique.
• Expérience en leadership senior au sein d'un environnement CDMO ou de fabrication API.
• Expertise démontrée dans des opérations conformes aux GMP.

Responsabilités

• Diriger et gérer les opérations de fabrication API.
• Assurer la conformité avec les exigences réglementaires.
• Gérer le P&L et optimiser les coûts.

Connaissances

Leadership

Gestion de la qualité

Conformité réglementaire

Gestion des opérations

Optimisation des coûts

Formation

Bachelor en Génie Chimique ou Sciences Pharmaceutiques

Master ou Doctorat (préféré)

Description du poste

Social network you want to login/join with:

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Client:

Fraser Dove International

Location:

paris, France

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

724907484905262284832761

Job Views:

1

Posted:

24.06.2025

Expiry Date:

08.08.2025

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Job Description:

Position Overview: The Site Head will lead and manage all operations at our clients API manufacturing site, ensuring the delivery of high-quality products and services to clients within the pharmaceutical and biotechnology sectors. This individual will be responsible for site strategy, operational excellence, regulatory compliance, client satisfaction, and P&L performance. As a senior leader, the Site Head will play a pivotal role in driving the site's growth, fostering a culture of safety, quality, and continuous improvement.Key ResponsibilitiesStrategic LeadershipDevelop and execute the site’s strategic and operational plans in alignment with corporate goals.Serve as the primary site leader, representing the facility internally and externally.Drive growth initiatives, including capacity expansion, new technology implementation, and strategic client partnerships.Operational ManagementOversee all site operations including production, engineering, quality, supply chain, EHS, and facilities.Ensure efficient, compliant, and cost-effective manufacturing processes.Establish and track performance KPIs, driving accountability across departments.Quality, Compliance & EHSEnsure full compliance with cGMP, FDA, EMA, and other global regulatory requirements.Promote a safety-first culture and ensure adherence to environmental, health, and safety standards.Lead site audits, including client and regulatory inspections.People LeadershipBuild, develop, and retain a high-performing leadership team and workforce.Drive a culture of transparency, collaboration, and continuous improvement.Champion diversity, equity, and inclusion across the site.Financial & Commercial OversightManage site-level P&L, budgeting, and capital investments.Drive cost optimization and margin improvement initiatives.Participate in commercial discussions and pricing strategy for site-based services.Qualifications & Experience~ Bachelor’s degree in Chemical Engineering, Pharmaceutical Sciences, or related field (Master’s/PhD preferred).~15+ years of experience in pharmaceutical manufacturing, with at least 5 years in senior leadership roles within a CDMO or API manufacturing environment.~ Demonstrated expertise in GMP-compliant API operations (small or large molecule).~ Strong track record in site leadership, including cross-functional team management and operational scaling.~ Proven experience managing regulatory inspections and client audits.~ P&L ownership experience is essential.