Responsable Développement Analytique R&D

Ceva Santé Animale; Louverné; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A global leader in animal health is seeking a Head of Analytical Development. Located in Louverné, you will ensure the analytical development of pharmaceutical products. Your responsibilities include managing a team of analytical technicians, developing methods for product analysis, and ensuring compliance with international guidelines. Ideal candidates have a Master’s or PhD in analytical chemistry and at least five years of relevant experience. Comprehensive benefits are offered, including meal vouchers and variable remuneration.

Prestations

Fixed + variable remuneration

Meal vouchers

RTT (reduced working hours)

Profit-sharing

Mutual insurance

Qualifications

• 5+ years of experience in analytical development in a pharmaceutical setting.
• Experience managing a team of analytical technicians.
• Excellent knowledge of ICH, VICH, FDA, EMA guidelines.

Responsabilités

• Ensure analytical development in accordance with specifications.
• Manage team activities and provide technical support.
• Draft pre-validation protocols and reports.
• Coordinate compliance activities in the analytical laboratory.

Connaissances

HPLC proficiency

Communication skills

Analytical and synthesis skills

Teamwork

Formation

Master’s degree or PhD in analytical chemistry

Outils

HPLC

UPLC

GC

Description du poste

Head of Analytical Development, R&D

The success of a company depends on the passionate people we partner with.

Together, let's share our talents.

As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing, producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.

We are committed to ensuring the highest possible level of care and well‑being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.

Indeed, Our Together, Beyond Animal Health vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.

As part of our Diversity, Equity and Inclusion policy, Ceva Animal Health is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.

Your missions :

Located 1 hour from Rennes and Le Mans and 1.5 hours from Paris by train, the Ceva Laval Campus is our centre of excellence for companion animals (dogs and cats).

Within the Research and Development department of this Campus, we are looking for an Analytical Manager to strengthen the analytical development team. As part of the pharmaceutical R&D team, you will contribute to the development of future pharmaceutical products for the Ceva group.

Your responsibilities will include :

• Ensuring the analytical development of the products entrusted to you, in accordance with development plans and specifications. This involves developing methods for dosing and characterisation using HPLC, UHPLC, GC, KF, IR, UV, dissolution, etc., either in‑house or through subcontractors.
• Working closely with the formulation department (to develop the formula) and the various project team members: Project Manager, Industrial Development, EU and US Regulatory Affairs Manager, etc.
• Managing a team of analytical technicians (planning their activities, providing technical support, etc.).
• Pre‑validate analytical methods and draft pre‑validation protocols and reports in accordance with international guidelines (ICH, VICH, FDA, EMA, etc.).
• Manage the transfer of analytical methods to and from internal QC laboratories or international subcontractors (drafting protocols and reports, choosing acceptance criteria, etc.).
• Coordinate activities related to cGMP compliance in the analytical laboratory (drafting procedures, monitoring CAPA, deviations, etc.).
• Draft the analytical documentation required for new marketing authorisation applications and monitor technological and documentary developments concerning pharmacopoeias.

Education and experience

You have a five‑year degree, Master’s degree or PhD in analytical chemistry.

You have at least five years of successful experience in this role.

Technical skills

Proficiency in HPLC / UPLC techniques (UV detection, MS) and dissolution testing.

Essential experience in managing analytical technicians, preferably acquired in a pharmaceutical setting in a cGMP environment.

Excellent knowledge of the prerequisites for developing HPLC‑UPLC methods and dissolution testing.

Behavioural skills

You are an excellent team player with good adaptability and communication skills.

You are rigorous, organised and interested in integrating international standards into analytical development processes.

Autonomy, rigour, coordination, analytical and synthesis skills, and good interpersonal skills are your assets for success in this position.

Your benefits at Ceva

• Fixed + variable remuneration
• Meal vouchers (face value €10.25, 60% of which is paid for by the company)
• RTT (reduced working hours), Time Savings Account
• Profit‑sharing, incentive schemes, attractive company savings plan
• Mutual insurance and provident fund
• CSE benefits and an association offering activities on campus (yoga, fitness, cooking classes, creative arts, etc.) and off campus (after‑work events, indoor football tournaments, etc.)

Wondering what our campus looks like? Here it is : https://www.youtube.com/watch?v=NF8k6qsxj4s&t=7s

And what is Laval like? https://www.calameo.com/read/d94cecbcde40

Formation et expérience

Vous êtes titulaire d'un Bac +5, Master ou doctorat en chimie analytique

Vous avez une expérience réussie d'au moins 5 ans dans la fonction

Compétences techniques

• Maîtrise des techniques HPLC / UPLC (détection UV, MS) et des essais de dissolution
• Expérience impérative en management de techniciens analystes, acquise de préférence en milieu pharmaceutique dans un environnement cGMP.
• Excellentes connaissances des prérequis au développement de méthodes HPLC‑UPLC et à la mise au point d'essai de dissolution.

Compétences comportementales

• Vous disposez d'un excellent esprit d'équipe et de bonnes capacités d'adaptation et de communication.
• Vous êtes rigoureux / sont, organisé(e) et vous êtes intéressé(e) par l'intégration des référentiels internationaux dans les processus de développement analytiques.
• Autonomie, rigueur, coordination, capacité d'analyse et de synthèse, bon relationnel sont vos atouts pour réussir à ce poste.

Vos avantages chez Ceva

• Rémunération fixe + variable
• Tickets restaurant (valeur faciale 10,25 euros dont 60% pris en charge par l'entreprise)
• RTT, Compte Épargne Temps
• Intéressement, Participation, Plan Épargne Entreprise attractif
• Mutuelle et prévoyance
• Avantages CSE et présence d'une association proposant des activités sur le Campus (yoga, fitness, cours de cuisine, arts créatifs) et hors Campus (afterwork, tournoi de foot en salle)

Vous vous demandez à quoi ressemble notre campus ? Le voici : https://www.youtube.com/watch?v=NF8k6qsxj4s&t=7s

Et Laval, c'est comment ? https://www.calameo.com/read/d94cecbcde40