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Open nowPosted 16 days agoWe saw it 81 min after it went up

Project Manager – Clinical Projects - F/H (CDI)

PolyPeptide France12 open roles

Where
Strasbourg, France
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Your applicationOpen nowProject Manager – Clinical Projects - F/H (CDI)PolyPeptide France · Strasbourg, France
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The clock on this job

Early applications get read.

13.4% of postings close within 7 days. Measured by our own scanner across the market. PolyPeptide France postings stay open a median of 15 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.6%3 days
  3. 13.4%7 days
  4. 21.6%14 days
  5. 36.2%30 days
  6. 59.0%60 days
This job: posted 16 days ago

PolyPeptide France median: 15 days open

The posting

PolyPeptide Group AG et ses filiales consolidées (« PolyPeptide ») est une organisation spécialisée dans le développement et la fabrication sous contrat (CDMO) d'ingrédients pharmaceutiques actifs à base de peptides et d'oligonucléotides.

En soutenant principalement ses clients dans les secteurs pharmaceutique et biotechnologique, elle contribue à la santé de millions de patients à travers le monde. PolyPeptide dessert un marché en forte croissance, offrant des produits et services depuis les stades précliniques jusqu'aux stades commerciaux. Son large portefeuille reflète les opportunités dans les thérapies médicamenteuses à travers divers domaines, avec une grande exposition aux maladies métaboliques, y compris le GLP-1.

Fondée en 1952, PolyPeptide exploite aujourd'hui un réseau mondial de six sites certifiés GMP en Europe, aux États-Unis et en Inde. Les actions de PolyPeptide (SIX : PPGN) sont cotées à la SIX Swiss Exchange.

Nous recherchons pour notre site de Strasbourg dans le cadre d’un Contrat à Durée Indéterminée (CDI) un(e) :

Project Manager – Clinical Projects

Rattaché(e) à la Directrice Program Management, vous serez responsable de la planification, de la coordination et de la livraison des projets dans le respect du périmètre défini, du budget, des délais, des exigences qualité, des contraintes réglementaires et des paramètres de risques convenus. En tant qu’interlocuteur(trice) privilégié(e) des clients et véritable interface avec les équipes internes, vous jouerez un rôle clé dans la réussite des projets, la satisfaction des clients et le respect des engagements de livraison.

Vos principales missions :

  • Piloter les projets cliniques de bout en bout, depuis la phase de planification jusqu’à la livraison, en veillant au respect du périmètre, des coûts, des délais et des exigences qualité définis.
  • Coordonner et animer des équipes pluridisciplinaires, en assurant l’alignement de l’ensemble des parties prenantes et l’atteinte des jalons clés du projet.
  • Être l’interlocuteur principal du client, maintenir une communication proactive, garantir sa satisfaction et traduire ses attentes en actions opérationnelles concrètes.
  • Anticiper et gérer les risques et problématiques projets, afin de sécuriser les délais et livrables tout en facilitant une prise de décision efficace. Assurer également le suivi des coûts (suivi du Scope of Work et gestion des demandes de modification du périmètre).
  • Contribuer à l’amélioration continue grâce au retour d’expérience, au partage des bonnes pratiques et à l’optimisation des méthodes de travail.

Profil recherché :

  • Formation scientifique de niveau Bac +3 à Bac +5 (chimie, pharmacie, biologie ou domaine équivalent)
  • Maîtrise courante du français et de l’anglais, à l’oral comme à l’écrit
  • Expérience en gestion de projet
  • Une expérience dans l’industrie pharmaceutique, au sein d’une CDMO et/ou dans la gestion de la relation client constitue un atout
  • Bonne connaissance des environnements industriels/pharmaceutiques et des BPF/GMP
  • Excellentes compétences relationnelles et de communication, avec une forte orientation client
  • Sens de l’organisation, rigueur, capacité à gérer les priorités et à faire preuve d’agilité
  • Forte capacité d’analyse et de résolution de problèmes, autonomie, esprit d’équipe et aptitude à la collaboration
  • La certification PMP (Project Management Professional) serait un plus

Pourquoi nous rejoindre ?

PolyPeptide offre un environnement de travail dynamique et stimulant, avec l’opportunité de travailler sur une grande variété de projets au sein d’un département engagé. Vous collaborerez étroitement avec l’ensemble des départements de l’entreprise et contribuerez directement à des projets ayant un impact concret sur la santé des patients.

Chez PolyPeptide Group, nous avons à cœur de travailler comme une seule et même équipe.

Poste à pourvoir de suite

______________________________________________________________________________________

PolyPeptide Group AG and its consolidated subsidiaries (“PolyPeptide”) is a focused Contract Development & Manufacturing Organization (CDMO) for peptide- and oligonucleotide-based active pharmaceutical ingredients. By supporting its customers mainly in pharma and biotech, it contributes to the health of millions of patients across the world.

As part of our continued development, we are looking for a Project Manager – Clinical Projects to lead the end-to-end delivery of customer-owned clinical projects.

You will plan, coordinate and deliver projects in line with agreed scope, budget, timelines, quality standards, regulatory requirements and risk parameters. As the key link between customers and internal teams, you will play a direct role in achieving successful project outcomes, ensuring customer satisfaction and delivering on time.

This position will report to the Director of Program Management.

Your mission will be to :

  • Lead clinical projects end-to-end, from planning through delivery, ensuring alignment with agreed scope, cost, timelines and quality requirements.
  • Coordinate and lead cross-functional teams, ensuring alignment across contributors and achievement of key project milestones.
  • Act as the primary customer interface, maintaining proactive communication, driving customer satisfaction and translating customer commitments into operational execution.
  • Anticipate and manage project risks and issues, protecting timelines and deliverables while supporting effective decision-making. Cost follow-up (Scope of Work monitoring, Scope Changes)
  • Drive continuous improvement through lessons learned, best-practice sharing and optimization of ways of working

Profile :

  • Bac +3 /+ 5 in a scientific field (chemistry, pharmacy or biology)
  • Fluent in French and English languages, spoken and written
  • Experience in project management
  • Experience in pharma industry, CDMO and customers interactions is a plus
  • Familiar with industrial/pharmaceutical manufacturing and GMP
  • Excellent interpersonal & communication skills with a strong customer orientation
  • Organized, attentive to details, able to manage priorities and work with agility
  • Strong problem-solving skill, self-motivated, team player and good collaboration skills
  • PMP certification would be a plus

Polypeptide offers a dynamic and exciting work environment with a good opportunity to work with a broad variety of tasks within the dedicated department. You will be working closely with the other departments of Polypeptide.

In the Polypeptide Group, we strive to work as one team.

Why joins us ?

Polypeptide offers a dynamic and exciting work environment with a good opportunity to work with a broad variety of tasks within the dedicated department. You will be working closely with the other departments of Polypeptide. In the Polypeptide Group, we strive to work as one team.

Position available immediately

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