UCB logo
Pharma DP Manufacturing Specialist
TEMPORARYBulle

Summary

Location

Bulle

Type

TEMPORARY

Explore Jobs

About this role

 

Make your mark for patients


 

Nous sommes à la recherche d’un/e Pharmaceutical Drug Product Manufacturing Specialist pour rejoindre l’équipe Pharma Drug Product Manufacturing (formes sèches), basée dans notre site de production pharmaceutique à Bulle, Suisse.

 

Nous proposons un contrat à durée déterminée (CDM) de 2 ans.

 

Concernant le rôle

 

Dans le rôle de Pharmaceutical Drug Product Manufacturing Specialist, vous  participerez à la gestion du suivi des processus de fabrication, dans le but d’assurer leur Compliance Qualité, leur Sécurité, et leur Fiabilité.

Si vous êtes passionné par les activités de Manufacturing en industrie Pharmaceutique et aimez travailler dans un environnement stimulant et dynamique, nous serions ravis de vous entendre.

 

Vous travaillerez avec…

Votre rôle nécessitera une interaction étroite avec divers départements au-delà du Manufacturing, dont l’Assurance Qualité, la Qualification-Validation, les Equipes Projets, et les départements techniques (automation, maintenance, utilitaires, etc).

 

Vos activités

  • Gérer les déviations de production pharmaceutique et les plans CAPA associés.
  • Gérer les Changes Controls et Actions Items associés.
  • Participer en tant qu'Expert des processus pharmaceutiques dans divers projets, activités de qualification- validation des équipements et processus, etc.
  • Rédaction des documents (SOP, CPV, PQR, Risk assessments, Rapports environnement…)
  • Représentation Production aux audits/inspections.
  • Participer ou mener des plans d'amélioration des processus.

 

Intéressé/e ? Pour ce poste, vous devez posséder la formation, l'expérience et les compétences suivantes :

  • Education : Pharmacien, Ingénieur, ou expérience équivalente.
  • Excellente connaissance des cGxP .
  • Expérience avérée dans la direction de plans d'amélioration.
  • Expertise dans la gestion des écarts de production pharmaceutique et les plans CAPA associés.
  • Expérience en tant qu'Expert des processus pharmaceutiques dans des projets, change-control, CPV, et la validation des processus.
  • La capacité de travailler efficacement dans un environnement très matriciel et dynamique.
  • Faire preuve d'un esprit analytique et d’autonomie.
  • Aisance à planifier, organiser, hiérarchiser et superviser plusieurs tâches en parallèle.
  • Capacité à anticiper les problèmes potentiels et à travailler au dépannage de manière coopérative.
  • Excellente communication.
  • Langues : Français et Anglais courants.

 

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you! 

 

About us 
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science. 

 

Why work with us? 
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential. 

 

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

 

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. 
 
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Other facts

Tech stack
Pharmaceutical Manufacturing,Quality Assurance,Process Validation,Change Control,CAPA Management,Document Writing,Analytical Skills,Problem Solving,Communication,Team Collaboration,Project Management,Risk Assessment,Production Deviations,Process Improvement,Technical Expertise,Planning

About UCB

At UCB, we believe everyone deserves to live the best life they can - as free as possible from the challenges and uncertainty of disease. Our purpose is to support people living with severe central nervous system and immunological conditions by delivering meaningful solutions that go beyond medicine.

We are driven by the experiences of patients and caregivers, and inspired to pursue innovations that create real value - not just in clinical outcomes, but in everyday moments, dreams pursued, and simple pleasures enjoyed. Our ambition is to unlock transformative science and technologies that respond to unmet needs and elevate lives.

From our headquarters in Belgium to nearly 40 countries around the world, we nurture a culture of respect and care. By listening deeply and collaborating across borders and disciplines, we enable cutting-edge research shaped by patients’ needs. Through strong connections with healthcare professionals, partners, and communities, we strive to make a lasting impact - today and into the future.

We're inspired by patients, driven by science.

Team size: 5,001-10,000 employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing
Founding Year: 1928

What you'll do

  • The Pharmaceutical Drug Product Manufacturing Specialist will manage production processes to ensure compliance, safety, and reliability. Responsibilities include handling production deviations, change controls, and participating in process improvement initiatives.

Ready to join UCB?

Take the next step in your career journey

Frequently Asked Questions

What does a Pharma DP Manufacturing Specialist do at UCB?

As a Pharma DP Manufacturing Specialist at UCB, you will: the Pharmaceutical Drug Product Manufacturing Specialist will manage production processes to ensure compliance, safety, and reliability. Responsibilities include handling production deviations, change controls, and participating in process improvement initiatives..

Why join UCB as a Pharma DP Manufacturing Specialist?

UCB is a leading Pharmaceutical Manufacturing company.

Is the Pharma DP Manufacturing Specialist position at UCB remote?

The Pharma DP Manufacturing Specialist position at UCB is based in Bulle, Fribourg, Switzerland. Contact the company through Clera for specific work arrangement details.

How do I apply for the Pharma DP Manufacturing Specialist position at UCB?

You can apply for the Pharma DP Manufacturing Specialist position at UCB directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about UCB on their website.