MES Application Manager 100% (m/f/d)

Corden Pharma - A Full-Service CDMO

Corden Pharma - A Full-Service CDMO


Infos sur l'emploi

  • Date de publication :

    01 juin 2023
  • Taux d'activité :

  • Type de contrat :

    Durée indéterminée
  • Langue :

    anglais, français
  • Lieu de travail :


CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2’600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives.

Our network in Europe and the US offers flexible and specialized solutions across five technology platforms: Peptides, Lipids & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients.

To strengthen our Global team in Basel (CH) or Plankstadt (Germany) we are looking as soon as possible for an

MES Application Manager 100% (m/f/d)

  • Fribourg
  • ASAP
  • Full-time
  • Permanent

Main activities and responsibilities

  • Plan, manage and implement changes / projects across departments and aligne with all stakeholders
  • Responsible for collecting and harmonizing the business requirements
  • Responsible for the contract(s) and performance of the System providers and consultants
  • Primary contact with System providers and consultants in order to translate requirements into solutions
  • Manage global quality documentation & training of the System
  • Responsible that the key users are able to perform the tasks by providing guidance, knowledge, training and overall support.
  • Support local stakeholders in optimising the use of the System
  • Support complex issue troubleshooting
  • Coordinates the escalation process for problem solving with different parties
  • Manage projects for new processes implementation
  • Define and implement process standardization
  • Lead the MBR process design
  • Drive the MBR validation activities
  • Budget tracking of the System
  • Business and System owner cycle reviews.

Your Profile

  • Bachelor’s degree in technical field
  • Certification and experience with MES a must, MES PAS-X a plus 
  • 5 years’ experience in operation function within the pharma industry or similar industry (i.e. food, medical devices,)
  • Minimum 3 years’ experience in working in IT close environment and process harmonization and optimization
  • Fluent in English & French
  • Project management experience.

What we offer

  Retirement Pension Plan
  Dynamic and exciting work environment
  Parking Lot
  Training and Continuing Education
  Home Office


If you enjoy working in a team and are interested in a varied area of responsibility, if you think and act beyond your own area of responsibility, then you should join our team.

Do you require more information?

In case of questions to your application, the position or something else I am very happy to support you. 



  • Corden Pharma - A Full-Service CDMO