MES Application Manager 100% (m/f/d)
Corden Pharma - A Full-Service CDMO
Infos sur l'emploi
Date de publication :
01 juin 2023Taux d'activité :
100%Type de contrat :
Durée indéterminéeLangue :
anglais, françaisLieu de travail :
Fribourg
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)
Villars-sur-Glâne
- 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
Interested?
Do you require more information?
In case of questions to your application, the position or something else I am very happy to support you.
Contact
Corden Pharma - A Full-Service CDMO