Serialisation project manager regulatory affairs
Location: BelgiumThe Company
They are well known for their mission "focusing on creating value for people living with conditions". Their business is strong and are very excited about the progress in our early research pipeline.Role Description
Every medicine needs to be traceable. In your role are serialisation specialist you will manage the artwork and labeling changes around the serialisation process. You will be the first point of contact or their artwork and labeling and RA team! It's a great project that has a focus on an international level.Responsibilities
They needs someone who will be responsible for the serialisation team for at least 1 year! The right specialist is gone be responsible for managing artwork changes and the labeling responsibilities. He is gone be the single point of contact of the RAO and Artworkers and labeling team. You are gone fulfil a coordinator role.Requirements
- Bachelor degree or Masters degree within the (bio)pharmaceutical industry or engineering- English is a must and French is a Pre (plus)
- Knowledge of the European regulations of serialisation.
- pharmaceutical background RA affairs background
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
Job Description
The Company
They are well known for their mission "focusing on creating value for people living with conditions". Their business is strong and are very excited about the progress in our early research pipeline.Role Description
Every medicine needs to be traceable. In your role are serialisation specialist you will manage the artwork and labeling changes around the serialisation process. You will be the first point of contact or their artwork and labeling and RA team! It's a great project that has a focus on an international level.Responsibilities
They needs someone who will be responsible for the serialisation team for at least 1 year! The right specialist is gone be responsible for managing artwork changes and the labeling responsibilities. He is gone be the single point of contact of the RAO and Artworkers and labeling team. You are gone fulfil a coordinator role.Requirements
- Bachelor degree or Masters degree within the (bio)pharmaceutical industry or engineering- English is a must and French is a Pre (plus)
- Knowledge of the European regulations of serialisation.
- pharmaceutical background RA affairs background
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control / Production Audit