Supply Chain Documentation Specialist - Beerse, België - Eurofins PSS

Eurofins PSS

Geverifieerd bedrijf

Beerse, België

3 weken geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

Company Description
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Eurofins _is Testing for Life. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing, and in discovery pharmacology, forensics, advanced material sciences and agro-science Contract Research services. Eurofins is also a market leader in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in Biopharma Contract Development and Manufacturing. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. With 58,000 staff across a network of 900 laboratories in 54 countries, Eurofins' companies offer a portfolio of over 200,000 analytical methods. Eurofins Shares are listed on Euronext Paris Stock Exchange.
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Eurofins Professional Scientific Services (PSS_)_ is a global, award-winning insourcing solution. A Eurofins PSS employs and manages full-time analysts, technicians, scientists, and technical support personnel directly at the client facility to provide long term staffing needs while maintaining the same services, expertise, and cGMP compliance available at the Eurofins facility. Eurofins PSS offers excellent career opportunities for people who have a proven track recording in combining excellent technical ability with first class interpersonal and communication skills.

As Clinical Supply Chain Documentation Specialist, you will be working with a well versed and driven service team providing service requests to the Clinical Supply Chain Department.

In this service team you will primarily be focusing on providing support to the Logistics Integrators. In addition, you will also be responsible for handling several service requests and providing functional project support.

You will be responsible for:

Editing, creating and followingup on documents in the documentation system
Creating and followingup Change Controls and Quality Investigations
Troubleshooting and resolving issues.
Facilitating initiation, maintaining overview and following up on annual or final quality reviews
Participating actively in team and client meetings.

Job Requirements

A bachelor degree in Office Management/Business Management or equivalent by experience.
A first administrative work experience is a plus.
An interest for pharmaceutical sciences in an asset.
Outstanding written and communication skills in English. Dutch is nice to have.
Excellent computer & software skills (able to learn to work with different tools and document management systems).
Proficient with Microsoft Office, especially Word and Excel
Showing initiative, assertiveness in followup of requests, proactive approach
Accurate and Detail oriented.
Team player mentality, but with the capacity to work independently.

Additional