Validation Coordinator, Contract, Pharmaceutical, Brussels

We have an exclusive contract role available to work onsite with a renowned pharmaceutical company in Brussels, Belgium. This is an excellent opportunity for a French speaking Validation Coordinator to provide support for validation (IO/OQ-PQ) as representative of Commissioning & Qualification (C&Q team).

Please see the following minimum requirements:

- Co-ordinate and manage validations Facilities/Projects C & Q, R & D
- Experience: 1-2 year validation project: Autoclaves/Cold Rooms
- Orientation: University - scientific/technical or equivalent experience
- Knowledge: Word-Office-excel Powerpoint -MS Project-Documentum
- SAP-Techshare-use DOCUMENTUM
- You have good interpersonal skills and good communication in English and French

We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract, alternative market rates are also welcome. Please note there is a job description available on request.

We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will endeavour to get back to you with further information on the role and answer any questions you may have.

Kind regards,

Neha Sharma

Michael Bailey Associates

Keywords: Validation, Commissioning & Qualification, C&Q, pharmaceutical, IQ/OQ-PQ, French, English, GMP, GSP, VMP & PQ protocols, ERC, VSR, Autoclaves, Cold rooms, DOCUMENTUM, SAP, RFV, M-C-QA-TTS, documentary package, project management, R&D, Brussels, Belgium, validation facilities, protocols, equipments, Contract

Michael Bailey International is acting as an Employment Business in relation to this vacancy.