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Technical Writer

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The company

Our client is a professional organisation, based in Noord-Brabant Netherlands. Leading biotechnology company in the field of human medicines.

Role description

Assisting as a technical writer in a global project moving SaMD from Medical Device Directive to Medical Device Regulation.

Responsibilities

Rewriting documents from MDD to MDR.

Requirements

- Experience in regulated pharma environment
- Training in MDD to MDR with a recognized regulatory body
- Documentation skills
- Affinity with requirement documentation for Design History file
- Good in verbal and written English

Other information

- Strong handling of time pressure - Project management skills

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Sander Freeke.

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SIRE Information Technology®

Listed by: SIRE Information Technology®
Listed on: 03-12-2018
Country: The Netherlands
Region: Noord-Brabant
Employment: Freelance
Expertise: 0 - 2 years
Location Type: On location
Education: Bachelor
Language: English
Specialisation: Data Science
Sector: Information Technology

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