If you can easily structure workflow and write eloquent and clear instructions and enjoy making Standard Operating Procedures, this could be a very interesting position for you!
Job Description
In this position of GMP Documentation Writer you write SOPs, templates and assist with data extraction of GMP data. A versatile administrative position at a global pharmaceutical company.
Responsibilities
- Write User Requirement Specifications, qualification protocols
- Update documentation systems
- Extract data (e.g. SAP data) when required
- Support projects (e.g. qualification, etc)
Requirement
- Minimally finished HBO or MSc education, eg in Life sciences or process engineering
- Work experience in pharma and GMP
- Experience writing documents such as SOP's is required
- Experience with scientific writing is a plus
- Very good skills with MS Word. Templates and layout settings have no secrets for you
- You have very good understanding of English, both written and spoken
- You can work independent and have no problem working remote (during covid) and partially on site (after covid)
Benefits
- Employment: Temporary for a period of 7 months with Oxford Global Resources Solutions. Project duration is minimal 1 year
- Salary indication: From approximately € 3000 to € 4500 gross per month
- Working hours: full time
- Location: Region Nijmegen
Vacancy number: 16403