Are you experienced with validation documentation (CSV) under GMP regulations and are you looking for a new challenge in Amsterdam? Then this is the vacancy for you, apply now!
Job Description
In this organization, the Validation Officer is responsible for a wide range of documents, surrounding validation, and brings experience in Computerized System Validation (CSV). You work independently on the review of various GMP-documents related to validation procedures, as part of a bigger team. Additionally, you frequently in project teams on implementation of new equipment, systems, building and engineering related matters as well. This biopharmaceutical company frequently collaborates with external parties, meaning that client audits are common, and as part of the QA team, you are involved in these as well. Overall you have a broad position within the QA group, with a focus on (computerized) validations.
Responsibilities
- Review of all types of GMP-validation documentation
- Oversee all qualification and validation processes
- Collaborate in project teams
- Act as SME during audits
- Oversee all CSV matters
Profile
- Minimum of Bachelor in any related field
- At least a few years of experience in GMP
- Validation and CSV knowledge
- Good command of the English language
- Unlimited EU working permit is required.
Benefits
- Long term position, direct contract for 1 year initially
- Salary indication: €4300 - €5500 gross monthly, depending on current experience
- Working hours: Full time, office hours
- Location: Amsterdam
- Travel allowance: 19ct/km or Public transport completely covered;
Vacancy number: 22945
IMPORTANT NOTE: Please do not apply if you do not have a working permit to live and work in the Netherlands. Your application will not be processed.
