Do you love to make sure that your organisation operates compliant to GMP regulations? Then this is a very nice position for you!
Job Description
In this position you work at one of our largest clients, a leading pharmaceutical company, as a QA officer with a focus on internal auditing to ensure compliance with internal operating procedures and international pharmaceutical regulations such as GMP.
Responsibilities
- Internal auditing of procedures, data, (computer) systems, etc
- Review production and analytical documentation
- Review documentation regarding regulatory compliance
- Communication of audit findings with stakeholders
- Perform (supervised) audits to ensure regulatory compliance and generate reports
Requirement
- Finished relevant education in the field of Laboratory science or related
- Experience in the pharmaceutical industry or regulatory agency
- Experience with working in a GMP environment
- Excellent communication skills (oral/written)
- Excellent interpersonal skills
Benefits
- Employment: Temporary for a period of one year with Oxford Global Resources Solutions. Extension is possible
- Salary indication: From approximately € 3250 to € 3750 gross per month
- Working hours: full time
- Location: Region Den Bosch
Vacancy number 16095
