Analytical Method Validation Specialist
For this booming Biotech client, I am looking for a Senior Validation Specialist with experience in Analytical Method Validation. Initial project is 6 months, also open for candidates that are looking for a permanent position.
- Overseeing process and methods verification / qualification / validation deliverables
- Review and approve the process performance qualification (PPQ) Readiness plans
- Review and approve the risk assessments related to process and method validation
- Review and approve PPQ, method validation master plan protocols and reports
- Provide support in all quality-related issues, including GMP regulations, compliance with internal SOPs
- Degree in LifeSciences and preferably around 5-10 years of experience.
- Experience in Analytical Method Validation and background in QA
- Understanding of cGMPs, GAMP, ICH Q9, Q7A and validation practices
- Experience on QA related quality system deliverables (CAPA, Change Control) and validation deviations and changes
· ASAP (flexible)
· 6 months with high change of extension OR temp-to-perm
If you’re interested in the above description, please apply with your CV and a letter of motivation by clicking on the ‘apply’ button below. For further information, please contact Merel van Os at +31 (0)20 20 44 502 or by email at email@example.com