Our client is a well-known Biotech company in the Netherlands. At the moment they have a huge workload on the validation team and so are looking for multiple validation engineers to support qualification and validation activities for the next 6 months (extension possible).
RESPONSIBILITIES
- Perform Equipment Qualifications
- Perform Routine Equipment (Re-)Qualification as per Validation Master Plan, maintaining the cGMP compliant state of equipment
- Qualification of new introduced Equipment
- Support introduction of new programs concerning Validation information
- Support and own deviation handling and CAPA’s assigned to the team
- Write qualification protocols, execution and reporting, review of protocols and reports
- Participate in Practical Process Improvement (PPI) project teams
PROFILE
- At least 4-5 years experience in validation within the BioPharmaceutical industry
- Strong knowledge of GMP
- Experience in writing protocols
- Biotech experience is a big pre.
- Selfstarter
- Analytical
- Good knowledge of the English language (dutch is an advantage)
PROJECT DURATION
6 months
PROJECT START DATE
ASAP
PROCESS
Teams Interview with Director Engineering + Validation Manager (1 hour max); decision immediately thereafter.
Get in touch by sending CV and phone number to c.girdwood@panda-int.com ASAP, as interview can take place this week and next!