Validation Engineers (CQV)

Location Netherlands
Discipline: Biotechnology
Job type: Temporary/Freelance
Contact name: Caitlin Girdwood

Contact email: c.girdwood@panda-int.com
Job ref: 18915
Published: 23 days ago

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!