Validation Specialist

Validation Specialist - Netherlands

Annual Salary: €60,000 - €65,000
Contract Type: 6 -month contract
Work Schedule: Full-time hybrid role, minimum 3 days on-site Hoofddorp, Netherlands.

Description: Join a leading biopharmaceutical company dedicated to innovation in cancer treatment. We are seeking a dedicated Validation Specialist to support routine validation activities and validation projects.

Responsibilities:

• Perform routine validation activities and support validation projects.
• Create and execute commissioning, qualification, and validation protocols (CP/IQ/OQ/PQ), including resolving exceptional conditions.
• Conduct temperature mapping and other validation activities.
• Investigate and implement corrective actions related to protocol exceptional conditions.
• Coordinate validation instrument inventory calibrations and/or certifications.
• Support vendor protocol executions as necessary.
• Create Computerized System Validation (CSV) documents, including risk assessments, validation project plans, user acceptance tests, and reports.
• Collaborate with Quality Engineering to develop CSV strategies and procedures.
• Provide guidance and execute strategies for computerized system, equipment, utility system, and facility commissioning and qualification during project planning and development phases.
• Review technical documentation, including protocols, summary reports for CSV and CQV lifecycle documentation, and other testing and validation SOPs.
• Report the status and progress of qualification activities or projects to the Leadership team.
• Manage contractors performing equipment and system commissioning, qualifications, and validation.
• Develop or review technical specifications documents necessary for CQV lifecycle documentation.
• Perform investigations and implement corrective actions related to CAPAs and deviations.
• Additional duties as assigned.

Qualifications:

• MBO level 4 with at least 6 years of experience or HBO with at least 4 years of experience.
• GMP experience in pharmaceutical or relevant industries.
• Validation experience.

Additional Information:

• Working Hours: Business Hours (40hrs/week), with flexibility when required.
• On-site Days: Minimum 3 days on-site.
• Extension Possibilities: Yes.
• Language Skills: English mandatory, other languages beneficial.

Join us in advancing cancer treatment through precise validation and compliance activities.

Send your CV to cosman@i-pharmconsulting.com or call +442075510737. Refer someone and earn a £500 referral bonus upon their successful placement.

We welcome all qualified candidates and are committed to an inclusive environment. We look forward to hearing from you!