GMP Validation Engineer — Biotech CQV Specialist

Panda International; Leiden; On-site; EUR 60,000 - 80,000; Full time

Job summary

A reputable Biotech firm in the Netherlands seeks a Recruitment Consultant to support technical operations leaders in building high-performing biopharma teams. This mid-senior level role focuses on executing essential equipment qualification and ensuring compliance with GMP standards. The ideal candidate has a degree in engineering along with 4-5 years of experience in validation and project engineering within a GMP environment. Interested candidates should send their CV to secure a quick interview process.

Qualifications

• At least 4-5 years experience in validation, CQV, or Project Engineering within a GMP environment.
• Experience with Equipment Qualifications (IQ/OQ/PQ) and Routine Equipment (Re-)Qualification.
• Proficient in English; Dutch is an advantage.

Responsibilities

• Execute and document essential equipment qualification and re-qualification activities.
• Maintain the validated state of existing equipment and qualify newly introduced equipment.
• Support the team in deviation handling and CAPA ownership.

Skills

GMP knowledge

Protocol writing and reporting

Analytical skills

Education

Degree in Engineering or equivalent

Job description

A reputable Biotech firm in the Netherlands seeks a Recruitment Consultant to support technical operations leaders in building high-performing biopharma teams. This mid-senior level role focuses on executing essential equipment qualification and ensuring compliance with GMP standards. The ideal candidate has a degree in engineering along with 4-5 years of experience in validation and project engineering within a GMP environment. Interested candidates should send their CV to secure a quick interview process.