Senior Validation Manager – Biopharma CQV & GMP

Oxford Global Resources; Hoofddorp; On-site; EUR 81,244 - 97,315; Full time

Benefits offered by this job

Strong professional development opportunities

Leadership growth opportunities

Innovative therapies with high societal impact

Job summary

A leading biopharmaceutical company in the Amsterdam area is seeking a Senior Manager Validation to oversee validation operations and manage CQV projects. The ideal candidate will have a Bachelor's or Master's in Engineering or Life Sciences and 8-10 years of experience in a GMP-regulated environment. They will lead a team, defining validation strategies and ensuring compliance with regulatory expectations. This position offers a project-based contract until the end of the year with a competitive salary and opportunities for professional development.

Qualifications

• 8-10 years of experience in validation within a GMP-regulated environment.
• Proven experience leading validation teams and complex CQV programs.
• Strong communication skills with stakeholders.

Responsibilities

• Lead daily validation operations covering equipment, utilities, facilities, and systems.
• Oversee multiple CQV projects and track progress.
• Manage, coach, and develop the validation team.

Skills

GMP knowledge

Project management

Leadership

Risk-based validation

Education

Bachelor's or Master's degree in Engineering, Life Sciences, or a related technical field

Job description

A leading biopharmaceutical company in the Amsterdam area is seeking a Senior Manager Validation to oversee validation operations and manage CQV projects. The ideal candidate will have a Bachelor's or Master's in Engineering or Life Sciences and 8-10 years of experience in a GMP-regulated environment. They will lead a team, defining validation strategies and ensuring compliance with regulatory expectations. This position offers a project-based contract until the end of the year with a competitive salary and opportunities for professional development.