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4 weken geleden
Job Title: CQV Engineer (Associate Director)
Contract Duration: 12 Months
Location: Netherlands
As the Qualification Engineer (Associate Director), you will be entrusted with the responsibility to lead and shape the engineering efforts that drive the success of the site. You’ll oversee the performance of critical systems and equipment, ensuring they meet rigorous quality standards and industry regulations.
You’ll guide teams through complex capital projects and continuous improvements, making a tangible impact on both operational efficiency and the health of millions worldwide.
A great opportunity if you have In-depth understanding of qualification protocols, regulatory standards, and engineering best practices, looking for an environment to leverage and drive change
Lead and manage the site engineering team, ensuring design, installation, and maintenance of infrastructure, utilities, and facilities in compliance with operational safety standards.
Oversee the qualification process for new and modified equipment, systems, and facilities, ensuring compliance with regulatory standards (e.g., Manage capital projects and engineering improvements, ensuring timely, budget-compliant execution while meeting regulatory needs.
Collaborate with cross-functional teams, including operations, quality, and production, to align on qualification strategies and compliance.
Ensure full compliance with local, state, and federal regulations, leading efforts to mitigate risks related to engineering activities.
Promote a culture of continuous improvement, implementing process enhancements to optimise engineering and qualification practices.
Hire, mentor, and develop engineering staff to achieve site objectives, providing leadership and professional growth opportunities.
Bachelor’s degree in Engineering (e.g., Mechanical, Electrical, Chemical, Industrial, or related discipline).
Strong engineering background with leadership experience in regulated environments.
Proficient in qualification and validation of equipment and facilities.
Proven ability to lead large-scale engineering projects and manage multiple priorities.
cGMP, FDA, ISO) and best engineering practices in manufacturing.
An exciting opportunity to join a dynamic team, contributing to global health efforts while leading innovative engineering projects.
