Compliance Manager

3 weken geleden

Leiden, Nederland Talentor Netherlands Voltijd
Join the organization to create a safer and healthier world through vaccine innovation.As a Compliance Manager, you will be at the forefront of ensuring the correct qualification and validation status of GMP critical equipment and processes. Additionally, you will take a leading role in implementing ...

Join a world leading pharmaceutical organization to create a safer and healthier world through vaccine innovation

As a Compliance Manager, you will be at the forefront of ensuring the correct qualification and validation status of GMP critical equipment and processes. Additionally, you will take a leading role in implementing comprehensive quality and safety programs within the department.

Take this opportunity to lead, inspire, and make a lasting impact on the organization.

Apply now and be part of a team that is shaping the future of healthcare


The Compliance Manager will lead a motivated and dynamic Engineering-Validation-Maintenance (EVM) department for a leading organisation in the pharmaceutical industry.

As part of the EVM team, you will provide technical support for utilities, production, and laboratory areas, ensuring high GMP and EHS (Environment, Health & Safety) standards.

Responsibilities:

  • Lead a team of engineers/technicians, promoting diversity, inclusion, and equity;
  • Ensure a stable team with a positive atmosphere through motivation, coaching, and support;
  • Set priorities aligned with departmental goals and optimize the efficiency of quality and safety processes;
  • Manage the life cycle of technical assets according to pharmaceutical regulations;
  • Implement and maintain safety aspects of the EHS (Environment, Health & Safety) program;
  • Maintain company quality standards and procedures;
  • Prepare for internal and external audits;
  • Drive departmental improvement using tools and goal setting;
  • Provide training to team members.

  • Bachelor's degree in engineering, biotechnology, automation, or equivalent;
  • Minimum 10 years of experience in biotechnology/pharmaceutical/process industry with people management;
  • Knowledge of pharmaceutical manufacturing, cGMP, and safety regulations;
  • Experience in validation and qualification of equipment, utilities, and facilities;
  • Strong leadership, communication, and collaboration skills;
  • Fluent in English;
  • Lean methodology experience preferred.

  • A salary range around €80K gross a year (based on education and working experience);
  • A full-time contract with flexible working hours;
  • An opportunity to be part of a global market leader;
  • A dynamic and inspiring working environment, including operating globally;
  • Opportunities to work on challenging projects and assignments;
  • Possibilities for further personal and professional development/education;
  • Excellent benefits.

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