MASY Group GmbH, a leading GMP Compliance firm specializing in Qualification, Validation (CQV), and Business Development, is seeking a dynamic and experienced professional to join our team. As we continue to expand our global presence, we are committed to attracting top-tier talent to contribute to our innovative projects across various industries, including pharmaceuticals, medical devices, and biotechnology.

As a Qualification and Validation Engineer at MASY Group GmbH, you will be an integral part of our mission to uphold industry standards and deliver excellence. This role offers a unique opportunity to work on cutting-edge projects, ensuring the compliance and validation of systems crucial to our clients' success. To include: 

• Execute Qualification and Validation processes in alignment with industry standards and client requirements.

• Collaborate with cross-functional teams to plan, implement, and oversee validation projects throughout their life cycle.

• Conduct risk assessments and contribute to the development of robust quality management systems.

• Stay abreast of industry regulations and technological advancements, integrating them into project strategies.

• Generate comprehensive documentation, including validation plans, protocols, and reports.

• You have a proven background in Qualification and Validation processes, preferably in pharmaceuticals, medical devices, or biotechnology.

• Your expertise includes executing validation protocols and ensuring compliance with industry regulations.

• You thrive in a collaborative environment, working seamlessly with cross-functional teams.

• Attention to detail and a commitment to excellence are ingrained in your work ethic.

• Strong communication skills enable you to convey complex concepts effectively.

MASY Group GmbH is an equal opportunity employer and values diversity in the workplace.

Qualification & Validation Engineer

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