As a CQV Engineer, you will be responsible for commissioning, qualification, and validation activities, ensuring that equipment, systems, and processes meet regulatory and operational requirements. You’ll lead complex projects, ensuring compliance with industry standards and company objectives. Your role involves developing validation protocols, executing tests, analyzing data, and troubleshooting issues to optimize performance. You’ll collaborate with cross-functional teams, including quality assurance and engineering, to ensure seamless implementation of validated systems. You will also mentor junior engineers, promote best practices, and ensure adherence to compliance standards while contributing to the continuous improvement of validation processes.

You, as the ideal CQV engineer will recognise yourself in the following:

• Bachelor or Master degree in Engineering, Biotechnology, Life Sciences, Chemistry, or a related field;
• 3+ years of experience in commissioning, qualification, and validation within the biotechnology, pharmaceutical, or medical device industries;
• Experience with equipment qualification (IQ/OQ/PQ), process validation, and regulatory compliance (e.g., GMP, FDA, EMA);
• Excellent communication and collaboration skills.

What we offer: 

• Key role in shaping the future of the company;
• Competitive compensation package including a performance bonus;
• Strong Company Culture: You’ll be part of a supportive, mission-driven team where everyone is dedicated to improving healthcare through innovation and quality;
• Opportunities for Growth & Development;
• Cutting-Edge Tools & Resources.