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CQV engineer Amsterdam QTC Recruitment

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Gevraagd

  • 40 uur
  • Medior/Senior
  • Engels (taal)

Aanbod

  • Vast contract
  • Bonusregeling, Doorgroeimogelijkheden
 

Vacature in het kort

Amsterdam
Our client, a pioneering biotechnology company, is seeking a CQV Engineer to enhance their facilities and technical operations. In this dynamic role, you'll lead commissioning, qualification, and validation activities, ensuring compliance with industry standards. Collaborate with cross-functional teams, mentor junior engineers, and drive continuous improvement. Enjoy a competitive compensation package, performance bonus, and opportunities for growth in a mission-driven environment. Uncover the reasons why this opportunity is worth considering.
 

Over het bedrijf

QTC Recruitment
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Bedrijfsprofiel
 

Volledige vacaturetekst

Our client is a leading biotechnology company dedicated to advancing life sciences through innovation and cutting-edge technology. Their solutions drive progress in research, development, and manufacturing, supporting breakthroughs across the industry. As the company continues to grow, they are expanding their team and are currently seeking a CQV Engineer to oversee and work on the facilities and technical operations. In this role, you will be responsible for ensuring the efficiency, safety, and scalability of their infrastructure, leading facility improvements, and optimizing engineering processes to support business growth.


This is how you will make the difference
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.

What you bring

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's in it for you
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.


 

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