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Multi-Disciplinary Engineers Breda SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • Medior/Senior
  • Engels (taal)

Aanbod

  • Vast contract
 

Vacature in het kort

Breda
Join an innovative organization dedicated to advancing science and technology to improve lives. Be a part of a team that develops treatments for serious diseases and addresses unmet medical needs. Opportunities are available for engineers specializing in automation, electrical, validation, maintenance, mechatronics, and CQV. Enjoy a competitive salary, career growth, and the chance to work on impactful health projects in a cutting-edge pharmaceutical environment. Continue reading to find out why this challenge is waiting for you.
 

Over het bedrijf

SIRE Life Sciences
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The Company
Our client is an innovative organization dedicated to advancing science and technology to improve lives. By leveraging cutting-edge research, they develop treatments for serious diseases and continuously expand their pipeline to address unmet medical needs.

We’re currently looking for: 

  • Automation Engineers

  • Electrical Engineers

  • Validation Engineers

  • Maintenance Engineers

  • Senior Mechatronics Engineers

  • CQV Engineers (Commissioning, Qualification & Validation)
     

Key Responsibilities (Role-Dependent)
  • Conduct Commissioning, Qualification & Validation (CQV) activities for equipment, utilities, and facilities.

  • Lead and support Computerized System Validation (CSV) to ensure GMP and FDA compliance.

  • Develop and execute validation protocols (FAT, SAT, SIT, IQ, OQ, PQ).

  • Support automation systems from design to lifecycle management.

  • Troubleshoot and maintain secondary packaging systems, including print and inspection technologies (e.g., Systech, Cognex).

  • Apply project management skills for CAPEX projects, focusing on timelines, budgets, and compliance.

  • Provide hands-on support for secondary packaging operations.

  • Utilize mechatronics and analytical troubleshooting to resolve equipment issues.

Requirement
  • Bachelor's or Master’s degree in Engineering, Science, or a related technical field (or equivalent experience).

  • 5+ years of relevant work experience, including 4 years in an operations/manufacturing environment.

  • Strong knowledge of GMP, OSHA, EPA standards, and regulated environments.

  • Fluent in English (spoken and written); basic Dutch is a plus.

  • Flexibility to occasionally work outside regular hours.

  • Excellent communication, stakeholder management, and problem-solving skills.


Why Join Us?

  • Work in a cutting-edge pharmaceutical manufacturing environment.

  • Collaborate with a multidisciplinary team on impactful health projects.

  • Competitive salary and benefits package with opportunities for career growth, training, and international exposure.

  • Contribute to innovative medicine and improving lives.

Other Information
If you are ready to make a global impact in the Healthcare industry, apply to this vacancy now!
Look forward to chatting with you!
 

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