Process Validation Engineer - Cleanroom

Are you a highly skilled Engineer who is dreaming of a job with a real impact on patients ’lives?

Do you want to work for an innovative specialist spinal implant company and play a crucial role in ensuring efficiency of our manufacturing processes?

                                                            If yes, come to join our Process Validation team

                                                                      (controlled cleanroom environment)

                                                   Together we can shape the future of the healthcare.

As Process Validation Engineer you will participate to the qualification-validation strategy for the processes and activities for which you are responsible (internally and externally).

You will work in close collaboration with R&D, Operations and RA departments and with sub-contractors to qualify their processes.

Your main responsibilities will be:

• As Clean Room/Water Loop and HVAC Subject Matter Expert (SME):

• Managing and monitoring cleanroom qualification activities, including environmental monitoring, requalification, and contamination control.
• Coordinating/executing validation activities (IQ/OQ/PQ) for equipment, utilities, and cleanroom systems.
• Leading investigations, root cause analysis, CAPA, and non-conformity resolution linked with clean room environment
• Ensuring compliance with ISO 13485, ISO 14971, 21 CFR Part 820, EU MDR 2017/745, and internal quality systems.
• Analysing quality metrics and identifying opportunities for continuous improvement.
• Creating, Reviewing and approving quality documentation, SOPs, protocols, and reports.
• Interacting with auditors
• Collaborating with Production, Engineering, Regulatory Affairs, and suppliers

• As a key contributor to the quality roadmap across the product development lifecycle:

• Participating to DHF completeness
• Defining, Planning , executing and reviewing all validation/verification activities 
• Managing all changes including impact assessment 

Your profile:

• Proven experience in Validation and Qualification processes in a Controlled manufacturing environment/ Iso-Classified cleanroom.
• Minimum of 3 years of experience in the medical devices or pharmaceutical
  industry with demonstrated use of ISO 13485, ISO 14971, 21 CFR Part 820, and EU MDR 2017/745
• Experience in orthopaedic and/or spinal medical device development is a strong advantage
• Higher qualification / degree as a Quality Engineer
• Ability to work effectively in English; native or near-native level of French
• Strong communication skills, with the ability to clearly convey technical information to diverse audiences and explain complex regulatory requirements in simple terms
• Excellent technical writing skills, including structured documentation such as protocols, reports, and audit-ready records
• Ability to manage multiple projects and validation activities under tight deadlines
• Ability to challenge decisions that may impact patient safety or regulatory compliance
• Strong problem-solving skills with a pragmatic and solution-oriented approach
• Valid driving licence