Save Job Back to Search Job Description Summary Similar Jobs Added 09/07/2026ISO 13485 requiredStartup environmentAbout Our ClientOur client is an innovative medical technology company focused on developing advanced healthcare solutions that improve patients' quality of life. Operating in a highly regulated environment, the company combines scientific excellence, operational rigor, and a culture of collaboration and continuous improvement.Job DescriptionReview and approve manufacturing batch records while ensuring adherence to quality and regulatory requirements.Support incoming inspection activities, including review of certificates, inspection reports, and material documentation.Participate in non-conformance investigations, root cause analysis, and CAPA implementation.Support equipment qualification and process validation activities (IQ/OQ/PQ) at supplier and manufacturing sites.Ensure quality compliance throughout the product lifecycle in collaboration with external suppliers and manufacturing partners.Contribute to product release activities through quality record reviews and verification of test results.Collaborate closely with Regulatory Affairs, Procurement, Manufacturing, and Quality teams.Participate in supplier audits, readiness assessments, and continuous improvement initiatives.Maintain compliance with ISO 13485, FDA requirements, MDR, and internal quality management systems.The Successful ApplicantBachelor or Master's degree in Engineering, Life Sciences, or a related technical field.3-5 years of experience in Quality Operations within the medical device or another regulated industry.Knowledge of ISO 13485, FDA Quality System Regulations, and GxP requirements.Experience working with suppliers and contract manufacturing organizations.Familiarity with NC, CAPA, batch record review, validation activities, and risk management methodologies.Strong analytical, communication, and problem-solving skills.Experience with electronic quality management systems is considered an asset.What's on OfferOpportunity to join a growing and innovativeMedTechorganization.Exposure to a broad range of Quality Operations activities and international stakeholders.A collaborative environment focused on innovation, quality, and continuous improvement.Competitive compensation package and strong career development opportunities.Quote job refJN-072026-7059392Job summaryJob FunctionEngineering & ManufacturingSpecialisationQualityIndustryHealthcare / PharmaceuticalLocationVaudContract TypePermanentJob ReferenceJN-072026-7059392