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- Elos Medtech AB in Rosenheim sucht einen Mitarbeiter Qualitätsmanagement (m/w/d) in Vollzeit ab sofort für eine befristete Anstellung. Ihre Aufgaben umfassen die Pflege des Qualitätsmanagementsystems, die Einhaltung regulatorischer Anforderungen und Unterstützung bei Audits...Suggested
- ATL Corp is seeking a Quality Manager to lead the Quality Management System and ensure compliance with ISO 13485 and customer specifications. This role drives quality improvement initiatives, oversees quality assurance activities, and provides technical leadership across...Suggested
- Intertech Medical LLC is looking for a Validation Inspector in Denver, Colorado. This critical role involves performing detailed measurements and inspections to ensure product quality. You will work closely with the Quality and Engineering teams to maintain compliance with...Suggested
- Balda-C-Brewer is seeking an Engineering and Program Management professional in New York, NY. Responsibilities include project launch and integration, customer relationship management, and improving operational efficiencies in the manufacturing process. The ideal candidate...Suggested
- Overview Freelance FDA Consultant (ISO 13485 & ISO 22716 Experience) USA Remote (with occasional on-site client visits) Contract / Self-Employed Basis About IMSM IMSM (International Management Systems Marketing) is a global force in ISO consultancy -helping organisations...SuggestedContract workFor contractorsSelf employmentFreelanceRemote workWorldwideFlexible hours
- ...manage operations and staff. Responsibilities include overseeing procurement, manufacturing scheduling, and ensuring compliance with ISO 13485 and FDA regulatory standards. The ideal candidate must possess a Bachelor’s degree and at least 4-5 years of managerial...Suggested
- A leading contract manufacturer based in Mequon, WI is seeking a Quality Specialist to ensure compliance with quality standards for electro-mechanical subassemblies. This role will support supplier audits, maintain quality systems, and drive continuous improvement initiatives...SuggestedContract work
$110k - $140k
A manufacturing company is seeking a Quality Manager to lead quality processes and systems, ensuring compliance with ISO standards. The candidate will oversee the Quality Management System, manage customer complaints and audits, and foster continuous improvement initiatives...SuggestedFull time- ...Quality and Compliance Auditor in Mount Pleasant. The role involves auditing the Quality Management System (QMS) to ensure compliance with ISO standards and supporting a high-precision contract manufacturing environment. The ideal candidate holds a related Bachelor’s degree...SuggestedContract work
- ...tsmanagement übernimmt und das bestehende QM-Team leitet. Sie werden aktiv an der Weiterentwicklung des Systems nach ISO 9001 arbeiten und die Umsetzung der ISO 13485 unterstützen. Eine reflektierte Persönlichkeit mit mehreren Jahren Erfahrung im Qualitätsmanagement sowie...SuggestedFlexible hours
- ...ensure compliance with quality standards. The role involves managing QA operations, implementing policies, and ensuring adherence to ISO 13485:2016 standards. The ideal candidate has a Bachelor's Degree in a relevant discipline, 3-5 years of managerial experience, and...Suggested
- Intertech Plastics LLC is seeking a D Shift Quality Inspector to perform visual and dimensional inspections on manufactured parts, document non-conformances, and support QA processes. The role operates on-site in Denver, CO with shift schedule matching the production cycle...SuggestedHourly payFull timeShift workAfternoon shift
- Viant Medical is seeking a QA Technician in San Antonio, Texas to support quality system activities ensuring compliance with ISO 13485 and company procedures. The role involves performing inspections, testing, and documentation reviews, along with assisting in quality...SuggestedWork at office
- G&F Precision is seeking a dedicated Quality Auditor in Danvers, MA to evaluate processes, systems, and products for compliance with standards, regulatory requirements, and internal policies. Responsibilities include directing operations with production, aligning quality...Suggested
- ...documentation, shaping a culture of quality and accountability. The ideal candidate has 5+ years in quality within regulated manufacturing, expertise with AS9100, ISO 13485, and FDA QSR, and experience guiding cross-functional teams to audit #J-18808-Ljbffr Arrow StaffingSuggested
- ...customer quality, calibration, and team development, building a culture of quality and accountability. The role requires 5+ years in medical device quality, AS9100, ISO 13485, and leadership of quality teams; Bachelor's degree preferred. #J-18808-Ljbffr Arrow Staffing
- ...Inc. is seeking a Quality Manager in Menomonee Falls, WI. This role is critical for leading the Quality Management System to meet ISO 13485 standards and ensure product compliance. The successful candidate will oversee quality assurance, drive continuous improvements,...
- ...II at our Detroit, Michigan facility. This role focuses on supporting product release activities and maintaining compliance with ISO 13485 standards. Qualified candidates must hold a Bachelor’s Degree in a scientific field and have at least 2 years of experience in a...
- ...seeking a Quality Inspector II in Big Lake, MN. The successful candidate will oversee quality control functions, ensuring adherence to ISO 13485 standards and performing inspections on machined components. The position requires a minimum of 3-5 years of experience in a...
- X4 Life Sciences is seeking an Operations Quality Manager to oversee manufacturing-related quality activities. This role involves ensuring products are built safely and consistently with compliance to internal and regulatory standards. The ideal candidate has over 6 years...
- ...activities to ensure regulatory compliance. The role collaborates with manufacturing, engineering, and quality teams to drive continuous improvement and timely corrective actions. A background in medical devices and ISO 13485 is preferred. #J-18808-Ljbffr Catalyst MedTech
- IMSM is seeking a Freelance FDA Consultant with expertise in ISO 13485 and ISO 22716. This role involves providing strategic guidance on FDA regulatory requirements, supporting submissions and inspections, and developing Quality Management Systems (QMS). Ideal candidates...Remote jobFreelance
- Vonco Products, LLC is seeking a Quality Assurance Technician I to support product quality in production and testing areas. You will perform tests, verify setups, and communicate non-conformances to initiate corrective actions, ensuring compliance with company requirements...
- Actalent is seeking a Quality Assurance Specialist II in Bedford, MA to support cGMP, FDA, and ISO 13485 compliance within a regulated manufacturing setting. The role involves reviewing batch records, guiding deviation investigations, and ensuring robust quality documentation...
- ...Dental Products seeks a Quality Systems Manager to maintain the Quality Management System and oversee QA/QC activities in support of ISO 13485 and medical device regulatory requirements. This hands-on leadership role involves managing quality system processes, QA/QC...
- ...customer quality, and team development to build a culture of quality and accountability. The ideal candidate has 5+ years in medical device quality, strong knowledge of ISO 13485 and FDA QSR, AS9100, and experience mentoring quality teams. #J-18808-Ljbffr Arrow Staffing
- ...quality standards. The ideal candidate will oversee the Quality Management System, manage daily operations, and ensure adherence to ISO 13485:2016 and regulatory requirements. Applicants should have a Bachelor’s Degree in a relevant field and significant managerial...
- ...operations manager responsible for overseeing daily operations, recruiting and training staff, and ensuring all processes comply with ISO 13485 and FDA regulations. The role requires developing KPIs to monitor performance and collaborating with the finance team to maintain...
- ...Rand is seeking a Site Quality Lead to join their Chicago team. This role is responsible for ensuring product quality, compliance with ISO standards, and effective management of the Quality Management System. You will lead quality initiatives and partner across various...
$71k - $94.5k
Revvity is seeking a passionate Quality Specialist in Hopkinton, MA. This role involves driving documentation and support for our ISO 13485 Quality Management System. Responsibilities include managing QMS training, coordinating Change Orders, and tracking corrective actions...