Senior Quality Leader | ISO 13485 Medical Devices
Vonco Products, LLC
Vonco Products, LLC is seeking a hands-on Quality Manager to lead and continuously improve our ISO 13485 Quality Management System while supporting a fast-paced medical device packaging manufacturing operation. The role partners with Operations, Engineering, Supply Chain, and Customer Service to ensure compliance and drive continuous improvement. The ideal candidate will balance strategic quality system oversight with day-to-day operational support, lead CAPA activities, and effectively #J-18808-Ljbffr Vonco Products, LLC
- Vonco Products, LLC is seeking a Quality Manager to lead the ISO 13485 quality system and ensure compliance with regulatory and customer requirements in a medical device environment. This role partners with Operations, Engineering, Supply Chain, and Customer Service to...QualityMedical device
- Quality Manager | ISO 13485 Medical Device Manufacturing We are seeking a hands-on Quality Manager who can lead and continuously improve our ISO 13485 Quality... .... This individual will serve as the site quality leader, partnering closely with Operations, Engineering, Supply...QualityMedical device
- ARCH is seeking a Quality System Management Representative for the Elmhurst, IL and Kenosha, WI facilities to promote regulatory and quality... ..., developing metrics, and coordinating risk assessments and validation programs under FDA QSR 820 and ISO 13485. #J-18808-Ljbffr ARCHQualityMedical device
- ...Quality Leader At DuPont, we are working on things that matter, whether... ...in everyday technology devices from smartphones to electric... ...customer, regulatory, food-safety, medical-packaging, and DuPont quality... ...Management System; sustains ISO 9001, FSSC 22000, and applicable...QualityMedical deviceFlexible hours
- Senior Systems Engineer Location: North Plymouth MN... ...verification, and validation of medical devices. Responsibilities... ..., human factors, quality, manufacturing,... ...Drive adherence to FDA, ISO and IEC design control... ...collaboration with project leaders Creative problem...QualitySeniorMedical deviceContract workShift work
- ...EXALTA Group in Wisconsin (Kenosha) seeks a senior quality auditor to ensure compliance with FDA QSR and ISO 13485, lead internal and supplier audits, and drive... ...manufacturing. The role requires 5+ years of medical device QA experience, strong documentation control, and...QualityMedical device
- ...Purpose and Function: Independently perform quality-related functions within the Quality... ...combination of education and experience in medical device manufacturing · Proficient in applicable regulations/standards (ISO 13485, FDA, etc.) · Ability to read, analyze,...QualityMedical deviceFlexible hours
- ...efficient shift execution in a medical sterile packaging (converting... ...production activities meet quality, regulatory, and safety requirements... .... Ensure compliance with ISO 13485, ISO 11607, and internal... ...preferably in a cleanroom or medical device manufacturing environment....QualityMedical deviceWork at officeShift work
- ...required the person to have Knowledge with FDA regulations for Medical Devices, and ISO 13485 Medical Device-QMS-Requirements for Regulatory Purposes... ...activities, detection of problem areas, and delivering quality inspection outcomes. In addition, they are in charge of planning...QualityMedical deviceWork at office
- Uline, a leading distributor, seeks a Senior Human Resources Analyst in Pleasant Prairie, WI to drive analytics... ..., SQL, Workday and Power BI, partner with HR and leaders, and lead analytics projects to improve data quality and processes. A strong background in HR analytics...QualitySenior
- Winland Foods in Kenosha, WI is seeking a Quality Manager to lead FS&Q activities at the site level, oversee sanitation, and ensure compliance with regulatory and company policies. The role involves directing FS&Q team members, maintaining GFSI certification readiness,...QualitySenior
- ...Quality Engineers R&L Spring Company and Medicoil are both seeking Quality Engineers... ...Assist in maintaining compliance with ISO 13485:2016, ISO 9001, and/or IATF 16949 requirements... ...environment Experience with medical device and/or automotive quality systems preferred...QualityMedical deviceWork at office
- ...Description: Integration (Process Validation) Engineer Medical Device Contract Manufacturer – Flexible Films & Packaging... ..., and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements, and internal quality standards...QualityMedical deviceContract workFlexible hours
- Acts as a Quality System Management Representative for the Elmhurst (IL) and Kenosha (WI)... ...all applicable regulatory requirements for medical devices such as FDA Quality System Regulation - 21 CFR 820, GMP guidelines, GDP, ISO 13485, ISO and other applicable regulatory...QualityMedical device
$85k - $100k
A recruitment firm is looking for a Quality Control Specialist in Pleasant Prairie, Wisconsin. The ideal candidate will have over 5 years of quality experience in the medical device industry, with a strong understanding of ISO13485 and FDA standards. Responsibilities include...QualityMedical device- ...Differential Join EXALTA Group and help ensure the quality of high-precision components used in the medical device industry. We're looking for a detail-oriented... ...Ensure all records and documentation comply with ISO 13485, FDA, and company quality requirements Meet...QualityMedical deviceRelocation packageMonday to FridayShift workAfternoon shift
$90k - $110k
...specifications, geometry dimensions and quality standards including... ...other organizational key leaders/departments to achieve cohesive... .... Proven track record in medical device design and development.... ...ASME Y14.5M. Knowledge of ISO 13485 Quality Management System &...QualityMedical device$25 - $30 per hour
...4 hours Benefits Competitive salary Health insurance Opportunity for advancement Paid time off Training & development Project Team Leader Perks Aggressive Competitive Wages Health Insurance Paid Time Off Sick Pay Paid Training for Career Advancement Online Mobile Courses...QualityHourly payWork at officeImmediate startFlexible hours$32 - $34 per hour
...the Director of Wellness to supervise the nursing staff, ensuring residents receive high-quality, compassionate care. Ideal candidates are RN-licensed with a strong love for seniors, capable of staying calm and professional, and eager to contribute to a supportive team...QualitySeniorHourly payPart timeWeekend work- PuroClean is seeking a Project Team Leader to manage and complete jobs following our established processes. You will respond to service... ..., supervise production work, and ensure safety and quality from start to finish. With a focus on customer satisfaction, you...QualityFlexible hours
- PuroClean of Burlington is seeking a Project Team Leader to manage and complete jobs per PuroClean processes while responding to service calls as needed. You will set up efficient job flow, coordinate requirements, complete documentation, supervise production work, and...Quality
- ...significant improvements in safety, quality, delivery and cost by... ...that the business complies with ISO, FDA, EPA, OSHA and all other... ...experience Experience in Medical Device manufacturing and machining environment... ...a high sense of urgency Seniority level Seniority level...QualityMedical deviceFull time
$25 - $30 per hour
...repairs, and final acceptance testing on medical devices, including but not limited to cleaning,... ...high volume production setting adhering to ISO and FDA Regulations. Qualifications... ...organization adhering to ISO, FDA, or comparable quality systems and regulations. Ability to read...QualityMedical deviceShift work- Experience Burlington is seeking an experienced leader for commercial construction projects in Burlington, Wisconsin. The role involves... ...activities, and managing specialty trade contractors to ensure quality construction. The ideal candidate will have a Construction...QualitySeniorFor contractorsAfternoon shift
- ...seeking a QA Specialist for a 12-month onsite contract in Pomona, CA. The ideal candidate will have experience in quality assurance within the medical device field, ensuring compliance with manufacturing standards. Responsibilities include reviewing batch records,...QualityMedical deviceWeekly payContract work
$90k - $110k
...Wisconsin, is looking for a dedicated individual to lead the medical device design and production management. The ideal candidate will have... ..., emphasizing timely project completion and adherence to quality standards. This role involves collaborating with cross-functional...QualityMedical device- DuPont PPC, located in the Greater Chicago/Milwaukee region, seeks a PPC Quality Leader to oversee the site Quality function. You will own the Quality Management System, ensure ISO 9001 and FSSC 22000 compliance, and partner with Operations, Engineering, and Supply Chain...Quality
- ...customers across the medical device, automotive, powersports... ...alongside experienced leaders in a collaborative and... ...commitment to safety, quality, continuous... ...position serves as a senior advisor to the executive... ...OSHA reporting, ACA, ISO requirements, and related...QualityMedical deviceHourly payWork at officeShift work
$23 per hour
...Senior Medical Device Technician Position facilitates day-to-day operation of a medical device testing laboratory (BP monitors, TENS units, and nebulizers) responding to consumer complaints. There is no direct interaction with customers. Duties include transporting...SeniorMedical deviceWork experience placementWork at office- ...Job Title: QA Specialist (Medical Device) Location: Pomona, CA Mode: 100% Onsite / 12 Months Contract Pay Range: $20 to $25/hr on W2 Job Details Working knowledge of Quality Assurance in a medical device manufacturing environment, preferably in‑vitro diagnostic. Support...QualityMedical deviceWeekly payContract workTemporary workFlexible hours
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