Medical Device Quality Inspector - Day Shift (ISO 13485)
$43k - $46kRandstad USA
Randstad USA is seeking an on-site Quality Inspector to verify raw materials and finished devices using calipers, micrometers, and blueprints. The role requires 1–3 years of quality experience in regulated industries and strict adherence to FDA/ISO 13485 standards. You will work in a climate-controlled facility, with a salary of $43,000–$46,000 per year, first shift (8 AM–4 PM) and up to 6 hours overtime weekly. This position supports QA through logs, NCRs, and device history records. #J-18808-Ljbffr Randstad USA
Vacancy posted 7 hours ago
Similar jobs that could be interesting for youBased on the Medical Device Quality Inspector - Day Shift (ISO 13485) in Florida, NY vacancy
- Pall Aerospace is seeking a Quality Inspector II to verify and validate products, performing final... ...conformances and corrective actions under ISO 9001/AS9100. Onsite in New Port Richey,... ...and comprehensive benefits including medical/dental/vision, 401(k), and eligibility for...Day shift
$43k - $46k
...seeking an on‑site Quality Inspector to verify raw... ...materials and finished devices using calipers,... ...regulated industry (medical device, aerospace,... ...adherence to FDA/ISO 13485 standards. We offer... ...$46,000 per year Shift: First Work Hours... ...for thirty (30) days. #J-18808-Ljbffr...SuggestedShift work- ...the roleImagine starting your day by checking a calibrated... ...step. As a Junior Dimensional Quality Inspector, you’ll perform foundational... ...process assemblies, and finished devices to keep products aligned... ...Dimensioning & Tolerancing)ISO 13485 familiarityQuality control...SuggestedContract workWork at office
- Terumo Aortic is looking for a Quality Assurance Manager in Florida, NY. The successful... ...operation staff, ensuring compliance with ISO standards and managing nonconforming... ...Engineering, alongside significant experience in medical device processes. Applicants should exhibit...Suggested
- ...and other aerospace & defense applications. Our reputation for quality, service, and dependability has permitted us to serve many of the... ...& defense original equipment manufacturers. The Quality Inspector inspects parts, assemblies and finished products to drawings and...Day shiftWork at office
- ...GmbH is looking for a Packaging Supervisor to manage finished device production at their Ave Maria, FL location. The successful candidate... ...offers opportunities for professional development and working within a leading medical device company. #J-18808-Ljbffr Arthrex GmbHDay shift
$112k - $145k
...About This Role The Quality Control Manager leads Quality Control... ...Manufacturing Quality Inspectors and Receiving Inspection teams... ...Ensure QC operations comply with ISO 13485, QSMR/FDA 21 CFR 820 and... ...progressive experience in a medical device manufacturing environment, with...El Camino Health
Florida, NY2 days ago- ...sciences, bioprocessing, microparticles, medical device, specialty chemical and eChem... ...functional teams, including production, quality assurance, and planning. Reports OOS results... ...to ensure compliance with 820 GMP and ISO 13485 standards. Assists on the review and revision...Contract work
Polysciences
Florida, NY17 hours ago - Terumo Aortic is looking for a Quality Control Supervisor to oversee inspectors in the Quality Operations program... ...compliance with quality systems such as ISO 13485 and managing non-conformance... ...and have over five years in the medical device industry. A strong analytical...
- ..., and logistical support to the Quality Operations program. Supervises inspectors in Quality Control Operations Areas... ...such as, but not limited to, ISO 13485, 21 CFR Part 820, MDSAP, MDD (9... ...Engineering or more than 5 years in the Medical Device industry with more than 5 years...
- ...We're partnering with a growing medical device manufacturer seeking a Senior Quality Engineer to support an orthopedic product... ...design controls, risk management (ISO 14971), and V&V activities Support... ...of FDA 21 CFR Part 820, ISO 13485 & ISO 14971 Details: Available for...
FPC of Savannah
Florida, NY6 hours ago - Andritz AG is seeking a Quality Control Lead for its facility in Oldsmar, FL. This role involves overseeing all quality control activities, implementing quality standards, and ensuring products meet specifications. Candidates must possess a minimum of 5 years of experience...
- ...to support rapid growth and optimizing the P2P process in a medical device environment. Candidates should have 10+ years in procurement,... ...years in Medical Device/Pharma/Biotech, and familiarity with ISO 13485 and FDA regulations. Excellent leadership and negotiation skills...
- ...Senior Quality Engineer | Orthopedic Joint Implants | On-site, Florida... ...Shoulder) at an established medical device manufacturer. You will... ...product development, ensuring FDA, ISO, and design control... ...of FDA 21 CFR Part 820, ISO 13485, and global regulatory requirements...
Skills Alliance
Florida, NY6 hours ago - Skills Alliance is seeking a Senior Quality Manager focused on Orthopedic Medical Devices in New York. This leadership position will oversee the Quality Engineering function, ensuring compliance with FDA, ISO 13485, and maintaining audit readiness. The ideal candidate will...
- ...submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions and technical files for CE Marking... ...of FDA regulations and international standards (e.g., ISO 13485, MDSAP, EU MDR) Proficiency with Microsoft Office Suite Proficiency...Work at office
Jobtailor
Florida, NY2 days ago - ...partnered with an innovative neurovascular medical device start-up as we look to recruit a VP/Director of Regulatory and Quality Assurance in Florida. Our client is an early... ..., actionable plans. RAC, CQE, CQA, or ISO 13485 lead auditor experience. What’s on Offer...
- ...Sandvik has an opportunity for a Quality Assurance Inspector in Alachua, Florida USA (... ...to the IMS System (ISO 9001:2015, ISO 14001:2015 &... ...including:Health care coverage (medical, dental, vision, prescription... ..., telemedicine) starting 30 days after hire.Paid vacation with...Full timeWork at officeWorldwide
Sandvik
Florida, NY3 days ago - Senior Quality Manager | Orthopedic Medical Devices | Location: Gainesville, FL | Orthopedic Medical Devices A growing orthopedic medical device company... ...life-cycle. What you will own: Compliance with FDA, ISO 13485, MDSAP and EU MDR, maintaining audit readiness and certification...
- ...the maintenance and improvement of the quality systems. Develops quality standards and... ...minimum of five years of experience in medical device quality assurance. Experience with class... ...of quality system regulations (ISO 13485, 21CFR820) and working knowledge of Computerized...Immediate start
Terumo Aortic
Florida, NY6 hours ago - ...experienced, and highly-analytical Quality Control Inspector to join our production... ...techniques. Willing to work shift from Monday - Thursday 3:30... ...Control Dimensional Inspection ISO 9001:2015 Awareness... ...drug test within 2 business days of your offer acceptance and...Shift workAfternoon shift
JE Technology
Florida, NY2 days ago - ...CNC Manufacturer seeking experienced QC Inspector. The QC Inspector is responsible for inspecting... ...drawings and the parts meet customer's quality standards. The Quality Control Inspector... ...random inspections throughout the day. Immediately coordinate any problems with...Day shiftFull timeImmediate startFlexible hours
- ...CNC Manufacturer seeking experienced QC Inspector. The QC Inspector is responsible for inspection... ...drawings and the parts meet customer\'s quality standards. The Quality Control Inspector... ...random inspections throughout the day. Immediately coordinate any problems with...Day shiftFull timeImmediate startFlexible hours
- ...Responsible for supporting the quality operation staff in the... ...QA/QC staff, GMP and ISO compliance. Key... ...areas, including all inspectors, analysts, and... ...but not limited to, ISO 13485, 21 CFR Part 820, MDSAP... ...Sciences. Understanding of medical device design and process...
- Kelly is seeking an A&P Quality Inspector for a temp-to-hire position in Pembroke Pines, FL. The role requires 1st shift and involves inspections on helicopters and parts to ensure airworthiness and regulatory compliance. You will review FAA data against company standards...Day shiftTemporary workShift work
- ...regulatory requirements (FDA 21 CFR Part 820, ISO 13485, and applicable combination product... ...activities meet regulatory and quality expectations. Risk Management & Compliance... ...Experience 3-7+ years of experience in: Medical device, pharmaceutical, or combination product...
- ...design requirements. Perform data entry, problem solving, and other quality control activities as assigned by management. Essential Job... ...Processing First Article Inspections preferred Experience working in an ISO 9001/AS9100 certified manufacturing environment preferred...Work at office
- ...and environmental responsibilities. The Quality Inspector II verifies and validates that products... ...manufacturing environment compliant with ISO 9001 / AS 9100. Experience interpreting... ...package, including paid time off, medical/dental/vision insurance, and a 401 (k) plan...Permanent employmentWork at officeMonday to FridayFlexible hours
$19 - $27.5 per hour
Job Summary Under minimal supervision, the QC Inspector II oversees quality projects, ensures compliance with Medline SOPs, and maintains product integrity... ...Basic knowledge of quality regulations such as GMP, GDP, ISO, or 21CFR 820, 210‑211. Work Experience At least 2 years...Hourly payMinimum wageWork experience placementWork at officeLocal area- ...submissions to obtain and maintain regulatory approvals for medical devices, including 510(k) submissions and technical files for CE Marking... ...of FDA regulations and international standards (e.g., ISO 13485, MDSAP, EU MDR) Proficiency with Microsoft Office Suite Proficiency...Work at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Medical Device Quality Inspector - Day Shift (ISO 13485). Be the first to apply!
Related searches
- quality inspector Florida, NY
- quality assurance inspector Florida, NY
- quality receiving inspector Florida, NY
- quality control assistant Florida, NY
- quality control inspector Florida, NY
- quality operator Florida, NY
- quality assurance assistant Florida, NY
- quality assurance medical device Florida, NY
- entry level medical device sales Florida, NY
- medical device sales no experience Florida, NY