QA & Regulatory Affairs Associate - Medical Devices
Sculptmydream
Canfield Imaging Systems in New Jersey seeks a Quality Assurance and Regulatory Affairs Associate to support audits, registrations, and documentation for medical devices. You will help maintain QA processes, ensure training documentation is complete, and assist with global regulatory submissions. The role requires a Bachelor’s degree with 3+ years in QA/regulatory roles, ISO 13485 exposure, and strong communication. Canfield offers comprehensive benefits and a path to professional growth. #J-18808-Ljbffr Sculptmydream
- The Quality Assurance and Regulatory Affairs Lead is responsible for assisting the Quality Assurance... ....Job Description:Support and act as a QA contact for regulatory and... ...audits, support and facilitate global medical device registrations with oversight from Senior...Medical deviceFull timeImmediate start
- Canfield Imaging Systems, Parsippany, NJ, seeks a Quality Assurance and Regulatory Affairs Associate to support QA activities, audits, and regulatory submissions for medical devices. The role emphasizes documentation control, training administration, and collaboration with...Medical device
- ...Parsippany, NJ, is seeking a Quality Assurance and Regulatory Affairs Associate to support day‑to‑day QA activities and global certification efforts. You... ...process improvements, and help prepare regulatory submissions for medical devices. #J-18808-Ljbffr CanfieldresearchgroupMedical device
- Canfield Imaging Systems in Parsippany, NJ seeks a Quality Assurance and Regulatory Affairs Associate to support QA activities, audits, and documentation in a fast-paced medical device setting. You will help maintain ISO 13485 compliance, assist with regulatory filings...Medical device
$16 per hour
...staffing agency in Denville, New Jersey, is seeking individuals for a Temp-to-Hire position involving the assembly and packing of medical products. Responsibilities include assembling products to specifications, packing and labeling finished goods, and maintaining a clean...Medical deviceHourly payTemporary workMonday to FridayDay shift- ...demands of patient safety, regulatory compliance, and an... ...yield variability, QA release buffers, and CMO... ...integrate commercial, medical affairs, regulatory, quality,... ...industries: Biopharma, Medical Devices / Med Tech, CDMO/CMO,... ...work experience. (If associate degree, must have a...Medical deviceWork experience placementLive inWork at officeLocal area
- ...initiatives, trends in work levels, and changing quality and regulatory needs.Foster collaboration and team work to create and share... ...design and/or manufacturing experience desired, experience in medical device industry highly desired.Professional certification from the American...Medical deviceWork experience placement
- ...Inc. in Florham Park, NJ, seeks an engineer to support electrical and manufacturing activities for medical device products, including design, documentation, and regulatory compliance. You will assist in V&V testing, develop schematics, PC board layouts, manuals and test...Medical device
$131.9k - $165k
...meaningful difference in people's lives. Our medical devices, software and related services are... ...level risk management activities associated with assigned programs.Under auspices... ...reliability, manufacturability/serviceability, regulatory and business objectives.Leads efforts...Medical deviceMinimum wageOngoing contractFull timeH1bLocal areaRemote workWorldwide$90k - $120k
...Engineer Salary: $90,000 - $120,000 Engineering Firm, On-site Location: Morristown, NJ ELECTROMECHANICAL/AEROSPACE/MEDICAL DEVICE MANUFACTURING Manufacturer of mechanical and electromechanical components needs someone to develop and improve manufacturing...Medical device- OrganOx in Madison, NJ is looking for an Intake Specialist to manage medical device complaint activities. This role involves communication between internal teams and customers to ensure compliance with complaint reporting processes. Candidates should have a Bachelor's...Medical device
- ...Recruiter | Insight Global | Pennsylvania State University Alumni Regulatory Site Quality Specialist JOB DESCRIPTION A large CPG client of... ...project teams and departments, and serving as a backup for the QA Manager. REQUIRED SKILLS AND EXPERIENCE BS degree in science or...
$150k
...Proven capability with Microsoft Office applications (PowerPoint, Excel, Word, etc.)Prior sales management experience preferred.Medical device B2B industry experience strongly preferred.Annual base salary range: $150,000 + $65,000 commission range at plan (uncapped over...Medical deviceTemporary workWork at office$22 - $25 per hour
...market position, producing specialized component parts for the medical device and telecommunications industries. This isn't your average... ...an unbeatable work-life balance! Plus, as a PrideStaff associate, you gain access to a comprehensive benefits package, including...Medical deviceHourly payTemporary workLocal areaWeekend workDay shift3 days per week- ...Regulatory Affairs Specialist Job Type: Full time - Permanent Location: Madison, New Jersey (On-site) A commercial-stage transplant... ...~3+ years of regulatory affairs experience in medical devices or a similar industry ~ Working knowledge of FDA regulatory...Medical devicePermanent employmentFull time
- ...maintenance, installation, troubleshooting of medical equipment used throughout hospital and... ...installations and inventory, and ensure medical devices remain safe and functional for patient care. Must-Haves: Associate’s degree in Biomedical Equipment Technology (...Medical deviceContract workInternshipShift work
$22 - $25 per hour
...highly respected manufacturing client. This company holds a strong market position, producing specialized component parts for the medical device and telecommunications industries. This isn't your average assembly line job. You will be working with technical glassa...Medical deviceHourly payLocal areaDay shift$86.25k - $124.58k
...people and need leaders and experts ready to shape what’s next. As a QA Compliance Specialist, you’ll bring your skill, your curiosity... ...cross-functional stakeholders to ensure timely investigations, regulatory compliance, and continuous improvement of quality systems and...Work at officeWorldwide$250k - $350k
embecta is a global medical device company with a 100-year legacy in insulin delivery and diabetes care. Driven by innovation, purpose, and... ...Operations, Legal, Compliance, Customer Service, and Medical Affairs to ensure successful execution of customer commitments....Medical deviceFull timeContract work€30k - €35k per year
...cost-effective, and user-friendly medical technologies that heal... ...looking for a Junior International Regulatory Specialist to join our Regulatory Affairs team, based in Bussolengo (Verona... ...position preferably in a Medical Device CompanyGood English and Italian,...Medical deviceContract work- ...Sterilization Services, LLC is a contract steam and dry heat sterilization provider serving the pharmaceutical, compound pharmacy, medical device, and biotech industries. Company Description Prince Sterilization Services, LLC is a contract steam and dry heat...Medical deviceFull timeContract workLocal areaMonday to FridayShift work
- ...manufacturing quality activities while helping maintain strong audit and regulatory readiness. RESPONSIBILITIES Lead, coach, and develop... .... Minimum 7 years of related quality experience within medical device manufacturing. Minimum 3 years of team leadership or...Medical deviceFull timeWork at office
- ...countries and regions. Position Summary The Regulatory Affairs Specialist supports global regulatory... ...and Notified Body interactions associated with assigned submissions and... ...Skills & Experience Working knowledge of medical device regulatory requirements and FDA regulatory...Medical deviceWork at officeFlexible hours2 days per week
- ABOUT ORGANOX: OrganOx is an innovative, fast-paced, global medical device company with a mission to save lives by making every... ...countries and regions. Position Summary The position of Senior Regulatory Affairs Specialist is responsible for preparing regulatory submissions...Medical deviceFor subcontractorRemote workFlexible hours
- ...Description Manager, Manufacturing Quality / Quality Manager, Medical Device Manufacturing Parsippany and Budd Lake, NJ (hybrid) ·... ...audits Keep the site ready for customer, certification, and regulatory inspections About you Be able to do the job as described...Medical deviceFull time
$19.96 per hour
Join the team at Adecco and become a vital part of the medical device manufacturing industry in Parsippany, NJ! We are seeking dedicated and detail-oriented Manufacturing Packagers / Production Associates to help produce high-quality medical products in a fast-paced, regulated...Medical deviceHourly payPermanent employmentTemporary workLocal areaImmediate startMonday to FridayShift work$180k
...Treasury for a Fortune companyExperience in capital markets, risk management, financing and capital deployment development and execution Additional Information$180K plus bonusSummaryType: Full-timeFunction: Accounting/AuditingExperience level: DirectorIndustry: Medical DeviceMedical deviceOverseas- ...on W2 Shift Timing: 8AM - 4PM ESTEssential Functions: Enforce regulatory compliance and quality assurance Prepare and maintain reports... ...Schedule, and on occasion attend and take minutes for site based medical staff department meetings Process and collect dues for the...Contract workShift work
- Getinge in Wayne, NJ, is seeking a manufacturing associate to build products following established processes and quality standards.... ...a high school diploma or equivalent and up to 12 months in a medical device manufacturing setting. Training on SAP basics and Lean principles...Medical deviceDay shift
- Job DescriptionJob Description QA_(2024-10-29) Do you want to be part of an organization... ...you! Our compliance with applicable regulatory guidelines and requirements is critical... ...assisting pharmaceutical, biotechnology and medical device companies with their drug development...Medical devicePermanent employmentTemporary workFor contractorsH1bWork at officeLocal areaWorldwideVisa sponsorship
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