QA & Regulatory Affairs Associate (Medical Devices)
Imagingexcellence
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 cross-functional teams. The ideal candidate holds a Bachelor's degree with 3+ years of QA/Regulatory experience, familiarity with ISO 13485 and GCP/ICH practices, and strong communication skills. #J-18808-Ljbffr
- Quality Assurance: Quality Assurance and Regulatory Affairs Associate The Quality Assurance and Regulatory... ...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 timeWork experience placementWork at office
- ...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
- ...I (BMET I)Required Skills & Experience: Associate's degree in Biomedical Equipment Technology... ...maintenance/repair. Understanding of medical equipment calibration, troubleshooting,... ...installations and inventory, and ensure medical devices remain safe and functional for patient...Medical deviceInternship
- ...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...Suggested
- ...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...Medical deviceWork experience placement
$60 per hour
...procedures by explaining examinations, reviewing medical histories, and ensuring patient comfort.... ...images. Operate MRI scanners and associated imaging equipment while maintaining... ...safety concerns, including implants, medical devices, and contraindications. Select...Medical deviceHourly payFull time$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- ...Hospital & Health Care Type Privately Held Founded 2022 Employees 1001-5000 Categories Manufacturing Medical Devices Medical Care Health Care MedTech Medical Supplies Healthcare Patient Management Research & Innovation Medicine...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$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€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- ...Demonstrated experience implementing SAP QM within a highly regulated manufacturing industry (such as Aerospace & Defense, Automotive, or Medical Devices) with strict traceability standards.Implementation History: Proven track record of participating in at least two full lifecycle...Medical deviceFull time
- ...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
- ...IQVIA is seeking an Associate Territory Representative to drive medical device sales in outpatient urology and urogynecology clinics across a defined territory. This entry point role emphasizes prospecting, relationship-building with physicians and clinic staff, and achieving...Medical device
- ...or an alternative application process. Regulatory Associate Clinical Operations SATX Full Time... ...conduct of clinical pharmaceutical and device protocols. The Regulatory Associate serves... ...ensure copies of all current and applicable medical licenses and training documentation are...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
- ...manufacturing quality activities while helping maintain strong audit and regulatory readiness. RESPONSIBILITIES Lead, coach, and develop Quality... .... Minimum 7 years of related quality experience within medical device manufacturing. Minimum 3 years of team leadership or...Medical deviceFull timeWork at office
- ...that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to... ...The Category Activation Medical Affairs Senior Associate plays a key role in translating scientific... ...types of products like Medical devices, Personal care products. The...Medical deviceTemporary workLocal areaVisa sponsorship
$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$19.95 per hour
...A Packaging Operator / Medical Device Production Associate position in Parsippany, NJ with Adecco US, Inc. focuses on operating packaging equipment, inspecting implants, and maintaining production records in a cleanroom environment. Responsibilities include passivation...Medical deviceHourly payDay shift- ...embecta, a global medical device company with a rich legacy and hybrid work in Parsippany, NJ, is seeking a Senior Internal Auditor. You will evaluate internal controls, lead audit workstreams, and collaborate with management and external auditors to maintain ICFR and...Medical device
- ...injuries, illnesses or disabilities. Monitors patients, administers medications, keeps records, consults with healthcare providers, educates... ...side effects and reactions. 3. Prescribes assistive medical devices and related treatments. 4. Monitors, reports, and records...Medical deviceDaily paid
- ...EGN Consulting & Talent Recruiting in Morristown, NJ seeks a Sales Engineer to build relationships for medical-device manufacturing equipment and packaging solutions. This role blends hunter and farmer activities, visits customers nationwide, and travels 20–30% primarily...Medical deviceRelocation
- ...Corp seeks a Senior Quality Engineer to ensure investigations, procedures, and activities comply with FDA QSR, ISO 13485, and Medical Device Directives for Vigilance. You will review customer complaint investigations for validity and ensure they are processed per corporate...Medical deviceRemote work
- ...actions, and verify effectiveness to ensure design quality and regulatory compliance. The role operates with autonomy as a technical... ...and regulatory expectations, while collaborating with Quality, Regulatory Affairs, and Manufacturing Engineering. #J-18808-LjbffrMedical device
- 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
- Getinge in Wayne, NJ is seeking a production team lead to oversee workflow and assist the supervisor in meeting daily production schedules and quality goals. You will train staff, schedule workflow, and help introduce new processes to improve efficiency. The role emphasizes...Medical device
- ...products, processes, and documentation comply with applicable regulatory requirements, internal procedures, and quality standards.... ...preferredExperience0–3 years of experience in a regulated environment (medical device preferred)Experience with ISO 13485 or FDA regulations is a...Medical deviceWork at office
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