QA & Regulatory Affairs Associate: Medical Devices
Imagingexcellencesymposium
Canfield Imaging Systems in Parsippany-Troy Hills, NJ, seeks a Quality Assurance and Regulatory Affairs Associate to support day-to-day QA activities and regulatory audits. You will assist global device registrations, maintain documentation, and contribute to training and administrative tasks with a focus on ISO 13485 compliance.
The role requires 3+ years' QA/regulatory experience, strong communication skills, and proficiency in MS Office.
#J-18808-Ljbffr- ...Imaging Systems in Parsippany, NJ is seeking a Quality Assurance: Quality Assurance and Regulatory Affairs Associate to support QA and regulatory activities in a fast-paced medical device environment. The role focuses on audits, regulatory registrations, documentation, and...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
$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- ...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
$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 glass—a...Medical deviceHourly payLocal areaDay shift$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- ...quality of life, enabling patients to have their life-saving medication on hand wherever and whenever needed We see our... ...Responsibilities Proficient understanding of medical device design controls and regulatory requirements per 21 CFR 820, ISO 13485:2016 and 21 CFR...Medical device
- ...Regulatory Affairs Specialist Job Type: Full time - Permanent Location: Madison, New Jersey (On-site) A commercial-stage transplant technology... ...discipline ~3+ years of regulatory affairs experience in medical devices or a similar industry ~ Working knowledge of FDA...Medical devicePermanent employmentFull timeRemote 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- ...seeking a highly organized, detail-oriented QA Documentation Supervisor (Mfg. & Pkg.)to... ...), Batch Packaging Records (BPRs), and associated documentation for completeness, accuracy... ...in a regulated pharmaceutical, medical device, or biotech environment. ~ Deep understanding...Medical device
- ...and ensure compliance with applicable regulatory and quality standards.Roles & Responsibilities... ..., Quality Management, Regulatory Affairs, Business Administration, or a related... ...Excellence, or a related function within the medical device industry.Experience developing,...Medical deviceWork at office
$127.28k - $190.92k
...Management System (QMS) in accordance with regulatory requirements and to ensure the adherence... ...proactive planning and completion for QA Agreements establishment and review... ...years in pharmaceutical, biological and/or medical device operations including first-hand knowledge...Medical deviceContract workFor contractorsLocal areaNight shift$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- ...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
- ...ABOUT ORGANOX: OrganOx is an innovative, fast-paced, global medical device company with a mission to save lives by making every... ...and regions. Position Summary The position of Senior Regulatory Affairs Specialist is responsible for preparing regulatory submissions...Medical deviceFor subcontractorRemote workFlexible hours
- ...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
- ...IQVIA LLC in Parsippany-Troy Hills, NJ is seeking an Associate Territory Representative to launch your medical device sales career. You will hunt outpatient urology/urogynecology clinics, educate clinical staff, and drive prescriptions with physicians and NPs. You...Medical device
- ...Our client is currently seeking a Medical Device Tooling ProgramsCheck you match the skill requirements for this role, as well as associated experience, then apply with your CV below.DegreedProject Execution from Start to finishTechnical expertise enough to work with...Medical device
- ...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
$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- ...Job TitleParticipate in a multidisciplinary technical team to develop regulatory strategies and solutions for a wide range of Crop Protection & Nutrition clientsProvide support for the preparation and submission of applications to US EPA for registration of pesticides...Local area
- ...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
- ...Embecta, a global medical device company with a century in insulin delivery, is hiring a Global Medical... ...markets. Reporting to the Global Head of Medical Affairs, you will lead safety governance, risk assessments, and regulatory submissions while collaborating with...Medical device
- ...architecture, integration, and life cycle direction of regulated medical device systems spanning hardware, firmware, and clinical use... ...domains, perform risk management per ISO 14971, and contribute to regulatory submissions while mentoring engineers and coordinating cross-...Medical device
- 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
- ...ensure R&D functions meet cGMP and company procedures. Responsibilities include documentation review, audits, study releases support, and regulatory guidance, with QA representation on project teams and ongoing training for personnel in Quality processes. #J-18808-Ljbffr...
- ...Preventative Maintenance OperatorOur client, a Medical Devices/Healthcare company, is looking for a Preventative Maintenance Operator for their Parsippany, NJ location. Responsibilities include organizing the Preventive Maintenance group, scheduling work, managing overtime...Medical device
- ...Job Description Job Description QA_(2024-10-29) Do you want to be part of an... ...from 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
$230k - $250k
...within the pharmaceutical, biotechnology, medical device, or healthcare industry. Minimum of... ...across Sales, Market Access, Medical Affairs, Marketing, and Operations within a matrix... ...business in accordance with all legal, regulatory, and company policies while...Medical deviceFull timePart timeLocal areaImmediate startWorldwide
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