Hybrid Medical Device Complaints Specialist (Regulatory MDR)
$37.18 per hourMillenniumSoft Inc
MillenniumSoft Inc is looking for a Complaint Management Specialist (Contract) in San Diego, California. The role requires 1-2 years of Quality, Regulatory, or Complaint management experience, particularly with medical devices, along with relevant qualifications such as a Bachelor’s degree in a scientific field. You will work on complaint management, ensuring regulatory compliance with FDA standards, and handling eMDR reports. The position offers a hybrid work setting with required local presence. Salary is $37.18 per hour. #J-18808-Ljbffr MillenniumSoft Inc
- ...Title: Specialist - Clinical Customer Advocacy Location:... ...including communication for regulatory compliance with medical device reporting for both... ...product event status and MDR reportability • Assures... ...to the review of events/complaints for Client products • Write...RegulatoryComplaintsMedical deviceContract workWork experience placementDay shift
- ...Title: QA Complaint Intake Specialist / Associate Location: San Diego, CA... ...follow-up, and verification of medical device complaints associated with... ...evaluation Potential regulatory reporting considerations... ...regulations, ISO 13485, EU MDR, and applicable regulatory...RegulatoryComplaintsMedical deviceWork at office
- ...Complaint Compliance Specialist (Specialist 3) Be part of something bigger... ...the largest global medical technology companies... ...complaints conform to regulatory requirements and... ...International Medical Device Regulators Forum (IMDRF) coding, EU MDR Vigilance, and other...RegulatoryComplaintsMedical deviceWorldwide
$90k - $115k
...experienced Veeva Vault EQMS Specialist with deep expertise in... ...Control, Deviations, CAPA, Complaints, Training). Facilitate workshops... ...quality standards, regulatory expectations, and IT/CSV methodologies... ...(Pharma, Biotech, or Medical Devices). ~ Hands-on experience...RegulatoryComplaintsMedical deviceMonday to Friday- ...Position : Sr. Complaint Specialist Investigation Lab/Post Market - Onsite Location : San Diego... .../week : 40.00 1st Shift Client : Medical Devices Company Job Category : Clinical... ...for complaint file documentation and regulatory reporting decision activities. Ensure...RegulatoryComplaintsMedical deviceContract workDay shift
- ...Position : Complaint Management Specialist Location : San Diego, CA Duration : 12 Months Total... ...week : 40.00 1st Shift Client: Medical Device Company Job Category: Healthcare... ..., including communication for regulatory compliance with medical device reporting...RegulatoryComplaintsMedical deviceContract workWork experience placementDay shift
- ...Position : Complaint Management Specialist Location : San Diego, CA Duration : 4 Months Total... ...week : 40.00 1st Shift Client : Medical Devices Company Job Category : Clinical... ...for complaint file documentation and regulatory reporting decision activities....RegulatoryComplaintsMedical deviceContract workDay shift
- ...Quality Specialist - Product Complaints San Diego, CA, United States The Post... ...safety, effectiveness, and regulatory compliance of Hologic's on... ...requirements (FDA, ISO, EU MDR). Conduct initial... ...of in vitro diagnostic or medical device products, ideally with high...RegulatoryComplaintsMedical device
- ...Diego is seeking a Senior Accounts Payable Administrator for the Medical Device Industry. This role involves processing vendor invoices,... ...in Excel, Word, and accounting software. The position offers a hybrid work model after training. #J-18808-Ljbffr QualStaff ResourcesMedical device
- ...Position : Customer Complaints Specialist (Must Trackwise, Complaints Investigations... .../week : 40.00 Client: Medical Device Company Level Of... ...including communication for regulatory compliance with medical device... ...product event status and MDR reportability Assures timeliness...RegulatoryComplaintsMedical deviceContract workWork experience placement
- Seeking a Complaints Engineer to support post-market surveillance activities... ...for globally distributed medical devices. This role will manage... ...handling, vigilance reporting, regulatory compliance, and quality... ...vigilance regulations (FDA, EU MDR, Health Canada, ANVISA, TGA)...RegulatoryComplaintsMedical device
- ...Design Quality Engineer specializing in medical devices in San Diego, CA. This role involves... ...quality across device functionality and regulatory compliance with standards such as IEC 6... ...assessments, and improving quality systems. A hybrid work schedule is available. #J-18808-...RegulatoryMedical device
- ...standards such as FDA (21 CFR 820.198) Complaint handling and (21 CFR 803.3) MDR reporting and company goals.BPO... ...business operation field and or medical device.Minimum of 3-4 years of... ...include complaint handling, and regulatory inspections.Technical and business...RegulatoryComplaintsMedical deviceRemote work
$37.18 per hour
...Complaint Mgmt Spec 2 Medical Devices Company Duration : 12 Months Total Hours/week... ...expertise, data analysis The Specialist, Customer Complaints is... ...communication for regulatory compliance with medical device... ...product event status and MDR reportability Assures...RegulatoryComplaintsMedical deviceContract workWork experience placementLocal areaRemote work$120k - $135k
...Care, Inc. is hiring a Sr. Regulatory Affairs Specialist responsible for developing... ...regulatory strategies for new medical products. The ideal... ...experience in the medical device industry, leading filings and... ...and compliance efforts. This hybrid role offers a mix of in-office...RegulatoryMedical deviceWork at officeRemote work- ...Market Surveillance Specialist will play a crucial... ...market phase. Supports Regulatory Affairs teams through... ...,FDA regulations, EU MDR) and industry standards... ...timely and accurate Medical Device Reporting (MDR) and... ...investigations, including complaint files, investigation...RegulatoryComplaintsMedical deviceMonday to Friday
- ...corrective actions with regulatory requirements, and... ...evaluations of quality signals, complaints, audit findings, and... ...discussions with medical affairs and other relevant... ...experience in medical device Quality Assurance,... ...CFR Part 820, and EU MDR, with the ability to interpret...RegulatoryComplaintsMedical device
- Blue Shield of CA is seeking a Regulatory Complaint Coordinator in San Diego, California. This role involves managing responses to inquiries... ...experience in Appeals and Grievances. The position allows for hybrid virtual work, with expectations to work in office based on...RegulatoryComplaintsWork at office
$67k - $92.6k
...In this role you The Clinical Complaints Specialist will ensure prompt evaluation, investigation, and medical device reporting (MDR) assessment for escalated complaints related... ...Contribute to the success of the Quality & Regulatory / Clinical Wireless Monitoring...RegulatoryComplaintsMedical deviceFull timeWork at officeLocal areaRemote workWork visaRelocation package3 days per week$205.1k - $307.7k
...-driven applications, the regulatory and quality requirements governing... ...those governing physical devices. IEC 62304 compliance,... ...and software-driven medical devices across Illumina's... ...• Manage software-related complaint investigations and MDR/vigilance reporting obligations...RegulatoryComplaintsMedical deviceLocal area- Cypress HCM is seeking a Complaints Engineer in San Diego, California to support post-market surveillance activities for medical devices. The role involves managing complaint handling, vigilance reporting, and regulatory compliance to ensure product safety and customer...RegulatoryComplaintsMedical device
$28.2 - $45.1 per hour
...one of the largest global medical technology companies in the... ...systems while ensuring regulatory compliance, service quality... ...service procedures including complaint handling and Medical Device Reporting. Ensure all... ...tracking. Compliance with MDR and service procedures....RegulatoryComplaintsMedical deviceHourly payWork at officeLocal areaRemote workShift workNight shift- ...Customer Advocacy Technical Specialist Location : San Diego, CA... ...role will be supporting complaint handling for the Infusion Pump... ...working knowledge of medical device regulations Assessment of... ...years’ experience in Quality, Regulatory, or Operations ~ Knowledge...RegulatoryComplaintsMedical deviceContract workDay shift
- A leading medical technology company is seeking a Complaint Compliance Specialist to ensure regulatory compliance in handling complaints. This role entails reviewing complaint records... ...possess 3+ years of experience in medical device complaint handling and a solid...RegulatoryComplaintsMedical deviceFull time
- ...Job Title: Lead System Tester (Medical Devices) Role Overview We are seeking a highly experienced... ...performance, safety, quality, and regulatory requirements throughout the product... ...including design/supplier changes, complaint investigations, CAPA, and lifecycle management...RegulatoryComplaintsMedical device
- ...Position : Complaints Management Specialist - Must SAP, ERP & Order Management (Entry Level) Location : San Diego, CA Duration : 12 Months Total Hours/week : 40.00 1st Shift Client: Medical Device Company Job Category: Healthcare Level Of Experience:...ComplaintsMedical deviceContract workDay shift
- BD is seeking a Complaint Compliance Specialist (Specialist 3) based in California, San Diego. The role involves... ...to ensure complaints conform to regulatory requirements, working closely with quality professionals in the medical device field. Candidates should have a...RegulatoryComplaintsMedical device
- ...Management, Change Control, Deviations, CAPA, Complaints, Training). Facilitate workshops with... ...to internal quality standards, regulatory expectations, and IT/CSV methodologies... ...Life Sciences Quality (Pharma, Biotech, Medical Devices). Hands‑on experience with full Veeva...RegulatoryComplaintsMedical device
- ...the office. The ideal candidate should have a background in medical device or pharmaceutical industries and possess strong organizational... ...skills and attention to detail. The position involves reviewing complaint events, coordinating follow-ups, and managing records using...ComplaintsMedical deviceWork at office
- ...Quality Assurance Specialist 3 San Diego, CA, United States... ...Assurance Specialist 3 within our Regulatory and Quality - Diagnostics... ..., non-conformances, complaints, and Corrective and Preventive... ...Experience with MediaLab and medical device quality system regulations...RegulatoryComplaintsMedical device
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