Hybrid Regulatory Complaint Analyst II - Medical Devices
Boston Scientific Corporation
Boston Scientific is seeking a Product Complaint Analyst II to review patient complaints within the Urology portfolio and determine regulatory reportability. The role requires clinical data gathering from multiple sources and precise communication of investigations and outcomes to regulators and internal teams. Hybrid work model with in-office presence required three days per week; relocation assistance is not available. #J-18808-Ljbffr Boston Scientific Corporation
- A leading medical device company in Maple Grove, MN is seeking a Marketing Communications Specialist II to manage Marketing Operations and develop subject matter expertise in industry... .... This is a contract position with hybrid flexibility. #J-18808-Ljbffr Pharmavise CorporationMedical deviceContract work
- Marketing Communications Specialist II — Medical Device (Hybrid — Arbor Lakes, MN) Possible Temp-to-Hire Our F500 Medical Device client has an exciting opportunity for a Marketing Communication Specialist II. Job Summary Manages Marketing Operations business processes,...Medical deviceContract workTemporary work
- ...About the role: The Product Complaint Analyst II will work in a fast-paced... ...CMC) to determine which are regulatory reportable and will coordinate... .... This role follows a hybrid work model requiring employees... ...mandated regulations.Write Medical Device Reports (MDRs), Vigilance,...ComplaintsMedical deviceHourly payWork at officeLocal areaRelocation packageShift work3 days per week
- Work Flexibility: Hybrid or OnsiteThe Senior Manager, Downstream Marketing will lead... ...experiencePreferred:MBA Minimum 4 years of medical device sales or marketing experience Minimum 4... ...is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation...ComplaintsMedical deviceFull timeFor contractorsWork experience placement
- ...measurable impact at Stryker.This is a hybrid role based out of our Bloomington, MN location... ...6 years of experience in marketing or medical device salesPreferred:Graduate degree (MS, MBA... ...is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation...ComplaintsMedical deviceFull timeFor contractors
- ...Job Description R&D Engineer II What You’ll Be Part Of You... ...within a highly regulated medical device manufacturing environment. This... ...and strict compliance with regulatory standards. You’ll... ...related to product issues, complaints, and process improvements...ComplaintsMedical deviceWork at office
$80k - $95k
...For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing... ...comprehensive solutions for Class II and III devices, from design... ...suppliers to resolve CAPA and complaint investigations and in support...ComplaintsMedical deviceWork at office- ...passion for cutting-edge medical technologies, join our... .... This role is Hybrid in Brooklyn Park, MN with... ..., field issues, complaints, and clinical adverse... ...experience in a medical device company Experience... ...FDA QSR and ISO 13485 regulatory requirements, guidelines...ComplaintsMedical deviceWork at officeLocal areaFlexible hours
- Jabil is seeking a Quality Engineer II to ensure product quality and process compliance in medical device manufacturing. You will apply engineering principles and quality tools to drive continuous improvement and robust quality systems. The role supports R&D, manufacturing...Medical device
$68.8k - $123.8k
...globe. How will you make an impact? The Quality Engineer II at Jabil/Nypro Inc. is responsible for ensuring product quality... ...engineering principles and quality tools. This role involves supporting medical device manufacturing operations, driving continuous improvement, and...Medical deviceWork at officeLocal areaWorldwide- ...experience every day.The Principal Regulatory Affairs Specialist will join... ...strategies for innovative medical devices. This individual will be... ...synergy. This role follows a hybrid work model requiring employees... ...strategies for new and modified Class II and Class III medical devices...Medical deviceHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week
$43.37k
...the role: The Urology Complaint Investigation Site (CIS... ...a Quality Technician II to support product complaint... ...for urology devices. This role is responsible... ...synergy. This role follows a hybrid work model requiring... ...experience within the medical device industry Self...ComplaintsMedical deviceHourly payApprenticeshipWork at officeRelocationRelocation packageShift workDay shift3 days per week- ...platforms. The Senior Regulatory Affairs Specialist will... ...synergy. This role follows a hybrid work model requiring... ..., Quality, Clinical, Medical Safety, Operations, Service... ...readiness, including device descriptions,... ...documentation for Class II and Class III medical devices...Medical deviceHourly payWork at officeLocal areaShift work3 days per week
$30 per hour
...Technician Arden Hills, MN | Hybrid (3 Days Onsite) | $30/Hour Join... ...investigation and analysis of advanced medical devices. This temporary Quality Technician II role is ideal for technicians... ...Experience investigating product complaints or device failures Knowledge...ComplaintsMedical deviceTemporary work$75k - $120k
...Engineering with 1-5 years injection molding experience.Medical device industry and validation experience is preferred.Strong... ...documentsAbility to respond to common inquiries or complaints from customers, regulatory agencies or members of the business communityAbility to...ComplaintsMedical deviceFull timeFor contractorsShift work$61.3k - $122.7k
..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,00... ...Opportunity Abbott is seeking a passionate, experienced Regulatory Affairs Specialist II to join our team on-site in Plymouth, MN. This new...Medical deviceFull timeFlexible hours$61.3k - $122.7k
..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,00... ...heart disease. The Opportunity We are recruiting for a Regulatory Affairs Specialist II to join our team on-site in New Brighton, MN. As an...Medical deviceFull timeWork experience placementWorldwide$85k - $110k
...Job Description Job Description A medical manufacturing client in New Hope,... ...and outsourced services integrity, complaint handling, and related CAPA activities... ...) ~ Previous experience with Class II or Class III medical device contract manufacturing complex catheters...ComplaintsMedical deviceContract work- ...As a Quality Systems Engineer II, you will support the... ...synergy. This role follows a hybrid work model requiring employees... ...regulations, ISO 13485, and Medical Device RequirementsApply sound, systematic... ...understanding of nonconformance and CAPA regulatory requirements and best...Medical deviceHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week
$38.69k
..., you'll be supported in progressing - whatever your ambitions. About this role: Receive and disinfect returned complaint-related medical devices. The primary focus is monitoring devices being returned to the laboratory, checking them into the registry system, and...ComplaintsMedical deviceHourly payWork at officeLocal areaRelocationRelocation packageShift work- ...Manufacturing Technician II - Weekend Overnight Shift Work mode: Onsite Onsite Location(s): Maple Grove, MN, US, 55311 Additional... ...Provide technical support or direction to operators and medical device specialists with assistance Support shutdowns (which may include...Medical deviceWork at officeLocal areaRelocation packageNight shiftWeekend work
- ...team in responding to customer complaints using failure analysis... ...Quality Engineer levels I and II Subject matter expert in... ...company Quality System ISO and medical device requirements Read... ...Knowledge of quality systems regulatory requirements and industry standards...ComplaintsMedical deviceFull timeTemporary workWork at office
- ...Maple Grove, MN is seeking a Senior Software Business Analyst to bridge clinical users, business stakeholders, and software teams in the medical device sector. This hybrid, contract role focuses on translating regulatory requirements into actionable software...Medical deviceContract work
- ...Quality Engineer with strong hands-on experience in FDA-regulated medical device manufacturing. Roles & Responsibilities: ~10+ years of... ...13485, FDA 21 CFR Part 820 & Risk Management. ~ Customer complaint investigations & Root Cause Analysis. ~ Manufacturing...ComplaintsMedical deviceContract work
- ...Boston Scientific, customer and regulatory requirements. The position... ..., relocation:This is a hybrid position based at Boston Scientific... ...new information from complaints, CAPAs, nonconformances, clinical... ...5 years' experience in the medical device, pharmaceutical or a...ComplaintsMedical deviceHourly payContract workRelocationRelocation packageShift work
- Integrated Resources, Inc (IRI) is seeking a Recruiter for a hybrid position based in Maple Grove, MN. This role involves high-volume recruiting for Medical Assembler positions, where the candidate will develop sourcing strategies, conduct structured interviews, and prepare...Medical deviceContract workTemporary work
- ...RemoteJob SummaryQuality Engineer II to ensure that products,... ...quality standards and regulatory requirements. The ideal candidate... ...investigations, CAPA, complaint management, and root-cause analysis... ...-solvingExperience in medical-device manufacturing or a regulated...ComplaintsMedical deviceFor contractors
$23.08 - $33.46 per hour
...Overview Cretex Medical is a leading contract manufacturer of... ...and assemblies for the medical device industry. Our customers view... ...uphold product quality and regulatory requirements. The successful... ...and support CAPA and customer complaint processes. Support continuous...ComplaintsMedical deviceHourly payContract workTemporary workLocal area$110k - $150k
...px; padding-top: 15px; } The Regulatory Affairs Specialist applies regulatory... ...business knowledge to ensure medical devices are developed, registered,... ...with FDA Class I and Class II medical devices.Experience... ...assistance or any other protected classification.62415#LI-CO #LI-HYBRIDMedical deviceWork experience placementLocal areaImmediate startFlexible hours$43.37k - $73.74k
...Manufacturing Technician II At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in... ...production floor, working on equipment, and engaging with our Medical Device Specialists (i.e. MDS operators). With general supervision, you...Medical deviceApprenticeshipWork at officeLocal areaRelocation packageMonday to FridayFlexible hoursWeekend workAfternoon shift
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