Hybrid Regulatory Complaint Analyst II - Medical Devices
Boston Scientific
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
- 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
- ...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
- 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
- ...passion for cutting‑edge medical technologies, join our... ...the end‑to‑end complaint management process. This... ...and in alignment with regulatory and internal requirements... ...office conditions - hybrid work environment available... ...background in medical devices, healthcare or a...ComplaintsMedical deviceWork at officeLocal areaFlexible hours
- Boston Scientific in Minnesota is seeking a Regulatory Affairs Specialist I to support product... ..., and global registrations across the medical device lifecycle. Working with cross-... ...and high quality standards. This is a hybrid role with in-office presence required at...Medical deviceWork at office3 days per week
$49.61k
...a Field Service Technician II at Boston Scientific, you will... ...Boston Scientific medical systems and devices. This is a hands-on, field-... ...include support for sales, complaint resolution, event coverage,... ...guidelines, and applicable regulatory requirements Participate...ComplaintsMedical deviceHourly payWork experience placementWork at officeRemote workShift work- ...ENGINEER II - Medical Device Product Development & Manufacturing Engineering (Vascular Access Devices... ...Management System and applicable regulatory requirements. The role escalates novel... ...support for nonconformances, CAPAs, and complaint investigations. Complaint...ComplaintsMedical deviceFull timeWork at office
- Experis is seeking a Buyer II in Plymouth, MN to join the procurement team. The role focuses on direct materials purchasing, ERP... ...offering opportunities to enhance cross-functional procurement skills in a medical device/manufacturing environment. #J-18808-Ljbffr ExperisMedical deviceRemote jobShift work
- ...Quality Engineer II At Jabil/Nypro Inc.At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering... ...principles and quality tools. This role involves supporting medical device manufacturing operations, driving continuous improvement, and...Medical deviceWork at officeLocal areaWorldwide
$68.8k - $123.8k
...Quality Engineer II At Jabil/Nypro Inc.At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering... ...principles and quality tools. This role involves supporting medical device manufacturing operations, driving continuous improvement, and...Medical deviceWork at officeLocal areaWorldwide$75k - $112.6k
...Engineer IIThe Quality Engineer II will be responsible for... ...team in responding to customer complaints using failure analysis,... ...company Quality System, ISO, and medical device requirementsRead, understand... ...of quality systems, regulatory requirements, and industry standardsIntermediate...ComplaintsMedical deviceHourly payTemporary workWork at officeLocal area$71.5k
...day. Join the Urology Complaint Investigation Site (CIS) department... .... This role follows a hybrid work model requiring... ...that meet organizational and regulatory requirements. ● Champion continuous... ..., preferably within the medical device industry. ● Experience supporting...ComplaintsMedical deviceHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week- Abbott is seeking a Regulatory Affairs Specialist II to work on-site in Plymouth, MN. This role requires strong attention to detail and effective... ...global regulatory activities for implantable medical devices. With 2-3 years of experience in a regulated industry,...Medical device
- ...to execute and support the Complaint Handling, Regulatory Reporting, and Post Market... ...responsible for reviewing device history records for nonconformities... ...Surveillance Engineer II.Audit Support:You will be... ...years’ relevant experience (medical device or other regulated industry...ComplaintsMedical deviceWork at officeImmediate start
- Job Title: Regulatory Affairs Specialist II Location: Minneapolis, MN 55401, US (Primary) Education: Bachelor's Degree Career Level: Experienced... ...experience. 3-5 years' experience in regulated medical device industry highly preferred. Knowledge of global Class I...Medical deviceFull timeWork at office
$61.3k - $122.7k
...Regulatory Affairs Specialist II Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,00...Medical deviceFlexible hours- ...compliance activities related to complaint handling and ensuring adherence to regulatory requirements. Qualified... ...degree and at least 7 years in the medical device industry. A strong background in... ...preferred. The position requires hybrid work, with at least three days in...ComplaintsMedical deviceWork at office
$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$60k - $120k
.... Employees can qualify for free medical coverage in our Health Investment Plan... ...seeking a passionate, experienced Regulatory Affairs Specialist II to join our team on-site in Plymouth... ...Electrophysiology Mapping and Imaging devices to achieve departmental and...Medical deviceFor contractorsWorldwideShift work$61.3k - $122.7k
...of. Employees can qualify for free medical coverage in our Health Investment Plan... ...seeking a passionate, experienced Regulatory Affairs Specialist II to join our team on-site in Plymouth... ...submission/approval implantable medical devices is preferred. What You’ll Work On...Medical deviceWork at officeShift work- ...manufactures components or finished devices for BSC distribution. The... ...to assess compliance with regulatory standards and Boston Scientific... ...quality issues.Investigates complaints and manages SCARs/NCEPs at... ...relevant experience.Experience in medical device, automotive,...ComplaintsMedical deviceHourly payShift work
$43.37k
...About the role: As a Manufacturing Engineer Technician II, you support the factory floor by ensuring equipment and processes... ...savings Provide technical support or direction to operators and medical device specialists with assistance Support shutdowns (which may...Medical deviceHourly payWork at officeLocal areaRelocationRelocation packageShift workAfternoon shift$107.2k - $160.8k
...padding-left: 17px; padding-top: 15px; } he Regulatory Affairs Specialist is responsible for... ..., including audit responses.Review complaints identified as potentially reportable... ...’ experience in regulatory affairs in Medical Device industryFamiliarity with FDA and EU regulations...ComplaintsMedical deviceWork at officeLocal areaImmediate startFlexible hours- ...Quality Engineer with strong hands-on experience in FDA-regulated medical device manufacturing.Roles & Responsibilities:10+ years of Quality... ...of ISO 13485, FDA 21 CFR Part 820 & Risk Management.Customer complaint investigations & Root Cause Analysis.Manufacturing readiness,...ComplaintsMedical deviceContract work
- ...supplier engineering, operations, regulatory, post market) focuses on... ...and synergy. This hybrid role is based at the Arbor Lakes... ...recently launched and established medical devices against risk... ...workExperience with design changes, complaint risks, and corrective action...ComplaintsMedical deviceHourly payRelocation packageShift work3 days per week
$16 - $17 per hour
...provider is seeking a QA Technician to ensure the integrity of reprocessed medical devices. The role involves following protocols for quality control, conducting audits, and investigating complaints. Ideal candidates will have over 5 years of experience in a production...ComplaintsMedical deviceHourly pay- ...culture where engineers do meaningful work.The Quality Engineer II will provide engineering support at Boston Scientific's Weaver... ...qualifications:Bachelor's degree in engineering.Experience in the medical device industry.Experience with manufacturing or process engineering,...Medical device
$106.8k
...associated with Boston Scientific’s complaint handling program in accordance with corporate... ...with U.S. and international medical device regulatory requirements related to complaint handling... ...incentives as applicable. Work Model Hybrid: employees are required to work in...ComplaintsMedical deviceWork at officeLocal areaRelocation package3 days per week- ...Plymouth, MN seeks a Design Assurance Engineer II to lead development projects and ensure design verification/validation for medical devices. The role requires coordinating cross‑functional teams and aligning outputs to regulatory expectations and production controls....Medical device
- ...Sr Medical Safety Specialist - Endoscopy Work mode: Hybrid Onsite Location(s): Maple Grove, MN, US, 5... ...closely with Clinical, Regulatory, Quality, Post Market Surveillance, the Complaint Management Center and cross... ...portfolio of medical devices across one or more...ComplaintsMedical deviceWork at officeLocal areaRelocationRelocation package3 days per week
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