As an Associate MDR/Vigilance Specialist, you will document, evaluate, and process product feedback and complaint information to determine complaint recordability and regulatory reporting ...
As an Associate MDR/Vigilance Specialist, you will document, evaluate, and process product feedback and complaint information to determine complaint recordability and regulatory reporting ...
As an Associate MDR/Vigilance Specialist, you will document, evaluate, and process product feedback and complaint information to determine complaint recordability and regulatory reporting ...
As an Associate MDR/Vigilance Specialist, you will document, evaluate, and process product feedback and complaint information to determine complaint recordability and regulatory reporting ...
A Day in the Life The Associate MDR/Vigilance Specialist supports the Post Market Quality organization by evaluating product feedback and complaint information for medical devices and determining ...
A Day in the Life The Associate MDR/Vigilance Specialist supports the Post Market Quality organization by evaluating product feedback and complaint information for medical devices and determining ...
A Day in the Life The Associate MDR/Vigilance Specialist supports the Post Market Quality organization by evaluating product feedback and complaint information for medical devices and determining ...
A Day in the Life The Associate MDR/Vigilance Specialist supports the Post Market Quality organization by evaluating product feedback and complaint information for medical devices and determining ...
Assoc MDR/Vigilance Spec
Moundsview, MN · On-site
Associate MDR/Vigilance Specialist Client: Medical Device Manufacturing Company Location: Mounds View, MN 55112 Duration: 2 Years + Possible Extension Shift: 1st Shift | Onsite Description: Job ...
Assoc MDR/Vigilance Spec
Moundsview, MN · On-site
Associate MDR/Vigilance Specialist Client: Medical Device Manufacturing Company Location: Mounds View, MN 55112 Duration: 2 Years + Possible Extension Shift: 1st Shift | Onsite Description: Job ...
Medical Device Vigilance professionals
Raleigh, NC · On-site
$40 - $42/hr
Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - fully Onsite - 3 days a week in office requirement (flexible days) for 6 months, WFH 2 days a week.
Medical Device Vigilance professionals
Raleigh, NC · On-site
$40 - $42/hr
Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - fully Onsite - 3 days a week in office requirement (flexible days) for 6 months, WFH 2 days a week.
Associate MDR/Vigilance Specialists are responsible for theintake, documentation, Medical Device Reporting, and investigation of complaintsfor legacy Neuromodulation products in accordance with ...
Associate MDR/Vigilance Specialists are responsible for theintake, documentation, Medical Device Reporting, and investigation of complaintsfor legacy Neuromodulation products in accordance with ...
Patient Service Representative (Remote - Full Time)
Thousand Oaks, CA · Remote
$16 - $18/hr
Vigilance Health is seeking a Patient Service Representative (PSR) who will serve as the front-line ... Associate degree preferred. * 1+ year in healthcare customer service or call center. * Bilingual in ...
Quick apply
Patient Service Representative (Remote - Full Time)
Thousand Oaks, CA · Remote
$16 - $18/hr
Vigilance Health is seeking a Patient Service Representative (PSR) who will serve as the front-line ... Associate degree preferred. * 1+ year in healthcare customer service or call center. * Bilingual in ...
Patient Service Representative (Remote - Full Time)
$18 - $22.75/hr
Vigilance Health is seeking a Patient Service Representative (PSR) who will serve as the front-line ... Associate degree preferred. * 1+ year in healthcare customer service or call center. * Bilingual in ...
Patient Service Representative (Remote - Full Time)
$18 - $22.75/hr
Vigilance Health is seeking a Patient Service Representative (PSR) who will serve as the front-line ... Associate degree preferred. * 1+ year in healthcare customer service or call center. * Bilingual in ...
Client Growth & Marketing Coordinator
Las Vegas, NV · Remote
$43K - $59K/yr
Vigilance Health is a patient engagement organization that partners with community health centers ... Associate's or Bachelor's degree in Business, Marketing, Healthcare, or related field preferred ...
Quick apply
Client Growth & Marketing Coordinator
Las Vegas, NV · Remote
$43K - $59K/yr
Vigilance Health is a patient engagement organization that partners with community health centers ... Associate's or Bachelor's degree in Business, Marketing, Healthcare, or related field preferred ...
Patient Service Representative (Remote - Full Time)
Thousand Oaks, CA · On-site +1
$16 - $18/hr
Vigilance Health is seeking a Patient Service Representative (PSR) who will serve as the front-line ... Associate degree preferred. * 1+ year in healthcare customer service or call center. * Bilingual in ...
Patient Service Representative (Remote - Full Time)
Thousand Oaks, CA · On-site +1
$16 - $18/hr
Vigilance Health is seeking a Patient Service Representative (PSR) who will serve as the front-line ... Associate degree preferred. * 1+ year in healthcare customer service or call center. * Bilingual in ...
Client Growth & Marketing Coordinator
Las Vegas, NV · On-site
$40K - $55K/yr
Vigilance Health is a patient engagement organization that partners with community health centers ... Associate's or Bachelor's degree in Business, Marketing, Healthcare, or related field preferred ...
Client Growth & Marketing Coordinator
Las Vegas, NV · On-site
$40K - $55K/yr
Vigilance Health is a patient engagement organization that partners with community health centers ... Associate's or Bachelor's degree in Business, Marketing, Healthcare, or related field preferred ...
Food Production Associate
San Antonio, TX · On-site
$16/hr
The Food Production Associate is responsible for performing various tasks including culling ... Keen Vigilance upholding quality and standards is a must. * Packaging finished goods, ensuring that ...
Food Production Associate
San Antonio, TX · On-site
$16/hr
The Food Production Associate is responsible for performing various tasks including culling ... Keen Vigilance upholding quality and standards is a must. * Packaging finished goods, ensuring that ...
Security Associate
Arlington, TX · On-site
$21/hr
Ultimately, the Security Associate helps protect the integrity of the manufacturing operations and promotes a culture of safety and vigilance throughout the organization. Minimum Qualifications:
Quick apply
Security Associate
Arlington, TX · On-site
$21/hr
Ultimately, the Security Associate helps protect the integrity of the manufacturing operations and promotes a culture of safety and vigilance throughout the organization. Minimum Qualifications:
Lead Intensive Supports Associate
Anchorage, AK · On-site
$22.43 - $26.36/hr
Providing continual heightened vigilance in supervision and monitoring required for the safety of ... Associate's degree in Human Services, Health or Social Science, Special Education or other related ...
Lead Intensive Supports Associate
Anchorage, AK · On-site
$22.43 - $26.36/hr
Providing continual heightened vigilance in supervision and monitoring required for the safety of ... Associate's degree in Human Services, Health or Social Science, Special Education or other related ...
Loss Prevention Associate
Fort Mill, SC · On-site
$16.75/hr
Maintain vigilance through patrols, security audits, and the use of advanced tools and technology ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...
Quick apply
Loss Prevention Associate
Fort Mill, SC · On-site
$16.75/hr
Maintain vigilance through patrols, security audits, and the use of advanced tools and technology ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...
Lead Intensive Supports Associate
Anchorage, AK · On-site
$18 - $21.75/hr
... Support Associate) to join our team in Anchorage, Alaska . Hope Community Resources, Inc. is a ... Providing continual heightened vigilance in supervision and monitoring required for the safety of ...
Lead Intensive Supports Associate
Anchorage, AK · On-site
$18 - $21.75/hr
... Support Associate) to join our team in Anchorage, Alaska . Hope Community Resources, Inc. is a ... Providing continual heightened vigilance in supervision and monitoring required for the safety of ...
Associate Manager, Product Surveillance
Racine, WI · On-site
$80 - $100/hr
A Brief Overview The Associate Manager, Product Surveillance is responsible for providing tactical ... Submit MDRs and Vigilance Reports according to regulatory timelines. * Maintain awareness of ...
Associate Manager, Product Surveillance
Racine, WI · On-site
$80 - $100/hr
A Brief Overview The Associate Manager, Product Surveillance is responsible for providing tactical ... Submit MDRs and Vigilance Reports according to regulatory timelines. * Maintain awareness of ...
A Brief Overview The Associate Manager, Product Surveillance is responsible for providing tactical ... Submit MDRs and Vigilance Reports according to regulatory timelines. * Maintain awareness of ...
A Brief Overview The Associate Manager, Product Surveillance is responsible for providing tactical ... Submit MDRs and Vigilance Reports according to regulatory timelines. * Maintain awareness of ...
A Brief Overview The Associate Manager, Product Surveillance is responsible for providing tactical ... Submit MDRs and Vigilance Reports according to regulatory timelines. * Maintain awareness of ...
A Brief Overview The Associate Manager, Product Surveillance is responsible for providing tactical ... Submit MDRs and Vigilance Reports according to regulatory timelines. * Maintain awareness of ...
Associate Vigilance information
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Associate MDR/Vigilance Specialist
Moundsview, MN • On-site
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 9 days ago
Key responsibilities
Review product feedback, complaint information, and product analysis results to determine complaint status and regulatory reporting requirements.
Assess adverse events and product performance issues in accordance with United States and international regulatory reporting criteria.
Prepare and compile Medical Device Reports (MDRs) and other regulatory submissions required by regulatory agencies.
Medtronic rating
7.9
Based on 180 frontline employees who took The Breakroom Quiz
155th of 547 rated manufacturers
Job description
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the LifeThe Neuromodulation and Pelvic Health business is focused on therapies that help improve quality of life for patients living with chronic conditions. Within this organization, the MDR/Vigilance team supports global post-market surveillance and complaint handling activities to help ensure product quality, patient safety, and regulatory compliance. The team partners across Quality, Regulatory Affairs, Engineering, and Clinical organizations to evaluate product feedback and support regulatory reporting requirements.This position is located in Mounds View, Minnesota and follows an onsite work model with a minimum of four days per week onsite. No travel is required.
Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver results...the right way. That's the Medtronic Mindset - our cultural norms. Our brand is rooted in action, not just words. The Medtronic Mindset defines the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your extraordinary potential to ensure future generations live better, healthier lives.
As an Associate MDR/Vigilance Specialist, you will document, evaluate, and process product feedback and complaint information to determine complaint recordability and regulatory reporting requirements for medical devices. This role supports regulatory compliance activities, complaint closure processes, and cross-functional collaboration to ensure timely and accurate assessment of product performance and patient safety events.
Primary Responsibilities
Review product feedback, complaint information, and product analysis results to determine complaint status and regulatory reporting requirements.
Assess adverse events and product performance issues in accordance with United States and international regulatory reporting criteria.
Prepare and compile Medical Device Reports (MDRs) and other regulatory submissions required by regulatory agencies.
Monitor complaint records and associated activities to support timely complaint review and closure.
Ensure complete, accurate, and compliant documentation within complaint handling and post-market surveillance systems.
Analyze complaint, investigation, and clinical data to support safety assessments and data quality initiatives.
Partner with cross-functional teams to obtain information needed for complaint investigations and regulatory reporting activities.
Support the development and continuous improvement of complaint handling and vigilance processes.
Required Qualifications
Bachelor's degree and 0 years of relevant experience.
Ability to review and document product complaints and adverse event information with a high level of accuracy and attention to detail.
Ability to interpret and follow established procedures, regulatory requirements, and quality system documentation.
Strong written and verbal communication skills for collaboration with cross-functional stakeholders.
Preferred Qualifications
At least 6 months of experience processing complaints through the complaint handling process from intake through investigation.
Experience within a medical device, pharmaceutical, biotechnology, or other regulated industry.
Experience with Medical Device Reporting (MDR), vigilance, post-market surveillance, or complaint handling activities.
Product and therapy experience related to Neuromodulation and Pelvic Health.
Experience using Global Complaint Handling (GCH) systems.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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