Top 28 Clinical qa systems and documentation Jobs in Durham Nc

Complaint Reporting MDR/Vigilance Specialist 2
Teleflex —Morrisville, NC
- $73,000 a year
- Background check
- Nursing
- Microsoft Excel
- Paid parental leave
- Health savings account
Compliance - Quality Assurance Analyst
TruTechnologies —Durham, NC
- Full-time
- Bachelor's degree
- Leadership
- Entry level
Senior Specialist Quality Assurance, CSV
Definium Therapeutics —Durham, NC
- $101,147 - $122,757 a year
- Remote
- 7 years
- Psychiatry
- Bachelor's degree
- Health insurance
- Dental insurance
Radiologic Technologist up to $10K Bonus
Concentra —Raleigh, NC
- Full-time
- CPR Certification
- Microsoft Excel
- Vital signs
- Commuter assistance
- Disability insurance
Quality Assurance Specialist
Science Corporation —Durham, NC
- Mid-level
- Continuous improvement
- Fair chance
11d
QA Specialist - Raw Materials
KBI Biopharma —Durham, NC
- Full-time
- Military encouraged
- Senior level
- Commercial
3d
Quality Specialist III
Precision Biosciences —Durham, NC
- 5 years
- Travel
- Senior level
Technical Business Systems Analyst
CEDENT —Durham, NC
- Contract
- 5 years
- SQL
- Senior level
Director, Site Quality - Raleigh
Indivior —Raleigh, NC
- $200,000 - $230,000 a year
- Full-time
- OSHA
- Bachelor of Science
- Master's degree
- Profit sharing
- Employee stock purchase plan
Senior Quality Assurance Associate
WEP Clinical —Morrisville, NC
- Full-time
- Hybrid work
- Microsoft Excel
- Analysis skills
- Bachelor's degree
- Paid parental leave
- Health savings account
5d
Computer System Validation Manager
Ofni Systems —Raleigh, NC
- Computer science
- Computer Science
- Bachelor of Science
Analytics Engineer
Duke Health —Durham, NC
- Full-time
- Hybrid work
- No experience needed
- Mid-level
- SQL
2d
Product Manager, Evidence Generation & Life Sciences Applications
Pedestal Health —Durham, NC
- Writing skills
- Product management
- Organizational skills
- Paid parental leave
- Paid holidays
Clinical Supply Chain Manager, Strategic Development
United Therapeutics —Research Triangle Park, NC
- Full-time
- Hybrid work
- 6 years
- Customer service
- Office
- Paid parental leave
- Employee stock purchase plan
CQV Engineer II/III
HUMACYTE GLOBAL INC —Durham, NC
- Weekends as needed
- Mid-level
- Pediatrics
- Organizational skills
- Paid parental leave
- Paid holidays
Quick Apply
10d
Lead Application Engineer, Field & Clinical Applications
MyEyeDr. —Raleigh, NC
- Full-time
- Hybrid work
- Azure
- Computer Science
- System design
- Paid holidays
- Health insurance
5d
Laboratory MedTech Lead
Millennium Healthcare Management Serv LLC —Durham, NC
- Full-time
- 5 years
- Bachelor's degree
- Organizational skills
- Paid holidays
- Disability insurance
Quick Apply
CRC II (Onsite) - Marietta, GA
サイネオス・ヘルス —Morrisville, NC
- $67,700 - $115,100 a year
- Weekends as needed
- Nursing
- RN License
- Word processing
- Employee stock purchase plan
- Health insurance
Associate Director, Quality Assurance - Regenerative Organ Manufacturing (RMOMAL)
United Therapeutics —Research Triangle Park, NC
- Full-time
- Microsoft Outlook
- Master's degree
- Analysis skills
- Paid parental leave
- Employee stock purchase plan
1d
Sterile Compounding QA Pharmacy Tech III
Duke Health —Durham, NC
- Weekends as needed
- Hospital
- Customer service
- Mid-level
9d

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clinical qa systems and documentation jobs near durham nc

Complaint Reporting MDR/Vigilance Specialist 2

Teleflex -
Morrisville, NC

Apply Now

Job Details

$73,000 a year

Benefits

Paid parental leave
Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Life insurance
Referral program

Qualifications

Customer communication
Microsoft Excel
Microsoft Outlook
Bachelor's degree
Biomedical regulatory compliance
Quality systems

Full Job Description

Date: Jun 15, 2026

Location: Morrisville, NC, US

Company: Teleflex

Expected Travel: Up to 10%

Requisition ID: 13960

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

Position Summary

Work within Complaint Intake & Reporting team to critically review complaints to determine reportability based on the regulatory requirements, risk documentation and clinical experience. Responsible for preparation and timely submissions of MDR/Vigilance reports to FDA/Competent Authorities and other regulatory agencies. Where necessary, seek and document relevant additional information in line with the complaint intake process. Identify potential issues to continuously improve process.

Principal Responsibilities

Utilizes clinical experience in conjunction with risk management documentation to review complaints for adverse event reportability in accordance with US Canadian & European regulations within required time frames.
Follows up with health care providers and customers to provide clarification for complaint files and document correspondence to complaint files as required.
Prepare and submit regulatory reporting documentation such as MedWatch forms with FDA and Vigilance Reports with Canadian and European regulatory authorities.
Assist as clinical liaison for the complaint management department to facilitate understanding of clinical application for product complaint devices and provide training to other team members as required.
Utilize complaint management system to accurately document complaint information.
Final Reviewer/Approval of reporting decisions and initial reports
Support audit activities are required. Assists with responses to FDA and Competent Authority for additional information queries.
Work to meet team KPI’s Department Metrics and over QA/RA goals and objectives.
Support improvement projects in the complaint intake and reporting function.
Support wider QMS and risk management activity as required.

Education / Experience Requirements

B.S. Degree in Nursing, Biomedical Engineering, or related science discipline with a 2-5 years medical device experience, healthcare, quality, accreditation, or regulatory experience.
Experience in Post-Market Surveillance, Complaint Handling, Vigilance Reporting, Quality, Risk Management, Clinical Practice, or healthcare accreditation activities (e.g., Joint Commission) preferred.
Demonstrated knowledge of Medical Device Quality Systems regulations including FDA’s 21 CFR 820, 21 CFR 803, ISO 13485:2016, MDD, EU MDR, MDSAP.

Specialized Skills / Other Requirements

Ability to critically review information and seek clarification.
Ability to work well under deadlines and pressure in a changing environment.
Skilled in use of Microsoft suite of applications i.e., Excel, Outlook, and Word.
The ability to prioritize tasks and be able to manage several tasks simultaneously.
Ability to read understand and self-educate on emerging regulatory requirements.

BEHAVIORS / VALUES

Self-driven and ability to work independently and/or as a team player.
Approachable and enthusiastic. Flexible and adaptable.
Good judgment and problem-solving ability & is capable of understanding the impact of decision making on both Teleflex Medical and their customers.
Experience with risk management - preferred.
Experience with high volume complaints environment - preferred.
Strong organizational, time management, and influence skills with cultural awareness and sensitivity
Excellent verbal and written communication skills with ability to lead meetings.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or [email protected].

Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

Nearest Major Market: Raleigh

Pay: $73,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid parental leave
Paid time off
Parental leave
Referral program
Tuition reimbursement
Vision insurance

Work Location: Hybrid remote in Morrisville, NC 27560

Apply Now

Refine Your Search

clinical qa systems and documentation jobs in durham nc

Complaint Reporting MDR/Vigilance Specialist 2

Compliance - Quality Assurance Analyst

Senior Specialist Quality Assurance, CSV

Radiologic Technologist up to $10K Bonus

Quality Assurance Specialist

QA Specialist - Raw Materials

Quality Specialist III

Technical Business Systems Analyst

Director, Site Quality - Raleigh

Senior Quality Assurance Associate

Computer System Validation Manager

Analytics Engineer

Product Manager, Evidence Generation & Life Sciences Applications

Clinical Supply Chain Manager, Strategic Development

CQV Engineer II/III

Lead Application Engineer, Field & Clinical Applications

Laboratory MedTech Lead

CRC II (Onsite) - Marietta, GA

Associate Director, Quality Assurance - Regenerative Organ Manufacturing (RMOMAL)

Sterile Compounding QA Pharmacy Tech III

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