Product Complaints Investigator III - Medical Device
Greenville, North Carolina, United States · On-site
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Full-time
bachelor degree
Medical insurance, Dental insurance, Vision insurance, Paid time off, Holidays, 401k company match
Posted 3d ago
~40 hrs/week
Responsibilities
The QA Specialist III leads end-to-end product complaint investigations and provides technical oversight to ensure compliance with cGMP regulations. They partner with cross-functional teams to drive root cause analysis, risk assessments, and effective corrective actions.
Requirements
Candidates must hold a bachelor's degree in a health science, life science, or engineering discipline. A minimum of 4 years of progressive experience in the pharmaceutical or biotechnology industry is required.
Full job description
Work Schedule
First Shift (Days)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus. The operation specializes in taking both sterile injectable and oral solid dose drug products from development phase through commercialization.
Medical, Dental, & Vision benefits-effective Day 1
Paid Time Off & Holidays
401K Company Match up to 5%
Tuition Reimbursement – eligible after 90 days!
Employee Referral Bonus
Employee Discount Program
Recognition Program
Charitable Gift Matching
Company Paid Parental Leave
Career Advancement Opportunities
Location/Division Specific Information
Greenville, NC
RELOCATION ASSISTANCE IS NOT PROVIDED
Must be legally authorized to work in the United States WITHOUT SPONSORSHIP OF ANY KIND NOW OR IN THE FUTURE.
Must be able to pass a comprehensive background check, which includes a drug screen.
Discover Impactful Work:
The QA Specialist III, Product Complaints provides technical leadership and independent Quality oversight for the investigation and resolution of product complaints in a regulated pharmaceutical CDMO environment. This role ensures compliance with global regulatory requirements while protecting patient safety, product quality, and customer confidence.
You will serve as a key technical and regulatory resource for complaint investigations, partnering cross-functionally to drive effective root cause analysis, risk assessment, and corrective actions that prevent recurrence and support continuous improvement.
A Day in the Life:
Lead end-to-end product complaint investigations of moderate to high complexity.
Conduct root cause analysis, risk assessments, and document investigations in compliance with cGMPs and quality systems.
Evaluate product quality, patient safety, and regulatory impact while escalating critical issues appropriately.
Serve as a technical and regulatory resource for complaint investigations.
Partner with Manufacturing, QC, Regulatory, Supply Chain, and customers to resolve complaints.
Drive timely and effective CAPA implementation.
Author and revise complaint procedures, work instructions, and investigation reports.
Support regulatory inspections, audits, and customer audits.
Manage multiple priorities in a fast-paced manufacturing environment.
Mentor junior complaint investigators.
Serve as QA Supervisor designee when required.
Perform other duties as assigned.
Keys to Success:
Education
Associate’s or Bachelor’s degree in health science, life science, engineering, or related discipline and a minimum of 6 years of work experience
Experience
Minimum of 4 years of total experience within combination products or medical device industry
Experience conducting GMP investigations involving combination product or medical device complaints, deviations, or quality events strongly preferred.
CDMO and/or sterile manufacturing experience is a plus.
Knowledge, Skills, Abilities
Strong knowledge of cGMP regulations, quality systems, and pharmaceutical manufacturing.
Ability to independently assess complex quality issues and risk.
Excellent written and verbal communication skills.
Strong organizational skills with ability to manage multiple priorities.
Excellent documentation and attention to detail.
Self-motivated with ability to work independently.
Comfortable working in a fast-paced regulated manufacturing environment.
Physical Requirements / Work Environment
Requires standing, walking, sitting, lifting up to 35 pounds, manual dexterity, visual acuity, and prolonged computer use in an office/manufacturing environment.
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
For more information, please visit www.thermofisher.com.
Offices: 168 Third Avenue, Waltham, MA, US
Analytical InstrumentsLaboratory Supply Chain Programs and eCommerceLaboratory EquipmentLab ServicesSpecialty DiagnosticsLife SciencesPharma Servicesand CDMOElectronicsHealth Care
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
For more information, please visit www.thermofisher.com.
Offices: 168 Third Avenue, Waltham, MA, US
Analytical InstrumentsLaboratory Supply Chain Programs and eCommerceLaboratory EquipmentLab ServicesSpecialty DiagnosticsLife SciencesPharma Servicesand CDMOElectronicsHealth Care