HemaSource, Inc
Quality Control Analyst – Medical Devices
HemaSource, Inc, Salt Lake City, Utah, United States, 84193
Quality Control Analyst – Medical Devices
Join to apply for the
Quality Control Analyst – Medical Devices
role at
HemaSource, Inc .
HemaSource is looking for a detail-focused and analytical
Quality Control Analyst
to support the intake, evaluation, investigation, and reporting of medical device product complaints. This role directly contributes to patient safety and ensures our products meet global regulatory standards. You will be part of a highly collaborative Quality team that values accuracy, critical thinking, and a commitment to continuous improvement.
If you enjoy problem‑solving, working with technical data, and partnering across Quality, Engineering, and Regulatory teams, this is an excellent opportunity to grow your career in a fast‑paced and mission‑driven environment. You will play a vital role in supporting compliance with FDA regulations, international standards, and internal quality system requirements while helping drive improvements in product performance and customer satisfaction.
Key Responsibilities
Receive, review, and process medical device product complaints, ensuring accurate documentation and timely assessment.
Conduct thorough complaint investigations using root‑cause analysis and cross‑functional input.
Ensure compliance with FDA, ISO 13485, EU MDR, and internal quality system requirements.
Prepare and submit required regulatory reports (MDRs, vigilance reports) within strict timelines.
Analyze complaint data to identify trends and contribute to CAPA and continuous improvement efforts.
Communicate clearly with internal teams and external customers regarding complaint status and findings.
Maintain accurate, audit‑ready records, complaint metrics, and documentation.
Manage LMS activities including training assignments, system maintenance, and compliance reporting.
Qualifications
Bachelor's degree in Life Sciences, Engineering, or related field.
2+ years of medical device complaint handling, post‑market surveillance, or quality experience.
Familiarity with FDA regulations, ISO 13485, EU MDR, and quality system requirements.
Strong analytical, critical‑thinking, and problem‑solving skills.
Excellent written and verbal communication skills.
Proficient with Microsoft Office; experience with QMS/ERP/complaint systems preferred.
Why Join Us
Opportunity to grow in Quality, Regulatory, or Technical Operations.
Meaningful work that directly impacts patient safety and product quality.
Supportive team environment with clear development pathways.
Stable, growing company invested in compliance excellence.
Physical Requirements
Prolonged computer work.
Ability to lift up to 10 lbs. occasionally.
Seniority Level Entry level
Employment Type Full-time
Job Function Quality Assurance
Industries Hospitals and Health Care
Who We Are HemaSource is an innovative logistics solution partner that combines best‑in‑class analytics and high‑quality medical product supply to specialty ambulatory clinics. Our mission is to drive customer operational efficiencies and related cost savings in high volume ambulatory care clinics. HemaSource's patented data analytics software tool and our superior customer service have enabled us to become the preferred disposables provider to the plasma collection market.
Salary: $60000 - $62000 per year
Job Posted by ApplicantPro
Referrals increase your chances of interviewing at HemaSource, Inc by 2x.
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Quality Control Analyst – Medical Devices
role at
HemaSource, Inc .
HemaSource is looking for a detail-focused and analytical
Quality Control Analyst
to support the intake, evaluation, investigation, and reporting of medical device product complaints. This role directly contributes to patient safety and ensures our products meet global regulatory standards. You will be part of a highly collaborative Quality team that values accuracy, critical thinking, and a commitment to continuous improvement.
If you enjoy problem‑solving, working with technical data, and partnering across Quality, Engineering, and Regulatory teams, this is an excellent opportunity to grow your career in a fast‑paced and mission‑driven environment. You will play a vital role in supporting compliance with FDA regulations, international standards, and internal quality system requirements while helping drive improvements in product performance and customer satisfaction.
Key Responsibilities
Receive, review, and process medical device product complaints, ensuring accurate documentation and timely assessment.
Conduct thorough complaint investigations using root‑cause analysis and cross‑functional input.
Ensure compliance with FDA, ISO 13485, EU MDR, and internal quality system requirements.
Prepare and submit required regulatory reports (MDRs, vigilance reports) within strict timelines.
Analyze complaint data to identify trends and contribute to CAPA and continuous improvement efforts.
Communicate clearly with internal teams and external customers regarding complaint status and findings.
Maintain accurate, audit‑ready records, complaint metrics, and documentation.
Manage LMS activities including training assignments, system maintenance, and compliance reporting.
Qualifications
Bachelor's degree in Life Sciences, Engineering, or related field.
2+ years of medical device complaint handling, post‑market surveillance, or quality experience.
Familiarity with FDA regulations, ISO 13485, EU MDR, and quality system requirements.
Strong analytical, critical‑thinking, and problem‑solving skills.
Excellent written and verbal communication skills.
Proficient with Microsoft Office; experience with QMS/ERP/complaint systems preferred.
Why Join Us
Opportunity to grow in Quality, Regulatory, or Technical Operations.
Meaningful work that directly impacts patient safety and product quality.
Supportive team environment with clear development pathways.
Stable, growing company invested in compliance excellence.
Physical Requirements
Prolonged computer work.
Ability to lift up to 10 lbs. occasionally.
Seniority Level Entry level
Employment Type Full-time
Job Function Quality Assurance
Industries Hospitals and Health Care
Who We Are HemaSource is an innovative logistics solution partner that combines best‑in‑class analytics and high‑quality medical product supply to specialty ambulatory clinics. Our mission is to drive customer operational efficiencies and related cost savings in high volume ambulatory care clinics. HemaSource's patented data analytics software tool and our superior customer service have enabled us to become the preferred disposables provider to the plasma collection market.
Salary: $60000 - $62000 per year
Job Posted by ApplicantPro
Referrals increase your chances of interviewing at HemaSource, Inc by 2x.
#J-18808-Ljbffr