Global Technical Talent
Product Surveillance Analyst
Global Technical Talent, Minneapolis, Minnesota, United States, 55447
Primary Job Title:
Product Surveillance Analyst
Alternate/Related Job Titles: Complaint Handling Associate Post-Market Surveillance Specialist Quality Compliance Analyst Medical Device Complaint Investigator Regulatory Compliance Analyst
Location: Plymouth, MN Onsite Flexibility: Onsite
Contract Details: Position Type:
Contract Contract Duration:
12 months Start:
10/13/2025 End:
10/12/2026 Pay Rate:
$27.34/hour Shift/Hours:
Monday-Friday, 8:00 AM - 4:30 PM Job Summary: As a
Product Surveillance Analyst , you will support post-market surveillance activities for medical devices within the EP division. This role combines lab work and desk responsibilities to ensure regulatory compliance, accurate complaint handling, and effective product quality monitoring. You will analyze quality records, prepare reports, and contribute to maintaining high standards of safety and reliability.
Key Responsibilities:
Apply
quality principles
to evaluate records, prepare reports, and input data into complaint handling systems. Conduct inspections, verification, and validation of product components and materials. Identify and resolve recurring product or testing issues. Perform lab investigations on returned devices, including handling
biohazardous materials
with PPE. Split duties: approximately 40% lab-based, 60% desk-based. Complete
Hepatitis B screening
as part of onboarding. Write clear reports summarizing findings and results. Utilize systems including
SAP, Winchell, EPIQ, and Microsoft Office . Collaborate with cross-functional teams to support complaint handling and product analysis. Maintain professionalism, critical thinking, and a willingness to learn in an entry-level environment. Required Experience:
Bachelor's degree (preferably in a healthcare or science field). Strong
written and verbal communication skills . Critical thinking and problem-solving abilities. Nice-to-Have Experience:
Post-market surveillance experience within the medical device or pharmaceutical industry. Prior work in complaint handling, investigations, or product analysis. Clinical or lab experience related to medical devices. Knowledge of complaint handling systems such as
EPIQ . Required Skills:
Ability to apply
quality and regulatory principles . Strong attention to detail and analytical mindset. Proficiency in MS Office (Word, Excel, Outlook). Preferred Skills:
Familiarity with
SAP, Winchell, and EPIQ
systems. Experience handling
biohazardous materials
safely. Organizational and reporting skills. Additional Skills:
Willingness to learn and grow within the role. Positive attitude and professional maturity. Ability to work independently and in team environments. Benefits:
Medical, Vision, and Dental Insurance Plans 401k Retirement Fund
About the Client: Global Healthcare Innovator A leading healthcare company dedicated to improving lives worldwide. Their diverse portfolio includes medical devices, diagnostics, nutrition products, and branded generics. The organization is committed to advancing science-driven solutions that empower people to live healthier lives.
About GTT: GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. As a Native American-owned, economically disadvantaged corporation, we highly value diverse and inclusive workplaces. Our clients are Fortune 500 banking, insurance, financial services, and technology companies, along with some of the nation's largest life sciences, biotech, utility, and retail companies across the US and Canada. We look forward to helping you land your next great career opportunity!
Job Number:
25-25977 #gttic #gttjobs
Alternate/Related Job Titles: Complaint Handling Associate Post-Market Surveillance Specialist Quality Compliance Analyst Medical Device Complaint Investigator Regulatory Compliance Analyst
Location: Plymouth, MN Onsite Flexibility: Onsite
Contract Details: Position Type:
Contract Contract Duration:
12 months Start:
10/13/2025 End:
10/12/2026 Pay Rate:
$27.34/hour Shift/Hours:
Monday-Friday, 8:00 AM - 4:30 PM Job Summary: As a
Product Surveillance Analyst , you will support post-market surveillance activities for medical devices within the EP division. This role combines lab work and desk responsibilities to ensure regulatory compliance, accurate complaint handling, and effective product quality monitoring. You will analyze quality records, prepare reports, and contribute to maintaining high standards of safety and reliability.
Key Responsibilities:
Apply
quality principles
to evaluate records, prepare reports, and input data into complaint handling systems. Conduct inspections, verification, and validation of product components and materials. Identify and resolve recurring product or testing issues. Perform lab investigations on returned devices, including handling
biohazardous materials
with PPE. Split duties: approximately 40% lab-based, 60% desk-based. Complete
Hepatitis B screening
as part of onboarding. Write clear reports summarizing findings and results. Utilize systems including
SAP, Winchell, EPIQ, and Microsoft Office . Collaborate with cross-functional teams to support complaint handling and product analysis. Maintain professionalism, critical thinking, and a willingness to learn in an entry-level environment. Required Experience:
Bachelor's degree (preferably in a healthcare or science field). Strong
written and verbal communication skills . Critical thinking and problem-solving abilities. Nice-to-Have Experience:
Post-market surveillance experience within the medical device or pharmaceutical industry. Prior work in complaint handling, investigations, or product analysis. Clinical or lab experience related to medical devices. Knowledge of complaint handling systems such as
EPIQ . Required Skills:
Ability to apply
quality and regulatory principles . Strong attention to detail and analytical mindset. Proficiency in MS Office (Word, Excel, Outlook). Preferred Skills:
Familiarity with
SAP, Winchell, and EPIQ
systems. Experience handling
biohazardous materials
safely. Organizational and reporting skills. Additional Skills:
Willingness to learn and grow within the role. Positive attitude and professional maturity. Ability to work independently and in team environments. Benefits:
Medical, Vision, and Dental Insurance Plans 401k Retirement Fund
About the Client: Global Healthcare Innovator A leading healthcare company dedicated to improving lives worldwide. Their diverse portfolio includes medical devices, diagnostics, nutrition products, and branded generics. The organization is committed to advancing science-driven solutions that empower people to live healthier lives.
About GTT: GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. As a Native American-owned, economically disadvantaged corporation, we highly value diverse and inclusive workplaces. Our clients are Fortune 500 banking, insurance, financial services, and technology companies, along with some of the nation's largest life sciences, biotech, utility, and retail companies across the US and Canada. We look forward to helping you land your next great career opportunity!
Job Number:
25-25977 #gttic #gttjobs