Redbock - an NES Fircroft company
Quality Lab Technician
Redbock - an NES Fircroft company, Minneapolis, Minnesota, United States, 55400
Redbock - an NES Fircroft company provided pay range
This range is provided by Redbock - an NES Fircroft company. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $20.00/hr - $28.50/hr
Quality Lab Technician III (24 month contract // Minneapolis, MN) Top Needs:
Confident with computer‑based systems and detailed documentation
Open to biohazard product cleaning and decontamination, including products returned with blood and tissue (with training provided and appropriate safety measures in place)
Motivation and satisfaction in structured, routine work
Education Required:
High school diploma or equivalent
Years’ Experience Required:
2+ years of relevant experience
Summary:
We are seeking a reliable, detail‑oriented Technician II to join our Returned Product Analysis Intake Lab team. In this role, you’ll be responsible for receiving, cleaning, and documenting receipt of returned, explanted medical devices. Your work will directly support our commitment to patient safety, regulatory compliance, and continuous product improvement. This is an ideal opportunity for someone who thrives on structure, takes pride in precision, and enjoys being part of a collaborative, dependable team.
Duties:
Receive, inspect, and document returned implantable medical devices such as pacemakers, defibrillators, and leads
Perform cleaning and decontamination of products in a biosafety level II (BSL‑2) laboratory environment, following strict safety and quality procedures
Record device details and case information accurately in electronic systems
Identify and communicate potential product complaints to internal quality and complaint‑handling teams
Package and prepare devices for shipment to manufacturing and analysis partners
Maintain lab equipment, cleanliness, and organization to uphold safety and compliance standards
Partner with Analysis teams to ensure consistent, high‑quality documentation
Requirements:
High school diploma or equivalent required & 2+ years of relevant work experience
Strong attention to detail and accuracy in documentation
Comfortable working in a BSL‑2 lab environment with appropriate personal protective equipment (PPE)
Proficiency with Microsoft Office and other standard computer applications
Self‑motivated and dependable, with strong communication and teamwork skills
Previous experience in a laboratory, medical device, or regulated environment preferred
Willingness to comply with Hepatitis A/B and Tetanus vaccination requirements
Willingness to work in PPE gowning for the majority of the workday
Comfortable with repetitive, process‑based tasks and able to maintain a steady workflow
Demonstrated ability to elevate concerns or uncertainties effectively and in a timely manner
Efficiency‑minded – someone who enjoys checking things off, streamlining routines, and staying productive
Familiarity with Microsoft Outlook or other email/calendar tools for communication
Proficiency with basic spreadsheet tools (e.g., Microsoft Excel or Google Sheets) for data entry and tracking
Strong written and verbal communication skills – clear, concise, and structured communication is essential
Nice to Have:
1‑3 years of Medical Device industry experience
Familiarity with decontamination, sterilization, or lab protocols
Familiarity with FDA medical device quality system regulations i.e. FDA 21 CFR Part 820, EU 217/745 (EU MDR), ISO 13485, ISO 14971, IEC 60601.
Knowledge of Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS.
Strong written and verbal communication skills and ability to work cooperatively as part of a cross‑functional team.
Benefits
401(k)
Vision insurance
Disability insurance
Medical insurance
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Base pay range $20.00/hr - $28.50/hr
Quality Lab Technician III (24 month contract // Minneapolis, MN) Top Needs:
Confident with computer‑based systems and detailed documentation
Open to biohazard product cleaning and decontamination, including products returned with blood and tissue (with training provided and appropriate safety measures in place)
Motivation and satisfaction in structured, routine work
Education Required:
High school diploma or equivalent
Years’ Experience Required:
2+ years of relevant experience
Summary:
We are seeking a reliable, detail‑oriented Technician II to join our Returned Product Analysis Intake Lab team. In this role, you’ll be responsible for receiving, cleaning, and documenting receipt of returned, explanted medical devices. Your work will directly support our commitment to patient safety, regulatory compliance, and continuous product improvement. This is an ideal opportunity for someone who thrives on structure, takes pride in precision, and enjoys being part of a collaborative, dependable team.
Duties:
Receive, inspect, and document returned implantable medical devices such as pacemakers, defibrillators, and leads
Perform cleaning and decontamination of products in a biosafety level II (BSL‑2) laboratory environment, following strict safety and quality procedures
Record device details and case information accurately in electronic systems
Identify and communicate potential product complaints to internal quality and complaint‑handling teams
Package and prepare devices for shipment to manufacturing and analysis partners
Maintain lab equipment, cleanliness, and organization to uphold safety and compliance standards
Partner with Analysis teams to ensure consistent, high‑quality documentation
Requirements:
High school diploma or equivalent required & 2+ years of relevant work experience
Strong attention to detail and accuracy in documentation
Comfortable working in a BSL‑2 lab environment with appropriate personal protective equipment (PPE)
Proficiency with Microsoft Office and other standard computer applications
Self‑motivated and dependable, with strong communication and teamwork skills
Previous experience in a laboratory, medical device, or regulated environment preferred
Willingness to comply with Hepatitis A/B and Tetanus vaccination requirements
Willingness to work in PPE gowning for the majority of the workday
Comfortable with repetitive, process‑based tasks and able to maintain a steady workflow
Demonstrated ability to elevate concerns or uncertainties effectively and in a timely manner
Efficiency‑minded – someone who enjoys checking things off, streamlining routines, and staying productive
Familiarity with Microsoft Outlook or other email/calendar tools for communication
Proficiency with basic spreadsheet tools (e.g., Microsoft Excel or Google Sheets) for data entry and tracking
Strong written and verbal communication skills – clear, concise, and structured communication is essential
Nice to Have:
1‑3 years of Medical Device industry experience
Familiarity with decontamination, sterilization, or lab protocols
Familiarity with FDA medical device quality system regulations i.e. FDA 21 CFR Part 820, EU 217/745 (EU MDR), ISO 13485, ISO 14971, IEC 60601.
Knowledge of Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS.
Strong written and verbal communication skills and ability to work cooperatively as part of a cross‑functional team.
Benefits
401(k)
Vision insurance
Disability insurance
Medical insurance
#J-18808-Ljbffr