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MATERIAL HANDLER COORDINATOR - 2026-6246
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SUPPLY CHAIN / PROCUREMENT MANAGER - 2026-6275
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PRODUCTION OPERATOR ASSEMBLER II- 1ST SHIFT - 2026-6278
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PRODUCTION OPERATOR ASSEMBLER II - 2ND SHIFT - 2026-6282
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PRODUCTION OPERATOR ASSEMBLER I - PLATINUM 2ND OPS - 2026-6228
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PRODUCTION TECHNICIAN - 1ST SHIFT METALS - 2026-6248
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LASER TURRET OPERATOR - 2ND SHIFT - 2026-6250
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STAGING PRODUCTION TECHNICIAN - 2026-6219
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PRODUCTION SUPERVISOR - 2ND SHIFT - 2026-6230
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MANUAL GRINDER - 2026-6202
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PRODUCTION OPERATOR ASSEMBLER I - ADDITIVE ASSEMBLY - 2026-6194
Coon Rapids, MN
PRODUCTION OPERATOR ASSEMBLER I - ADDITIVE DEBURRING - 2026-6195
Coon Rapids, MN
PRODUCTION OPERATOR ASSEMBLER II - 2ND SHIFT - 2026-6282
Bloomington, MNAbout QTS
QTS offers critical end-of-line services for medical device OEMs including finished device assembly, packaging and sterilization management. QTS was founded in 2001 and is part of the Cretex Medical family of companies.
- Purpose: To have a positive impact on people.
- Mission: Make it easier to get products to patients.
- Values: Integrity, Collaboration, Communication, & Leadership
Learn more at www.qtspackaging.com and www.cretexmedical.com.
Responsibilities
Position Summary
The Production Operator Assembler II is an intermediate-level role responsible for performing complex machine operations, assembly, inspection, and secondary processes. This position requires proficiency in multiple production areas, troubleshooting skills, and the ability to work independently while maintaining quality and safety standards.
This position will be based out of our facility located in west Bloomington, Minnesota (55438). The hours for 2nd shift are 2:45pm-1:15am.
Essential Job Functions
Core Responsibilities (Applies to All Areas)
- Perform visual and/or dimensional inspection using microscopes, gauges, calipers, or other measurement tools, as required.
- Complete required documentation such as production records, quality checks, setup sheets, and history records.
- Participate in continuous improvement initiatives and implement process enhancements.
- Handle and work with cleaning chemicals such as isopropyl alcohol, detergents, or solvents when needed.
- Maintain an organized, clean work area following 5S expectations.
- Participate in required training and company meetings.
- Read, understand, and follow work instructions, standard work, and applicable quality/ISO/cGMP requirements.
- Crosstrain across manufacturing areas.
- Support and comply with the Quality System, ISO, and medical device regulatory requirements.
- Communicate issues with materials, equipment, or processes promptly.
- Perform other duties as assigned.
The following responsibilities may vary by operating company and may not apply in all cases. Other responsibilities may also be assigned, but are not listed below.
Assembly Responsibilities
- Inspect, assemble, and/or package components and medical devices per customer specifications.
- Operate hand tools and basic manual equipment used in the assembly process.
- Use sealing equipment such as tray, band, or impulse sealers.
- Perform labeling, packaging, and final presentation of product.
Production Operations Responsibilities
- Operate production equipment or machines per work instructions, ensuring correct materials, tooling, programs, and processes are used.
- Monitor production processes, part quality, and machine performance and escalate as needed.
- Perform basic preventive or operator-level machine checks (e.g., cleanliness, safe operation).
Secondary Operations Responsibilities
- Perform secondary operations such as trimming, deburring, cleaning, laser marking, laser welding and/or finishing of components.
- Operate designated secondary equipment or simple mechanical devices.
- Inspect and verify part conformance after secondary operations.
- Use basic measurement tools to ensure accuracy (gauge pins, calipers, drop indicators, pull testers, tape measures, etc.).
Qualifications
Minimum Requirements, Education & Experience (incl. KSA’s and certifications)
- Ability to work in a manufacturing environment.
- Ability to read, write, and follow written instructions in English.
- Perform basic math, hand–eye coordination, and dexterity.
- Ability to use basic hand tools and measurement equipment.
- Clear and effective verbal and written communication skills.
- Strong attention to detail and organizational skills.
- Ability to work in a fast-paced team environment and handle multiple tasks.
- Proficiency with Microsoft Office (Outlook, Word, Excel, PowerPoint)
Desirable Criteria & Qualifications
- High school diploma or equivalent.
- 6+ months of manufacturing, assembly, machine operation, or cleanroom experience.
- Familiarity with FDA, ISO, cGMP, Lean manufacturing, or workplace safety practices.
- Experience working with microscopes or inspection tools.
What Is It Like to Work for QTS?
At QTS, we are passionate about quality as the services we provide have a direct impact on the quality of life for others and we pride ourselves on our culture and work environment. The tenure of our staff ranges from recently hired to 20+ years! Check out some of things that employees have said about working at QTS:
- "We are a family."
"After so many toxic work environments, coming to QTS was like finding a harbor in a storm! Coming here was one of the best professional decisions I’ve ever made!”
- "I would describe my coworkers as kind and friendly."
- "Three words that I would use to describe QTS's culture are: Respectful, Fast-paced, and Fun!"
We encourage you to explore the many opportunities that Quality Tech Services could offer you as an employee and as a valued team member.




