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Operator I_MN - 2nd Shift

Job in Minneapolis, Hennepin County, Minnesota, 55442, USA
Listing for: HireTalent
Full Time position
Listed on 2026-07-17
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Production QC/QA, Manufacturing & Industrial Operations
Job Description & How to Apply Below
Position: Operator I_MN ONLY - 2nd Shift
POSITION TITLE:

Manufacturing Assembly Operator (Medical Devices)
JOB TYPE:
Entry-Level / Full-Time

LOCATION:

Plymouth, MN, 55442
TIME: 4:00 PM 2:30 AM
If Selected Interview will be held on: 7/21/2026 from 4 pm - 6 pm
Mandatory Training: 4 days - 8 am to 4:30pm
________________________________________

EVENT & CHECK-IN INSTRUCTIONS
" Arrival:
Please have candidates arrive at the Main Entrance on the West side of the building.
" Check-In:
Upon arrival, they will need to check in with the front desk.
" Point of Contact:
Candidates should ask the receptionist for Lameck Gisemba, Wantree Yang, and Ryan Payne.
________________________________________

TOP 5 REQUIRED SKILLS
1. Entry-level assembly aptitude (medical device experience is a plus).
2. Good hand-eye coordination and manual dexterity.
3. Ability to follow written and verbal instructions.
4. Basic quality awareness and inspection skills.
5. Reliability and ability to work in a team-oriented production environment.
________________________________________

PHYSICAL & ENVIRONMENTAL REQUIREMENTS
" Microscope Use:
Yes some microscope use is required for inspection and assembly tasks.
" Team Lifts

Required:

No no routine team lifting is required; however, the role may require fast-paced movements.
" Standing vs. Sitting Ratio:
Varies by station (approximately 40-50% sitting / 40-50% standing).
________________________________________

POSITION SUMMARY
This position is responsible for the production of high-quality medical devices within a manufacturing cell. Working under close supervision, the employee may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies. Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.
________________________________________

KEY RESPONSIBILITIES
" Ensure that relevant job documentation for cell operations and functions is accurate and up to date.
" Clearly communicate ideas, problems, and solutions to all levels of manufacturing management in both written and oral form.
" Maintain a positive attitude when interacting with internal customers and external customers (such as tours).
" Follow safety guidelines and utilize appropriate safety devices when performing all operations.
" Participate in continuous improvement/quality initiatives in order to enhance production processes and achieve quality and profitability metrics.
" Maintain accurate records to ensure traveler and quality documents are correct, all parts are traceable, and quality issues can be addressed to assure the quality of all products.
" Demonstrate a basic understanding of Lean Manufacturing.
" Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
" Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
" Read, comprehend, and follow written procedures; understand and follow verbal instructions.
" Utilize electronic data collection systems and computer software packages.
" Prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
" Handle and maneuver small components and parts.
" Make critical decisions and judgments with minimal supervision.
________________________________________

QUALIFICATIONS
"

Education:

High school diploma or equivalent is preferred.
"

Skills:

Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions.
"

Experience:

Entry-level assembly aptitude; medical device experience is a plus.
________________________________________

DRESS CODE POLICY (FOR INTERVIEW TOUR & ON-THE-JOB)
All candidates must adhere to the following dress code during the interview tour and while working in the production area:

Clothing General Requirements:
" Clothing must be non-shedding and free of frayed hems or loose threads.
" Tassels, fringes, glitter, sequins (sewn or glued on), and any other items that could become dislodged are not allowed on clothing.
" Fabric Test:
Pull at the fabric tightly with your fingers. If fibers are dislodged, the garment may not be worn in the production area.
" Prohibited Fabrics:
Sweaters, sweater vests, loose-fiber garments, loose knits, or fleece may not be worn.
" All clothing must be clean and free of visible contamination (sand, mud, dirt, lint, etc.).

Upper Body:
" All clothing from the waist up must fit under the lab coat/gown.
" Turtle necks or high-necked clothing shall not stick out above the neck of the lab coat/gown.
" Sleeves shall not stick out beyond the cuff of the lab coat/gown.

Headwear:
" Caps, hats, scarves, or bandanas shall not be worn under the bouffant.
" Head wraps/scarves worn to accommodate customs:
Must be covered with the…
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