Manufacturing Associate - 1st Shift

Shift: Monday – Thursday, 5:00am – 3:30pm

Responsibilities

• Set up and run light industrial semi-automated equipment to make a variety of medical devices.

• Operate in-house machines safely – identify emergency stops and stop the process when safety issues are identified, and report safety concerns.

• Conduct quality checks on the produced product to ensure there are no visible defects.

• Document applicable information regarding product quality and machine performance.

• Maintain machines and starts general trouble shooting if needed.

• Visually inspect in-process/finished material while operating – inform designated teammates of any machine malfunction or defective product.

• Start machines, observe for correct operation, and adjust as needed.

• Move empty and full bags/totes/boxes to and from the machine, add labels/weigh product/verify count/add to box/insert into shipper as needed, and stack onto pallet.

• Maintain documentation, production information, cleaning documentation, and safety check documentation in the company system.

• Practice department’s medical manufacturing and housekeeping procedures and complete cleaning verification checklists as required.

• Perform packaging operation off a variety of semi-automated packaging equipment.

• Assemble goods on production line.

Qualifications

We are open to candidates with little to no manufacturing experience. All training is provided starting your first day!

• High School Diploma/GED, preferred

• 0 – 1 year previous work experience, preferred

• Ability to read and follow shop order instructions

What is expected of you and others at this level

• Applies acquired knowledge and skills to complete standard tasks.

• Readily learns and applies new information and methods to work in assigned area.

• Maintains appropriate licenses, training and certifications.

• Works on routine assignments that require some problem resolution.

• Works within clearly defined standard operating procedures and/or scientific methods.

• Adheres to all quality guidelines.

• Works under moderate degree of supervision.

• Work typically involves regular review of output by work lead or supervisor.

• Refers complex unusual problems to supervisor.

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