Production Associate II - 1st Shift - $21.85/hr

Stryker; Salt Lake City (UT); On-site; USD 40,000 - 60,000; Full time

Job summary

A leading medical device company is seeking a Production Associate II for their onsite facility in Salt Lake City. The role involves assembly, inspection, and ensuring quality for critical components. Ideal candidates have at least a High School diploma and experience in manufacturing, preferably within a clean room environment. This position offers opportunities for professional growth while upholding high standards of quality and efficiency.

Qualifications

• 1+ years of experience in manufacturing or medical devices.
• Experience in clean room environment preferred.

Responsibilities

• Prepare, assemble, and inspect electrical and mechanical components.
• Maintain clean room standards and quality adherence.
• Operate manufacturing equipment and support continuous improvements.

Skills

Manual Work

Lean Manufacturing Principles

Quality Assurance

Education

High School or GED

Job description

Work Flexibility: Onsite

1st Shift: Mon - Thurs 4:00AM - 2:30PM

What you will do:

As a Production Associate II, you will prepare, process, clean, install, assemble, rework, verify, test, and/or inspect electrical and mechanical components, hardware, subassemblies, and assemblies on single or multiple product lines

• Advanced manual work such as UV Bond, soldering, crimping, stent loading, etc.
• Maintain clean room standards per standard operating procedure.
• Maintain responsibility for quality and adherence to manufacturing process requirements
• Build product by following all processes in which certified and completing other assigned work, while meeting manufacturing goals and metrics
• Record information, perform verifications, and maintain accurate records on shop floor paperwork
• Demonstrate and apply a solid understanding of Lean Manufacturing principles
• Handle, transport, store, and inspect components and final assembly devices
• Sets up and operates manufacturing equipment
• Train/certify others on process steps as directed by Supervisor
• Red line documents in need of correction and assist with resolution
• Execute validation protocols and engineering evaluations with supervision
• Support continuous improvements through idea submission and leading assigned projects
• Meet work schedule and overtime requirements, including weekends

What you need:

Preferred Qualifications

• High School or GED
• 1+ years of Manufacturing or Medical Device Experience
• Clean room Experience

Physical & Cognitive Requirements:

• Requires ability to lift/carry 10-50 lbs. on a frequent basis depending on site and product line, may rarely lift/carry 50-75 lbs
• Job demands include prolonged stooping, kneeling, crouching, bending, sitting, standing and/or crawling as appropriate
• May be required to reach, push or pull in order to accomplish job accountabilities
• Requires hand grasp ability

Travel Percentage: None Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.