Quality Engineer I

Primary Talent Partners; Plymouth (MN); On-site; USD 48,000 - 62,000; Full time

Benefits offered by this job

ACA-compliant supplemental package

Job summary

Primary Talent Partners has a new contract opening for a Quality Engineer I with our medical device client in Plymouth, MN. This is a 12-month contract with a potential for extension.

The role involves overseeing quality standards, collaborating with engineering and manufacturing teams, and implementing testing and inspection processes to ensure compliance and reliability across production lines.

Qualifications

• 2-5 years of quality engineering experience.

Responsibilities

• Project management execution
• Process validation new label software migration and printer roll out for entire manufacturing site
• Line support for manufacturing

Skills

Process Validation

Manufacturing Support

Self starter

Job description

Primary Talent Partners has a new contract opening for a Quality Engineer I with our medical device client in Plymouth, MN. This is a 12-month contract with a potential for extension.

Pay

$35.00 - $45.00/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship.

Description

Responsibilities may include the following and other duties may be assigned:

• Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

Top 3 skill sets required

• Process Validation
• Manufacturing Support
• Self starter

3 main responsibilities/day to day activities required for this role

• Project management execution
• Process validation new label software migration and printer roll out for entire manufacturing site
• Line support for manufacturing

What products (if any) will this role support

• Product are peripheral vascular business - primary stents, balloon catheters, embolization capture device and extrusion

What is your target years of experience

2-5 yrs

Equal Opportunity

Primary Talent Partners is an Equal Opportunity /Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at [e-mail]

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