Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

REQ SOLUTIONS

Supplier Manufacturing Engineer

Career Insights for Manufacturing Engineer (General)

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Minnesota data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Manufacturing Engineer uses technology and engineering to help companies and organizations manufacture products with efficient use of time, resources, and energy.

$89,013 / year median in Minnesota

-1% projected decline

Explore Career

Job Description

Supplier Manufacturing Engineer at

REQ SOLUTIONS

Supplier Manufacturing Engineer at

REQ SOLUTIONS

in Maple Grove, Minnesota Posted in 1 day ago.

Type:

full-time

Job Title:
Supplier Manufacturing Engineer Duration:

12+ Months (Possible temp to hire)

Location:

Maple Grove, MN 55311

Hybrid Role Responsibilities:

Supplier Engineer (SE) will be responsible for the remediation activities identified by

CAPA 7720

for contract manufactured (CM) sourced finished medical device (SFMD) product. This individual works independently, serves as a leader for SE remediation activities, and interacts cross-functionally with team members and CM SFMD suppliers to execute deliverables according to business needs. Review, remediate, and approve CM SFMD supplier's process risk documentation (PFMEA) to newly defined criteria. Review, remediate, and approve CM SFMD supplier's process and inspection validations to statistical requirements. Perform change management activities to remediate gaps found in CM SFMD Supplier's process risk documentation and process/inspection validations. Collaborate with CM SFMD suppliers and functional resources to complete all activities needed to approve supplier's process risk documentation and process/inspection validations to the newly defined criteria. Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Education/Experience:

Bachelor's degree in engineering is required! 2-5 years of experience in a manufacturing environment. Problem solving, being able to showcase examples Manufacturing experience Validation experience Change management experience Ability to travel up to 15% of the time. (Domestic possible.) Preferred qualifications: Experience working with suppliers or in supply chain management. Experience working in the Medical Device Field. Experience with installation qualifications (IQ), operational qualifications (OQ), performance qualification (PQ), and test method validation (TMV). Excellent communication and project management skills.