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Job Requirements of Manufacturing Engineer III:
-
Employment Type:
Contractor
-
Location:
Maple Grove, MN (Onsite)
Do you meet the requirements for this job?
Manufacturing Engineer III
Careers Integrated Resources Inc
Maple Grove, MN (Onsite)
Contractor
Job Title: Manufacturing Engineer III
Location: Maple Grove, MN, 55311
Duration: 12 Months+ Tempt to hire
Pay Range: $40 to $55/hr. on W2
Shift: Work shift: 1 st Shift (Hybrid) (In office - Tuesday, Wednesday Thursday)
Role Overview:
Key Requirements:
Skills:
Preferred qualifications:
Location: Maple Grove, MN, 55311
Duration: 12 Months+ Tempt to hire
Pay Range: $40 to $55/hr. on W2
Shift: Work shift: 1 st Shift (Hybrid) (In office - Tuesday, Wednesday Thursday)
Role Overview:
- The Supplier Engineer (SE) role focuses on leading remediation activities for supplier processes and quality compliance in medical device manufacturing.
- It involves reviewing and improving supplier documentation (like PFMEA), validating processes and inspections, and managing changes to meet updated standards.
- The role requires close collaboration with suppliers and internal teams to ensure all quality requirements are met, with a strong emphasis on patient safety, product quality, and regulatory compliance.
Key Requirements:
- 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 Client's 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 Client functional resources to complete all activities needed to approve supplier’s process risk documentation and process/inspection validations to the newly defined criteria.
- In all actions, it 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.
Skills:
- Bachelor’s degree in engineering
- 1 – 2 years of experience in a manufacturing environment.
- Experience with installation qualifications (IQ), operational qualifications (OQ), performance qualification (PQ), and test method validation (TMV).
- Ability to travel up to 15% of the time (mostly domestic, could be international).
Preferred qualifications:
- Experience working with suppliers or in supply chain management.
- Experience working in the Medical Device Field.
- Excellent communication and project management skills.
- Strong bias for action and results oriented.
- Self-driven and self-motivated to learn and apply knowledge to produce results.
- Good understanding of statistical methods, six sigma methodologies, and problem-solving methodologies.
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