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Sr. Reliability Engineer

Development Resource Group, Inc.

Mounds View, MNContract$40–55/hrSeen 1w agoSeen in employer's feed 2 days ago

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At a glance

Compensation
$40–55/hr
Location
Mounds View, MN
Schedule
Contract
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Reliability Engineer supports Quality Systems activities for medical device products across multiple manufacturing sites. The role partners with manufacturing, quality, engineering, and regulatory teams on CAPA, Change Control, Validation, and post-market quality initiatives. Responsibilities include supporting investigations and reviews, participating in audits, and collaborating to resolve quality issues and drive continuous improvement.

Skills & qualifications

RequiredNice to have

Skills

Quality SystemsCAPAChange ControlValidationMedical Device RegulationsQuality AuditsRegulatory AuditsProject ManagementProgram ManagementCross-Functional CollaborationManufacturing Support

Qualifications

Bachelor's Degree in Relevant Field5+ Years Medical Device Experience

Benefits

Medical Insurance
401(k) Match
Paid Time Off

Full job description

Job Duties

We are seeking an experienced Reliability Engineer to support Quality Systems activities for medical device products. This role will partner with manufacturing, quality, engineering, and regulatory teams to drive CAPA, Change Control, Validation, and post-market quality initiatives across multiple sites.

Key Responsibilities

  • Support Quality Systems activities across multiple manufacturing sites.

  • Lead and support CAPA investigations, implementation, and effectiveness reviews.

  • Support Change Control, Validation, and post-market quality deliverables.

  • Participate in Quality and Regulatory Audit activities.

  • Collaborate cross-functionally to resolve quality issues and drive continuous improvement.

Minimum Education Required

Bachelor's Degree in a relevant field

Minimum Experience Required

Required Qualifications

  • 5-15 years of experience in the medical device industry.

  • Strong experience with Quality Systems, CAPA, Change Control, and Validations.

  • Knowledge of medical device regulatory requirements.

  • Experience supporting Quality and Regulatory Audits.

  • Strong project/program management and cross-functional collaboration skills.

Top Skills

  • Manufacturing Support

  • Project & Program Support

  • CAPA Management & Cross-Functional Collaboration

Shift

First (Day)

Number of Openings

1

Public Transportation Accessible

Yes

Veterans Encouraged to Apply

Yes

Physical Required

No

Drug Test Required

Yes

Compensation

$40.00 - $55.00 / Hourly

Postal Code

55112

Job Type

Contract (W2)

Place of Work

On-site

Requisition ID

6797

Job Benefits

Health Insurance, Life Insurance, 401k retirement plan, paid sick time

Application Instructions

If interested and qualified, please submit your resume to [email protected] or visit our website to apply: http://dr-group.com/find-engineering-technical-jobs/

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