JOB TITLE: Quality Engineer

LOCATION: Draper, Utah

SCHEDULE: Standard

DURATION: 6-Month Contract

PAY: $37-42/hr

Interview Process:

Primarily virtual interviews
Final candidate may be invited onsite if local

Job Responsibilities:

In this role, you will support a business-critical production line relocation project within a manufacturing environment. The primary focus will be on validation, qualification, and quality support activities associated with moving production lines between buildings. Key responsibilities include:
Supporting validation and qualification activities tied to manufacturing line transfers.
Creating, executing, and reviewing protocols and reports for requalification and validation efforts.
Assisting with process confirmation activities during manufacturing line moves.
Supporting calibration and verification activities for inspection and testing equipment.
Assisting with physical movement of portable production equipment between facilities as needed.

Essential Duties and Job Functions:
Execute validation protocols and qualification activities related to production line movement projects.
Independently draft and revise validation protocols, reports, and supporting documentation.
Review validation outcomes and ensure documentation aligns with quality requirements.
Support requalification of manufacturing processes following equipment relocation.
Coordinate with project engineers and manufacturing teams to maintain project timelines.
Participate in process confirmation activities to ensure transferred lines meet operational standards.
Assist with calibration and functional verification of inspection and testing equipment.
Work cross-functionally with manufacturing, engineering, and quality stakeholders to resolve issues efficiently.
Contribute to aggressive project timelines while maintaining documentation accuracy and compliance.

Knowledge & Skills:
Strong written and verbal communication skills.
Analytical problem-solving ability with strong attention to detail.
Ability to work independently with limited oversight.
Comfortable operating in fast-moving and evolving project environments.
Strong documentation discipline and protocol-writing capability.
Ability to collaborate effectively across multiple stakeholders in manufacturing settings.
Team-oriented with the ability to integrate quickly into established teams.
Decisive and proactive in driving assigned tasks forward.

Education & Experience:
Bachelor's degree in Engineering (required).
2-4 years of experience as a Quality Engineer.
Experience in medical device or regulated manufacturing environment strongly preferred.
Hands-on experience with validation and qualification activities.
Background in manufacturing line validation, inspection methods, and test methods.
Experience supporting equipment moves, production line transfers, or requalification activities preferred.

What Makes Someone Successful Here:
Quickly builds relationships and navigates cross-functional teams effectively.
Can independently own tasks such as writing validation protocols from start to finish.
Remains productive in ambiguous or evolving project conditions.
Comfortable making decisions without requiring heavy oversight.

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Hydrogen Group

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