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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