QA Specialist DHR
Job Location:
Irving, TX - USA
Hourly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
Location: Irving TX
Onsite Flexibility: Onsite
- Position Type: Contract
- Contract Duration: 6 months
- Pay Rate: $28.75 / Hour (USD)
- Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
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This role supports the final release of finished medical device products by reviewing Device History Records (DHR) for accuracy completeness and compliance. The QA Specialist will verify that released products meet established quality standards before shipment and work across cross-functional teams to resolve issues and support continuous improvement.
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- Support final release of finished medical device products.
- Review Device History Records (DHR) for accuracy completeness and compliance.
- Verify that released products meet established quality standards before shipment.
- Review both 3rd floor Instrument products and ACP jobs.
- Identify documentation errors and escalate quality issues as needed.
- Collaborate with cross-functional teams to resolve issues and support continuous improvement.
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- Strong attention to detail
- Effective communication
- Problem-solving ability
- Teamwork and collaboration
- Ability to work independently with minimal supervision
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- Quality Assurance (QA) experience
- Batch Release experience
- Non-conformance documentation
- Process improvement involvement
- Quality Assurance background is a plus
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- High School Diploma or equivalent required
- Bachelors degree preferred
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- 02 years of quality manufacturing or documentation review experience.
- Ability to work with minimal guidance and follow defined procedures.
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- Previous Device History Record (DHR) experience (hiring managers top preference)
- Experience in a highly regulated manufacturing environment
- Closely related manufacturing experience
- Quality-related background including quality documentation quality analysis or quality engineering
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- Must be physically fit and comfortable performing the positions physical requirements.
- Must be comfortable with the level of the role and scope.
- Local candidates are preferred for the on-site interview.
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- Interview process: Initial phone interview followed by an on-site interview.
- The hiring manager may consider candidates overqualified if they have supervisory or management experience a masters degree (unless a recent graduate) extensive experience concentrated in one specialized area or a significantly more advanced background than the position requires.
- Candidates who demonstrate a pattern of frequent job changes multiple short-term positions without a clear explanation or limited stability or progression in their employment history are not a fit for this role.
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- Medical Vision and Dental Insurance Plans
- 401k Retirement Fund
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This global healthcare innovator has been advancing medical technology for more than 140 years operating in over 160 countries with a diverse portfolio spanning medical devices diagnostics nutritional products and established pharmaceuticals. The organization employs biomedical engineers clinical scientists regulatory affairs specialists and commercial operations professionals across four major business segments including cardiovascular care diabetes management diagnostic testing and nutrition and is a certified Great Place to Work with 80 percent of employees reporting it as a great place to work well above the national average.
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GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking financial services technology life sciences biotech utilities and retail sectors throughout the U.S. and Canada.
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Job Number: 26-12368
Industry: Manufacturing & Operations
Required Experience:
IC
