QA Specialist DHR
Irving, TX - USA
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.
This role supports the final release of finished medical device products with a primary focus on reviewing Device History Records (DHR) for accuracy completeness and compliance.
- 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.
- Strong attention to detail
- Effective communication
- Problem-solving ability
- Teamwork and collaboration
- Ability to work independently with minimal supervision
- Quality Assurance background is a plus
- Quality Assurance (QA) experience
- Batch Release experience
- Non-conformance documentation
- Process improvement involvement
- High School Diploma or equivalent required
- Bachelors degree preferred
- 02 years of quality manufacturing or documentation review experience.
- Ability to work with minimal guidance and follow defined procedures.
- Medical Vision and Dental Insurance Plans
- 401k Retirement Fund
This global healthcare innovator has been advancing medical technology for more than 140 years delivering life-changing solutions across medical devices diagnostics nutritional science and pharmaceutical products to patients in more than 160 countries. The organizations portfolio spans cardiovascular care diabetes management diagnostic testing nutrition and neuromodulation with recognized brands that millions of people rely on every day. Operating across four major business segments medical devices nutritional products diagnostics and established pharmaceuticals this organization employs biomedical engineers clinical scientists regulatory affairs specialists and commercial operations professionals who collaborate across cross-functional international teams. Certified as a Great Place to Work with 80 percent of employees reporting it as a great place to work well above the national average this company offers real resources for development meaningful mission alignment and a culture grounded in inclusion and innovation.
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.
Job Number: 26-12368
Industry: Manufacturing & Operations
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Required Experience:
IC