QA Specialist I

Abbott; Irving (TX); On-site; USD 30,000 - 39,000; Full time

Benefits offered by this job

Medical plan

Dental plan

Vision plan

Health Savings Account

Flexible Spending Accounts

401(k)

Job summary

Abbott in Irving, TX is seeking a QA Specialist I for a 6-month, on-site assignment. You will support final release of finished medical devices, review DHRs for accuracy and compliance, and verify released products meet quality standards prior to shipment.

Ideal candidates have a high school diploma with 2+ years of quality documentation experience, or recent life-sciences graduates. You will collaborate with cross-functional teams, identify documentation errors, and participate in continuous

Qualifications

• High school diploma with 2+ years of quality documentation experience.
• Open to recent Bachelor graduates in life-sciences or Biology field.
• 0–2 years of quality, manufacturing, or documentation review experience.
• Ability to work with minimal guidance and follow defined procedures.

Responsibilities

• 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 prior to shipment.
• Review both 3rd floor Instrument products and ACP jobs.
• Identify documentation errors and elevate quality issues as needed.
• Collaborate with cross functional teams to resolve issues and support continuous improvement.

Skills

Attention to detail

Quality Assurance

Communication

Problem solving

Teamwork

Independent work

Education

High School diploma

Bachelor's degree in life sciences

Job description

QA Specialist I

Location: Irving, TX

Duration: 6 Month (with Possibility of extension)

100% On-Site

Shift: 7AM - 4PM

Job Duties

• 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 prior to shipment.
• Review both 3rd floor Instrument products and ACP jobs.
• Identify documentation errors and elevate quality issues as needed.
• Collaborate with cross functional teams to resolve issues and support continuous improvement.

Required Experience

• High School diploma with 2+ years of relevant Quality documentation experience
• Open to Recent Bachelor graduates in life-sciences OR Biology Feild.
• 0–2 years of quality, manufacturing, or documentation review experience.
• Ability to work with minimal guidance and follow defined procedures.

Key Skills

• Strong attention to detail
• Quality Assurant background is a plus
• Effective communication
• Problem solving ability
• Teamwork and collaboration
• Ability to work independently with minimal supervision

Preferred Experience

• Quality Assurance (QA) experience
• Batch Release experience
• Non-Conformance documentation
• Process improvement involvement

Consultants Eligible Benefits Upon Waiting Period

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High-Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs