New · posted Nov 6
Artivion · Medical Devices
Quality Control Inspector I
- Austin, TX
- On-site
- Full-time
- Associate & Specialist
The role
- Location: Austin, TX
- Schedule: Tuesday - Saturday 7:00am - 3:30pm
Position Objective
The Quality Control Inspector will review device history records & document their work on the DHR. Inspect components utilizing inspection equipment. Visually and dimensionally inspect for conformance to specification while following written guidelines.
What you need
- 1 year of experience in a manufacturing environment, preferred
- High School diploma or equivalent
- Reading and understanding written data and instruction
- Good or corrected eyesight for visual inspection and microscope use
- Good manual dexterity for handling small parts
- Ability to tolerate use of acetone and reagent alcohol
- Organized work habits and attention to detail is a must
- Good communication and interpersonal skills
- Required to read, write and speak English with good command of the language, follow verbal and written instructions and use simple math
- Basic computer skills including at minimum, be adept in use of MS Office, internet, and electronic mail
- Ability to read, analyze, and interpret written instructions
- Previous experience with quality systems is desirable
- Must be available to train Monday - Friday 7 am - 3:30 pm for the first few months
What you'll do
- Perform visual and dimensional inspection on components and subassemblies utilizing various precision equipment.
- Perform quarantine and receiving inspection of incoming raw materials, controlled manufacturing materials, machined components, labeling instrumentation, and packaging materials. Inspect for conformance to specifications.
- Verify all equipment used is currently calibrated if required.
- Review processing and inspection data for completeness of operations, accuracy of data, traceability of product and materials, and disposition of non-conforming product.
- Using your judgement, interface with other department personnel to clarify, collaborate, and/or correct the information provided, and to solicit required information.
- Maintain documentation of all functions.
- Utilize electronic systems to maintain training records.
- Monitor and maintain processing materials and equipment.
- Verify all equipment used is currently calibrated if required.
Other responsibilities as assigned.
Pay and benefits
Artivion didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
5weeks
Generous Time Off: Enjoy 5 weeks of Paid Time Off (PTO), accrued throughout the year, plus 10 paid company holidays
Health & Wellness: Comprehensive medical, dental, and vision coverage, along with life insurance and supplemental benefits
4%
Retirement Planning: 401(k) with up to a 4% company match (Traditional and Roth options available)
Employee Stock Purchase Plan: Purchase Artivion stock at a discounted rate and share in our company’s success
Work-Life Balance: Benefit from a consistent and predictable work schedule
Education Support: Tuition reimbursement to support your continued growth and development
Employee Assistance Program (EAP): Access confidential resources for personal, financial, and emotional well-being
Legal Benefits (LegalShield): Includes legal consultation, document review, will preparation, and 24/7 emergency access
Financial Wellness: Access tools and resources through the Truist Momentum program
Employee Discounts: Enjoy savings through Working Advantage, offering discounts on travel, entertainment, and more
Efficient Hiring Process: We value your time and offer a streamlined interview process with timely feedback and decisions
We offer a comprehensive and competitive benefits package designed to support your health, financial well-being, and work-life balance:
Where you'll work
Austin, TXOn-siteOpen in Maps (opens in a new tab)
More jobs in Austin, TX
From the posting
About Artivion
Headquartered in suburban Atlanta, Georgia, Artivion, Inc. specializes in developing innovative medical devices aimed at addressing challenging cardiac and vascular conditions. Our Austin facility houses a diverse team dedicated to producing the On-X Mechanical Heart Valves. With over 1,600 employees globally and manufacturing sites in Atlanta, Austin, and Hechingen, Germany, Artivion serves healthcare professionals in over 100 countries. For more details on the On-X Mechanical Heart Valve, click here.
Equal opportunity, accessibility and legal noticesArtivion's statements, word for word
Equal Employment Opportunity Employer (EEO):
We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected status under applicable law.
Job intelligence
The context around this role
Live data · November 6, 2026
Salary intelligence
How the pay compares
Associate & Specialist roles in the US53 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $46,000 | $48,000 | $51,500 |
Comparisons: the base pay employers published on open Quality Inspection roles at the same level on Regulatory Jobs, November 6, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Inspection
The general path across 98 open Quality Inspection roles on Regulatory Jobs, with the titles they carry most. Not Artivion's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 26 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance5
- Collaboration and leadership4
- Documentation and SOPs3
- Data and digital systems2
- Lab testing and methods1
- Investigations and CAPA1
- Regulatory submissions1
- Quality systems and risk1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Inspection work in medical devices, each linked to the agency or standards body that publishes it.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- FDA21 CFR Part 801(official source, opens in a new tab)FDA labeling requirements for medical devices
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- FDA21 CFR Part 830 (UDI)(official source, opens in a new tab)Unique device identification and the GUDID database
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ISOISO 15223-1(official source, opens in a new tab)Symbols for medical device labels and labeling
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
Company hiring pulse
Artivion on Regulatory Jobs
- 11
- Open roles
- 11
- Distinct roles
- 2
- Locations
By discipline
- Quality4 36%
- Clinical4 36%
- Regulatory3 27%
By level
- Senior & Principal4 36%
- Associate & Specialist4 36%
- Manager2 18%
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Quality Control Inspector I at Artivion
Open until filled.