Artivion, Inc.
Quality Control Inspector I (Tuesday-Saturday, 7:00 am - 3:30 pm)
Artivion, Inc., Austin, Texas, us, 78716
Quality Control Inspector I (Monday-Thursday, 2:00 pm - 12:30 am)
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Quality Control Inspector I (Monday-Thursday, 2:00 pm - 12:30 am)
role at
Artivion, Inc.
Company Overview 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.
Position Objective The Quality Control Inspector will review device history records and document their work on the DHR. Inspect components utilizing inspection equipment. Visually and dimensionally inspect for conformance to specification while following written guidelines.
Responsibilities
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.
Qualifications
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 for the first few months
Other responsibilities as assigned.
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.
Seniority level
Entry level
Employment type
Full‑time
Job function
Quality Assurance
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Quality Control Inspector I (Monday-Thursday, 2:00 pm - 12:30 am)
role at
Artivion, Inc.
Company Overview 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.
Position Objective The Quality Control Inspector will review device history records and document their work on the DHR. Inspect components utilizing inspection equipment. Visually and dimensionally inspect for conformance to specification while following written guidelines.
Responsibilities
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.
Qualifications
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 for the first few months
Other responsibilities as assigned.
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.
Seniority level
Entry level
Employment type
Full‑time
Job function
Quality Assurance
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