Cleanroom Final Assembly Technician I

Artivion; Austin (TX); On-site; USD 40,000 - 54,000; Full time

Job summary

Artivion in Austin, TX is seeking a Final Assembly Technician I to perform workstation assembly of heart valve components in a sterile cleanroom. You will sew cuffs to specification, inspect parts with a microscope, and maintain accurate production records to keep manufacturing on schedule.

The role requires basic computer skills and the ability to read manufacturing instructions and drawings. You will work in compliance with FDA/ISO practices, support cleanroom operations, and contribute to

Qualifications

• High school diploma or equivalent.
• Experience in manufacturing environment preferred.
• Experience in inspection or assembly or similar intricate hand work preferred.
• Experience with FDA & ISO manufacturing practices preferred.
• Basic computer skills including MS Office, internet, and email.
• Ability to read and understand detailed manufacturing instructions and drawings.
• Ability to use a microscope.

Responsibilities

• Sew and assemble cuffs to specification in a cleanroom.
• Inspect materials and assemblies with a microscope.
• Maintain production and inspection records.
• Assist with monitoring, cleaning, and testing cleanroom environment.
• Batch components for the day’s production.
• Know how to sew all Mitrals, Aortics and Conform_X product lines.
• Quality first mentality in all job functions.
• Maintain high quality alongside production targets.
• Adhere to Clean Room GMP in behavior and attire.

Skills

Manual dexterity

Attention to detail

Reading drawings

Microscope operation

Basic computer skills

FDA & ISO awareness

Education

High school diploma or equivalent

Tools

MS Office

Internet

Email

Job description

Artivion in Austin, TX is seeking a Final Assembly Technician I to perform workstation assembly of heart valve components in a sterile cleanroom. You will sew cuffs to specification, inspect parts with a microscope, and maintain accurate production records to keep manufacturing on schedule.

The role requires basic computer skills and the ability to read manufacturing instructions and drawings. You will work in compliance with FDA/ISO practices, support cleanroom operations, and contribute to