Cleanroom Sewing Assembly Tech

Scorpion Therapeutics; Austin (TX); On-site; USD 40,000 - 52,000; Full time

Job summary

Scorpion Therapeutics is seeking a Final Assembly Technician I to join our medical device manufacturing team in a cleanroom environment. You will sew cuffs, assemble heart valve components, inspect parts with a microscope, and record production data to ensure quality and compliance.

Expect standard shifts with overtime and weekend coverage as needed. Candidates should be able to stand for long periods, lift moderate weights, and follow GMP and safety protocols in a highly regulated setting.

Qualifications

• High school diploma or equivalent.
• Experience in manufacturing, inspection, or assembly preferred.
• Basic computer skills required; ability to read instructions.
• Ability to interpret manufacturing instructions and operate microscopes.

Responsibilities

• Sew cuffs for Mitrals, Aortics, and Conform_X product lines.
• Inspect components with microscopes.
• Record production data.
• Support cleanroom cleanliness and safety protocols.

Skills

Basic computer skills

Interpret manufacturing instructions

Manual dexterity

Attention to detail

Education

High school diploma or equivalent

Tools

Microscope operation

Job description

Role:

Final Assembly Technician I in a medical device manufacturing environment, focusing on sewing, assembling, and inspecting heart valve components in a cleanroom setting. Objectives include ensuring high-quality production, adherence to specifications, and maintaining a safe, compliant workspace.

Responsibilities:

• sewing sewing cuffs for Mitrals, Aortics, and Conform_X product lines
• inspecting components with microscopes
• recording production data
• supporting cleanroom cleanliness and safety protocols

Qualifications:

• High school diploma or equivalent
• preferred experience in manufacturing, inspection, assembly, or FDA/ISO practices
• basic computer skills
• ability to interpret manufacturing instructions and operate microscopes
• availability for standard shifts plus OT and weekends

Additional information:

High-value biopharma specifics include involvement in cardiac medical devices, quality-driven manufacturing, and cleanroom GMP compliance. Collaboration likely with quality, production, and engineering teams, though not explicitly stated. Work setup is in a cleanroom environment with standing and lifting requirements, primarily Monday to Friday with overtime. The role emphasizes precision, quality, and adherence to regulatory standards pertinent to medical device production.