Contractor QC Technician – Medical Devices

Automatic Data Processing, Inc.; California; Presencial; USD 34.000 - 40.000; A tiempo parcial

Descripción de la vacante

INOVIO Pharmaceuticals, Inc. is seeking a Temporary Quality Control Technician (Contractor) located in San Diego, CA.

The role focuses on inspection of raw materials, in-process items, and finished products, supporting RGA and NCMR processes, and ensuring compliance with quality systems. The candidate should have 2–4 years of QC experience in the medical device or biotech sector, familiarity with FDA and ISO regulations, and the ability to work with various inspection tools in a fast-paced

Formación

• AA or equivalent from two-year college or equivalent; desired but not required.
• Minimum of 2–4 years of Quality Control experience in medical device or pharmaceutical/biotech industry; knowledge of FDA and ISO regulations.
• Strong organizational, project management and communication skills; ability to work with minimal supervision in a team.

Responsabilidades

• Perform Receiving Inspection for incoming raw materials, in-process inspections and finished product inspections.
• Support the RGA process to maintain inventory accuracy.
• Perform visual and mechanical inspections using measuring equipment (caliper, micrometer, vision system, voltmeter).
• Conduct WIP and inventory transactions to ensure proper systems and physical movement.
• Review Device History Records, inspection and test results for accuracy.
• Support Corrective Action Board activities as needed.
• Inspect Work in Progress and finished goods items.
• Handle other related tasks as assigned.

Conocimientos

Quality Control

Attention to detail

Organizational skills

Project management

Communication skills

Educación

AA or equivalent

Herramientas

Caliper

Micrometer

Vision system

PCBA tester

Voltmeter

Descripción del empleo

INOVIO Pharmaceuticals, Inc. is seeking a Temporary Quality Control Technician (Contractor) located in San Diego, CA.

The role focuses on inspection of raw materials, in-process items, and finished products, supporting RGA and NCMR processes, and ensuring compliance with quality systems. The candidate should have 2–4 years of QC experience in the medical device or biotech sector, familiarity with FDA and ISO regulations, and the ability to work with various inspection tools in a fast-paced