Quality Control Inspector II – Medical Devices (Onsite)

Tandem Diabetes Care, Inc.; Irvine (CA); On-site; USD 37,000 - 41,000; Full time

Job summary

Tandem Diabetes Care, Inc. in Irvine, California, is seeking a Quality Control Inspector II for on-site testing and inspections of raw materials, sub-assemblies, and finished products. You will support development, quality, and manufacturing teams with lab testing, documentation, and calibration activities.

The role requires a 4+ year QC inspection background, knowledge of QSRs and cGMP, and strong documentation skills. This temporary on-site position offers day shift hours and onsite training.

Qualifications

• Knowledgeable with QSRs.
• Must have strong cGMP documentation skills.
• Working knowledge of small scale electromechanical device assembly operation.
• Ability to effectively share information regarding issues in written or verbal form and making recommendations in a clear and concise manner.
• Proficient with Microsoft Office and Internet.
• HS Diploma or equivalent required, with some post high school technical training preferred.

Responsibilities

• Performs inspections on raw materials and sub-assemblies to identify non-conforming material.
• Performs testing on prototype and production product to support Product Development, Quality, and Manufacturing Technology engineers.
• Maintains calibration and preventive maintenance records for inspection equipment.
• Documents work on appropriate forms as required by test protocols and SOPs.
• Tests components, in-process, and finished product independently following established SOPs and WIs.
• Complies with safety and operating policies and procedures.

Skills

QSRs knowledge

cGMP documentation

Electromechanical assembly

Written/verbal communication

Teamwork

Prioritization

MS Office

Education

HS Diploma or equivalent

Job description

Tandem Diabetes Care, Inc. in Irvine, California, is seeking a Quality Control Inspector II for on-site testing and inspections of raw materials, sub-assemblies, and finished products. You will support development, quality, and manufacturing teams with lab testing, documentation, and calibration activities.

The role requires a 4+ year QC inspection background, knowledge of QSRs and cGMP, and strong documentation skills. This temporary on-site position offers day shift hours and onsite training.