TEMP Manufacturing Tech I

TalentBurst•San Clemente, CA

5d•Onsite

About The Position

The Manufacturing Tech I contributes to the development of new designs, manufacturing processes, and other engineering and business processes from concept creation through production release. The role assembles implantable Class III ophthalmic medical devices and their insertion systems or subcomponents. Work is performed with direction from management or engineering staff, under direct oversight, and is reviewed for accuracy and content upon completion. The technician supports component inspection and cleaning, subassembly and top-level assembly fabrication and inspection, and package assembly in accordance with SOPs and DHRs, recording work as required by the quality assurance system. The role may also support engineering tests and prepare documentation for engineering test protocols and reports, validation protocols and reports, and related engineering activities. Work must help ensure products are safe and effective and meet worldwide quality, regulatory, and marketing requirements. Additional duties and projects may be assigned to support Production, Engineering, Clinical, and Quality Assurance goals. This is a three-month temporary-to-hire position in San Clemente, California, on the first shift from 6:30 AM to 2:30 PM. The listed pay rate is $20.25 per hour.

Requirements

For Level I: 0–3 years of engineering or production technician work experience.
Medical device experience is a plus for Level I.

Responsibilities

Assemble implantable Class III ophthalmic medical devices and associated insertion systems or subcomponents.
Inspect and clean components according to SOPs and DHRs, and record work as required by the quality assurance system.
Fabricate and inspect subassemblies according to SOPs and DHRs, and document work as required.
Fabricate and inspect top-level assemblies according to SOPs and DHRs, and document work as required.
Complete package assembly activities according to SOPs and DHRs, and record work as required.
Generate or edit SOPs and DHRs to support development work.
Support engineering testing by executing test methods with a level of definition appropriate to the technician level.
Prepare documentation required by engineering test protocols and reports, validation protocols and reports, and associated engineering tasks.
Complete assigned work to support safe and effective products that meet worldwide quality, regulatory, and marketing requirements.
Perform other assigned duties and projects that support Production, Engineering, Clinical, and Quality Assurance goals.