Quality Technician - 3rd Shift

Job Description

Job Description

Be part of something new—and make it matter.

Gilero, a Sanner Company, has opened a brand-new manufacturing site focused on injection molding for pharmaceutical and medical device packaging —and we’re looking for driven individuals to grow with us from day one. We have an opening for Quality Technician 3rd shift  that includes 3rd shift $1 differential.

You will be responsible for Quality Operations in support of development and commercial manufacturing activities. You will be on the frontlines of quality assurance, ensuring our products meet the highest standards for patients around the world. This is more than a job—it's a hands-on learning opportunity in an FDA-regulated environment where you'll gain valuable experience and contribute to something meaningful.

Whether you’ve been working in a quality role, recently earned an Associate’s degree or you’re looking to transition into a new industry, this is your chance to get in early, work hard, and build a career in Quality with a company that values integrity, innovation, collaboration, and excellence.

Responsibilities:

· Perform incoming inspection/testing and release of accepted materials.

· Perform required manufacturing line clearance activities to verify materials, labeling, and equipment prior to assembly.

· Conduct labeling verification in accordance with product requirements.

· Perform in-process testing and QA inspections, as required per product requirements.

· Support new product development projects.

· Perform environmental monitoring, including particle counts and temperature / humidity / pressure measurements. Manage controlled environment monitoring and records.

· Conduct cleaning of controlled environment areas per internal procedures.

· Support quality event initiation and investigations for nonconformance and CAPA.

· Support the calibration and maintenance process.

· Support continuous improvement projects and audits.

Skills/Qualifications:

· Associates Degree or equivalent experience.

· Familiarity with FDA/ISO/Regulatory requirements preferred.

· Basic experience with the coordination of GMP-compliant Documents, Records, and Training.

· Basic understanding of measurement tools (calipers, micrometers, etc.)