BE PART OF SOMETHING NEW—AND MAKE IT MATTER.

Are you ready to launch your career in the Quality field with a company that’s building the future of pharmaceutical and medical device design and packaging? Gilero, a Sanner Company, is opening a brand-new manufacturing site focused on injection molding for life-changing products—and we’re looking for driven individuals to grow with us from day one.
As our first Quality Technician, 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, contribute to something meaningful, and have a clear path for growth within the organization.
Whether you’ve recently earned your Associate’s degree or you’re looking to transition into the medical manufacturing space, this is your chance to get in early, work hard, and build a career in Quality with a company that values integrity, precision, and people.
Location: Greensboro, NC

SKILLS/QUALIFICATIONS:

· Associates Degree.
· US Citizen or Green Card holder.
· 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.)
· Strong attention to detail, technical writing, and verbal communication skills.
· Proficient computer skills, including Excel and Word.
· Some laboratory, good documentation practices and/or quality assurance experience preferred.
· Basic understanding of good manufacturing practices and operations preferred.
· Detail-oriented with strong documentation and communication skills.
· Willingness to learn, ask questions, and take initiative.
· Ability to thrive in a fast-paced, regulated manufacturing environment.
· Interest in building a career in Quality and Medical Device Manufacturing.

· 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.