Quality Technician (Cooper City, FL, US, 33330)

Steris Corporation•Cooper City, FL

53d•$19 - $22•Onsite

About The Position

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. Position Summary The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. You will support manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. This is a day shift position; Mon-Fri, 9am - 6pm.

Requirements

Minimum of three (3) years of experience in a manufacturing or repair environment or other technical production tasks with a high school diploma or equivalent.
Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks with an associate degree.
Familiarity working with and using a microscope.
Experience working with a Quality Management System (ISO 13485).
Experience using basic hand tools i.e., utility knife, screwdrivers, hammers.
Proficiency using MS Office including Work, Excel and Outlook.
High level of professionalism, good communication skills, able to work individually and as part of a team.

Nice To Haves

Knowledge of metrology (mics, calipers, gauges). Ability to sit and stand for long periods of time.

Responsibilities

Assist in production line Quality investigations and associated problem-solving activities.
Will coordinate and conduct in-process and final QC product acceptance testing, depending on facility.
Investigates production line stoppages to identify corrective actions.
Participates on a Material Review Board to review and process non-conformance reports.
Enters and retrieves Quality data from local and global systems.
Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release.
Complete other duties as assigned.