United Spinal Association Jobs

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role Under general supervisor, the scope of the Manufacturing Technician I is responsible for a variety of assembly and non-assembly functions in support of manufacturing goals. This role is located in Athens, Ohio. The Responsibilities Responsible for completing set-up operations for one or multiple of the following: assembly, packaging and prep operations in compliance with approved documentation and QSR Responsible for the completion and accuracy of documentation associated with the manufacturing processes Responsible for cleaning, performing and documenting routine equipment maintenance and minor repair Assists in Lean Initiatives, such as 5S, Zone assignments Responsible for record keeping Responsible for supporting new equipment installation and validation Carries out duties in compliance with established business policies. Perform other duties & projects as assigned. The Individual Required: High school diploma or equivalent One to two years of related experience Knowledgeable of federal and other regulations, e.g. QSR's, ISO, ISO 13485, CMDR Computer operated experience Knowledge of MS Office and manufacturing systems Experience with working with semi-automated equipment Basic knowledge of GMP, Documentation Practices Preferred: Demonstrates commitment to the development, implementation and effectiveness of Quidel Quality Management System per ISO, FDA and other regulatory agencies Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities The Key Working Relationships Internal Partners: Mechanics, Engineers and Management team The Work Environment The work environment characteristics are representative of a manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines. Position requires ability to lift up to 50 lbs. on a regular basis. May be required to perform repetitive manufacturing processes (e.g., manual lamination, manual cassette assembly, pouch inspection, etc.) up to 90% of workday. Walking, standing, and/or sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted. Equal Employment Opportunity QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, s