QA Tech - 2nd Shift

SRI Healthcare, LLC • Chattanooga, TN

1d • Onsite

About The Position

SRI Healthcare, LLC, a Subsidiary of NOVO Health Services offers a healthcare service that provides a total and unique opportunity for hospitals to source their Sustainable Reusable Sterile Packs as well as other sustainable healthcare linens such as DermaTherapy®, Isolation Gowns, Sterilization Wrap, and cubicle/privacy curtains. SRI's products and services help Healthcare providers attain their sustainability goals, improve surgeon and staff satisfaction while ensuring continuity of supply. SRI operates three regional processing facilities located in Raleigh, NC, Chattanooga, TN, and Mason, OH. Our state-of-the-art, FDA-regulated service centers provide daily processing, assembly, and delivery of reusable products required for surgery. SRI is the only “one stop shop” service provider in U.S. currently serving all healthcare-related end markets with Sterilized Reusable Surgical Solutions. Get to know us: SRI Health Care, with headquarters in Atlanta, GA, offers linen management solutions to the healthcare industry. SRI keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs. SRI’s wide range of service programs offer a variety of options to provide a seamless, single source distribution system. SRI’s regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes. SRI Health Care is the only “one stop shop” service provider in U.S. currently serving all healthcare-related end markets with both Healthcare Laundry Services as well as Sterilized Reusable Surgical Solutions.

Requirements

• Must be detailed-oriented.
• Verbal ability to assertively interact with all levels of personnel including senior management on quality matters.
• Ability to manage time and work with minimal supervision
• Well organized with ability to maintain precise records.
• Knowledge of computer programs, word processing and spreadsheet
• Excellent written communication skills
• Flexible in work hours.
• Ability to communicate effectively with supervisors and coworkers.
• Ability to read and understand applicable Standard Operating Procedures

Responsibilities

• Ensure quality control functions are performed according to written Standard Operating Procedures and GMP.
• Assist with the facility training of employees, annual updates and other required instruction as needed. Programs include but are not limited to, blood borne pathogens, lock-out tag-out, right to know and evacuation procedures.
• Assist with the maintenance of the Medical Device Records log; distribution and control of all related documents.
• Maintain sterility release records and coordinate release of individual loads and disposable accessory packs.
• Assist with the product complaint program as directed by the Q. A. Supervisor.
• Responsible for in-process inspections, instrument inspection, dispositioning of components and product audits as directed by the Q. A. Supervisor.
• Audit job performances to ensure SOP/GMP compliance.
• Assist with bio-burden and airborne environmental sampling.
• Other duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED