Associate, Site Quality Operations

Quality Operations SpecialistResponsible for the execution of shop floor Quality Operations activities at the facility. Responsible for ensuring compliance with the Quality Management System through execution of company Standard Operating Procedures (SOPs), Operations Work Instructions (OWIs), and application of current Good Manufacturing Practices (cGMP) to the ongoing operational activities.This position includes multiple levels, with scope, independence, and complexity of work increasing based on demonstrated skills, experience, and sustained performance.Key Responsibilities:Daily shop floor execution of site quality activities at the facility including but not limited to Incoming Inspections, In-Process Quality Checks, Line Clearances, and Returns Processing.Complete cGMP documentation as required to maintain compliance with the QMS.Complete in-process inspections/checks outlined in SOPs and OWIs.Support Investigations, and Corrective and Preventive Action (CAPA) implementation at the Facility.Execute shop floor level documentation for all defective, damaged, or returned materials until final disposition.Support CAPA Effectiveness checks as assigned by Quality LeadershipPeriodic review of housekeeping issues and records on floor and warehouse.Perform other assignments as required by Quality Leadership.The above duties are meant to be representative of the position and not all-inclusive.Minimum Job Requirements:Education/Training:High School Education. Healthcare warehouse experience a plus.Depending on role, quality experience in health care or healthcare-related fields is preferred. Entry level with limited experience may be considered.Knowledge, Skills & Abilities:Ability to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions and decimals.Ability to compute rate, ratio and percent.Ability to work with limited supervision at the direction of Quality LeadershipWorking knowledge of current Good Manufacturing Practices.Microsoft Office products. Proficient in use of computers and ability to learn internal software programs as applicable.cGMP Documentation Practices (preferred)Physical Demands:Ability to stand and walk for extended periods while performing inspections and supporting warehouse and production activities.Ability to frequently bend, stoop, reach, and move throughout warehouse and operational areas.Ability to lift and/or move materials or equipment up to 25 pounds, and occasionally up to 40 pounds, with or without reasonable accommodation.Ability to use hands and fingers for handling documents, operating computers, and performing detailed inspections.Ability to visually inspect materials, labels, and documentation, including close vision and attention to detail.Ability to work in a warehouse or manufacturing environment with varying temperatures, noise levels, and proximity to moving equipment.Ability to sit for periods of time while completing documentation, reviewing records, and using office equipment.Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.The expected base pay range for this position is $23-25/hr. The actual compensation for the position may vary based on market differences and on factors such as skills, experience, qualifications and can vary based on location and/or work schedule. In addition to base pay, CareTria offers a comprehensive benefits package. Full-Time benefits include access to health, dental, and vision insurance; retirement plan options; paid time off; paid parental leave; employee assistance programs; and other perks. Eligible employees may also have access to performance bonuses.CareTria is an Equal Opportunity Employer.