Quality Associate

Job Summary Quality Associate at a premier pharmaceutical company in Bloomington, IN. Salary $33/hr Responsibilities Administrating the Supplier Quality Management (SQM) documentation within the eQMS system and Simtra SQM SharePoint, reporting to the Senior Manager, Supplier Quality. Collaborating with Supplier Auditors in maintaining Quality Agreements and ensuring compliance with local and global procedures. Collecting and analyzing SQM system metrics and assisting in the creation of metric presentations for Management Meetings. Qualifications Hold a Bachelor's degree (preferred) and have a strong understanding of cGMPs and other regulatory guidelines applicable to the life science industry. Possess computer proficiency in Microsoft Word, Excel, and Outlook, along with the ability to use enterprise software such as JDE, D365, Trackwise, or Veeva. Have experience in data collection and be willing to work overtime, including nights and weekends, as needed. Equal Employment Opportunity Statement Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. #J-18808-Ljbffr