Quality Systems Associate

Quality Systems Associate Under the direct supervision of the Quality Systems Manager, perform quality assurance and training functions to ensure compliance with internal and external regulations and protocol. Primary Responsibilities Complete weekly review of equipment QC and maintenance records. Document, investigate, and perform root‑cause analysis for deviations and customer complaints, specifically relating to product quality and/or donor safety. Inspect and release incoming supplies; investigate and report supplies that have not met quality specifications and requirements prior to use. Perform documentation review for unsuitable test results. Assist the Quality Systems Manager to ensure that cGMP regulation, SOPs, and regulatory requirements are followed. Perform all product release activities. Review lookback information and documentation. Review waste shipment documentation. Review unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process. Review electronic donor chart exceptions impacting donor eligibility/safety and/or product quality. Review donor deferral notifications from competitor centers. Review plasma processing documentation to ensure the proper freezing, storage, and handling of product. Assure center training programs follow procedural requirements as defined in the donor center SOP and/or training program documents. Create, maintain, and audit training records and files to ensure compliance. Perform employee training observations to ensure staff competency prior to releasing employees to work independently. Conduct required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations. When the Quality Systems Manager is absent, review and approve deferred donor reinstatement activities. Assist with completion of the internal donor center audit. Perform review of monthly trending report. Perform review of donor adverse events reports and applicable related documentation. Conduct training to address donor center corrective and preventative measures. Additional Responsibilities Maintain certification as a Donor Center Technician. Knowledge, Skills, and Abilities Developing command of interpersonal communication, organizational, and problem‑solving skills. Ability to understand FDA regulations. Strong integrity and commitment to quality and compliance. Good knowledge of mathematics. Legible handwriting. Proficiency with computers. Ability to work flexible scheduling to meet business needs. Perform basic document review and employee observations. Communicate openly with the CQM on issues noted during reviews. Understand and follow SOPs and protocols. Perform primary responsibilities of the Quality Associate role in a proficient manner. Have a basic understanding of cGMP and quality systems. Be able to spend hours sitting and reviewing documentation for accuracy. Demonstrate good organizational skills and attention to detail. Education & Experience High school diploma or GED. Obtain state licensures or certifications if applicable. Typically requires no previous related experience. Occupational Demands Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms, electrical office and laboratory equipment, and extreme cold below 32°F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves, and cold gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position requires bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple movements of the fingers, hands, and wrists. Ability to make precise coordinated movements of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch, or sit on one's heels on rare occasions. Occasionally walks, bends, and twists at waist. Light lifting of 15 lbs with a maximum lift of 50 lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups. Compensation & Benefits The estimated pay scale for Quality Systems Associate role based in Colorado Springs, CO, is $20.40–27.60 per hour. Additionally, the position is eligible to participate in up to 5% of the company bonus pool. Benefits include Medical, Dental, Vision, life insurance, PTO, paid holidays, up to 5% 401(K) match, and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skill set, knowledge, where the role is performed, internal equity and market data. APPLICATION DEADLINE DATE = 06/22/2026 @ 12:59 AM EDT. Grifols provides equal employment opportunities to applicants and employees without regard to race, color, sex, gender identity, sexual orientation, religious practices and observances, national origin, pregnancy, childbirth, or related medical conditions, status as a protected veteran or spouse/family member of a protected veteran, or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws. #J-18808-Ljbffr