Quality Associate II - Onsite Weekdays

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride. Your role at Baxter The Compliance & Records Management, QAII is responsible for site QA Compliance, Internal/External Audits, Site Audit Readiness and all aspects of hosting Audits, Regulatory Intelligence (GOC), Management of the Global Entity review and Periodic Review processes, QA site Model, and other Quality System items as assigned. Main responsibilities include ensuring compliance with Regulations and corporate processes. Additional responsibilities related to Records Management include serving as the Site Records Management Coordinator and Subject Matter Expert. Important: This position is located in Medina, NY and is designed as an onsite role, with an encouraged presence of five (4) days per week to foster collaboration, innovation, and connection across the team. Baxter is seeking candidates who reside within a reasonable commuting distance and are able to regularly support the business through in-person engagement and partnership at the Medina site. What You'll Be Doing This position’s primary responsibility is ensuring compliance with Regulations and corporate processes such that desired business results are achieved. Develop and sustain the Quality Management System in line with the required regulatory and industry standards (ISO 13485) and business requirements. Understand and ensure conformance to regulations per FDA Quality System Regulation (21CFR Part 820), ISO 13485:2016, Canadian Medical Devices Regulations SOR/98-282, as well as Baxter Global Policies and Procedures applicable to elements of the Quality System. Manage site certifications, external registration requirements. Liaise with external bodies on matters relating to registration. Manage various aspects of the audit lifecycle including planning, scheduling, notification, executing, hosting, issuing reports, evaluating responses, requesting clarifications, issuing and closing CA/PA’s. This may include qualification of Site internal auditors. Write, review, analyze and revise Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc. Serve as Subject Matter Expert (SME) in Quality compliance by maintaining a high level of expertise in current regulatory requirements. Provide training and coaching to local employees and others as needed on relevant area(s). When required, assist other quality areas in the successful performance of these activities. Lead Audit Readiness efforts for the site and ensures compliance to regulatory requirements. Manage the site Internal Audit Program, participate in audits and/or qualify/oversee alternate Site auditors, plans for corrective and preventive actions related to internal audit findings or gaps identified in the QMS. Manage Site Compliance programs such as Global Observation Certification, Global Entity Review, and Periodic Review Strategize quality improvement activities in collaboration with other departments. Manage activities of self in achieving defined quality goals in an efficient, accurate and timely manner. Provide detail analysis of the QMS KPIs for management review meetings and other platforms as needed. Balance cost, quality, people, and delivery objectives to meet plant goals utilizing standard enterprise management system. Ensures KPIs are met by working to overall plan, including management of, and reporting. Support in failure investigation activities (CAPA projects) to identify the root cause, develop appropriate corrective/preventive actions and approve CAPA’s, NCR’s. Other duties, tasks or projects as assigned. Records Management: Maintaining an inventory of stored Records, ensuring Records are indexed and tracked for ease in retrieval, managing Records submitted to and/or stored with third party storage suppliers and evaluating Records to determine their destruction eligibility. Maintain an inventory of stored Records Ensure Records are indexed and tracked for ease in retrieval. Ensure Records are archived/stored in appropriate locations (both electronic and physical). Track storage submissions and retrieval activities for records submitted to and/or stored with offsite storage providers. Monitor/adhere to Legal Hold Orders Annually evaluate Records to determine their destruction eligibility. Periodically (at least annually) review trigger dates to enter known dates that have occurred. Prepare and route destruction eligibility reports/lists for review by Functional Leaders Upon approval, destroy Records in a timely fashion in compliance with Baxter’s policies and procedures. Other duties, tasks or projects as assigned. What You'll Bring Bachelor’s degree required. MS in science/engineering a plus. Minimum of 3+ years of experience in Quality with emphasis on oversight of regulation and compliance, or related field with a medical device/pharmaceutical company or similar regulated industry, preferred. Must be experienced with interpreting quality system regulations. Audit experience is preferred. Working knowledge of Quality Systems and related requirements and standards, including 21 CFR Part 820, ISO 13485, preferred. Knowledge of risk management, root cause analysis, corrective and preventive action and document control. Demonstrated use of quality and root cause analysis tools, principles, and methodologies including statistical tools. Proficient with computers and in the use of Microsoft Office Suite. Strong verbal / written communication skills, problem solving and personal conflict resolution skills. Strong attention to detail with the ability to independently organize workload, perform under strict deadlines and changing priorities with minimal supervision. Project management skills and must be able to handle multiple projects concurrently. Ability to communicate with all levels within the organization. Able to demonstrate responsiveness to customer needs, within job scope. Knowledge of Food & Drug Administration (FDA) Regulations and application of Good Manufacturing Practices. Comprehension of design methodology, product configuration and complex manufacturing processes. Ability to excel in a team-oriented environment. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. While performing the duties of this job, the employee: Must be able to sit, stand, bend, stretch and walk throughout the workday. Must