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Summary:
This role is responsible to supervising the team responsible for handling of complaints across various products, following the applicable regulations and procedures. This role oversees and is responsible for the team’s activities and KPI’s. This role demonstrates effectiveness in tasks completion, decision-making, empowerment of others, problem solving and team leadership. A functional understanding of FDA, ISO and Baxter Quality systems is also required.
Essential Duties and Responsibilities:
Serves as a Subject Matter Expert for PostMarket surveillance processesSupervising employees to ensure achievement of operational goals and KPIs, and ensuring team adherence to established processes and regulationsManaging daily work assignments for the team and distributing daily assignments to the team, to ensure on time complaint processing, regulatory reportability determination, and reportingCreating and/or analyzing operations metrics and reports to identify improvement opportunitiesOverseeing and providing regular updates and reports on team performance and key metrics to managementIdentifying and escalating issues as appropriate; ensuring Postmarket Surveillance leadership is informed of high risk issues in a timely manner. Participating in resolution of escalated issues and risks, as assignedLeading and/or participating in cross functional continuous improvement activities and projects, including NCRs/CAPAsParticipating in audit readiness activities and efforts for Postmarket Surveillance functionParticipating in external and internal Audits as a complaint process Subject Matter Expert, including direct interactions with the Auditor(s), providing support to Audit requests, as neededMaintaining a high level of expertise in current regulatory requirementsPerforming Post Market Surveillance tasks as assigned by line managerQualifications:
Ability to effectively communicate (verbal and written) across different functions and across multiple levels within the organizationAbility to effectively lead a team, motivate and influenceStrong understanding of complaint process and regulatory reporting regulations applicable to Baxter products (medical devices, pharmaceuticals, etc.)Strong critical thinking and problem solving skillsAbility to drive decisions and actions quickly and effectivelyAbility to make independent decisionsAbility to deal with ambiguityCollaboration and TeamworkDetail OrientedCustomer FocusStrong technical writing skillsEducation and/or Experience:
Bachelor’s degree (Science or Engineering preferred)5-8 years of experience in Quality, or related field in the medical products industryExperience with leading people (directly or indirectly through project teams)Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Reasonable Accommodations
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