Supplier Quality Assurance Specialist

Supplier Quality Assurance SpecialistFull-timeWorkday Global Grade: 12Company DescriptionAbout AbbVieAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.Job DescriptionComplianceManage low risk investigations arising from materials nonconformity with cross functional teamManage low risk supplier change control with cross functional teamSupport performance measurements of the Supplier Quality Management business processesManage Site CAPA systems and support monitoring programCoordinate site supplier quality issues (such as deviations), audit assessments and subsequent follow-up actionsEnsure compliance with applicable AbbVie policies, processes and procedures, contributing to the  execution of strategies and oversight of Supplier Quality programsSupport and administration are provided timely for all supplier related quality activities to the high throughput multi-products plants with 24/7 operations while maintaining customer satisfaction service levelMaintain high levels of Customer satisfaction by positively managing internal and external relationshipsPromote and follow safety work practices in the workplaceAny other tasks as and when assigned by the Supplier Quality SupervisorOperational Excellence - Project/New Product IntroductionSupport global supplier quality team initiatives or other site improvement projects e.g. New Product IntroductionSupport cross functional projects where necessaryQualificationsBachelor’s degree in sciences (e.g. Biology, Chemistry), Pharmacy, or Engineering Degree or equivalentMinimum 2 years relevant work experience in cGMP Biotechnology/Pharmaceutical manufacturing industry is preferred.Knowledge in Supplier Quality Management and regulations is preferred.Experience in SAP, Trackwise are preferredGood communicator with experience with internal stakeholders is required.Highly Motivated, Independent, Organized and Growth mindset.Able to be a team player and collaborate with different departments and all levels of the organizationAgile and able to respond to business urgent requestsMicrosoft office skills.Additional InformationAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.htmlBy clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy applyI'm interestedI'm interestedPrivacy Notice