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DO WORK THAT MATTERSAt Abbott, diverse ideas, perspectives, and
expertise allow us to create life-changing solutions that help people live
healthier lives. In 150 countries and with businesses spanning nutrition,
diagnostics, medical devices, and branded generic pharmaceuticals, Abbott
offers you enormous opportunities to explore your interests and help you
achieve your career and personal goals.Abbott
Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses,
bringing together exceptional teams of experts and industry leading
technologies to support diagnostic testing which provides important information
for treatment and management of diseases and other conditions.The position of Supervisor,Quality Assurance is within our Infectious Disease Developed Markets
business unit located at Auburn, NY. In this role you will be responsible for
training and directing the work of direct reports in their designated
responsibilities and assisting in and/or driving the maintenance of certain
areas of the quality system and promoting quality awareness throughout the
organization.RESPONSIBILITIES:Quality Assurance ResponsibilitiesResponsible for support of product
release and product quality assurance. Review and assess from a technical
perspective the content of manufacturing, process, procedure and materials. Assure
compliance to applicable standards. Provide training, assist with collection
and analysis of relevant metrics and trending.Provide support for quality issues
and investigations, including complaint investigations.Supervisory ResponsibilitiesDirectly supervises Quality
Assurance Technicians in the Quality Assurance department. Carries out
supervisory responsibilities in accordance with the organization's policies and
applicable laws. Responsibilities include interviewing, hiring, and training
employees; planning, assigning, and directing work; appraising performance;
rewarding and disciplining employees; addressing complaints and resolving
problems.BASIC QUALIFICATIONS | EDUCATION:·
Bachelor's degree in Engineering, Chemistry, Biotechnology, Life Science or
related technical field or equivalent experience and education.·
3+ years’ experience in a medical device company in a quality or regulatory
functionPREFERRED QUALIFICATIONS:·
Prior lead or supervisory experience.COMPETENCIES:·
Working knowledge of FDA cGMPs/QSR, USDA 9CFR, CLIA, IVDD and ISO Quality
system requirements·
Demonstrated understanding of lab practicesAn Equal Opportunity EmployerAbbot welcomes and encourages diversity in our workforce.We provide reasonable accommodation to qualified individuals with disabilities.To request accommodation, please call 224-667-4913 or email corpjat@abbott.com
