Supervisor, Quality Assurance-3rd shift

Takeda is the leading global biotechnology company focused on serving people with rare diseases and other highly specialized conditions. We have best-in-class products available in more than 100 countries across core therapeutic areas including Hematology, Immunology, Neuroscience, Lysosomal Storage Disorders, Gastrointestinal / Internal Medicine / Endocrine and Hereditary Angioedema; a growing franchise in Oncology; and an emerging, innovative pipeline in Ophthalmics. Our employees come to work every day with a shared mission: to develop and deliver breakthrough therapies for the hundreds of millions of people in the world affected by rare diseases and other high-need conditions, and who lack effective therapies to live their lives to the fullest.Supervises a staff of QA Associates that are responsible for providing Quality Assurance support for Fractionation manufacturing process. Provides Quality oversight of operation activities, review batch related document will use of Electronic Batch Management (EBM) system. Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Takeda quality practices Interacts frequently with functional peer, and provide coaching, training and development of subordinates. The incumbent will be responsible to handle multiple projects, demonstrate effectiveness in task completion, decision-making, empowerment of others, exception management, training, problem solving and team leadership. This position is a third shift positionlDuties and Responsibilities: Plans and schedules the work of QA Associates.Support supervision for the floor coverage (as needed) and lead daily departmental operations.Supervises a staff of QA Associates to ensure compliance with manufacturing procedures are followed on the floor.Supervising the staff to ensure that production records are reviewed established targets.Provide Training and coaching for the departmentWork closely with Production Supervision, Other QA Operations Groups, Quality Systems, and Engineering to ensure adequacy and appropriateness of product specifications.Provide support towards engineering runs and validation activities. . Review electronic batch records, identify nonconformances and participate in investigation and Corrective and Prevention Action(CAPA) activitiesProvide training and coaching to local employees and others as needed on relevant area(s). Write, review, revise, and approve written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.Oversee review and audit of various reports (Protocols, Qualifications, Regulatory Submissions, etc.)Participate in QA multi-site projects in the role of contributor, coordinator or lead.Other duties, tasks or projects as assigned.Working Environment:Will be spending large portion of time in clean room environment to provide oversight to manufacturing operations and will be required to meet applicable gowning and personal protective equipment guidelines. May be required to work weekends, evenings, off-hours, and extended periods of time.May be required to travel to local and international work locations for extended periods of time for training.Qualifications:Education and/or ExperienceBachelors degree in Engineering, Science or related field or equivalent. Minimum of 4 years of QA experience in the life sciences and experience with a medical device / pharmaceutical or other similarly regulated industry preferred.Strong interpersonal/communication/influencing/negotiation skillsStrong analytical and problem solving skills.Must have the ability to encourage teamwork and drive decisions.Must be able to handle multiple projects concurrently.Requires scientific and technical knowledge in the areas of manufacturing, laboratory testing, documentation and regulationsMust have adequate computer experience (knowledge of Microsoft Word, Excel and PowerPoint requiredKnowledge of Electronic Quality Systems( TrackWise), Process control systems (Delta V, BAS) and Electronic Batch Record Management preferred Must have knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices.

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