Description:Labeling Lead Skills:Self-starter, works effectively with general direction / minimal supervision - following standardized practices & controlled proceduresStrong communication– written, verbal and across digital mediums necessary for communicating with required stakeholdersExperience with Design change control systems for Medical devices.Experience in Lifecycle product management.Able and willing to guide others in area of specialtyManagement of multiple projects with aggressive project deadlines and schedules.6-8 years’ experience with at least 3 years’ experience related directly to the development of Medical device Labeling.Familiarity with Adobe InDesign /Illustrator is a plus.Solid works, AutoCAD is a plus.Project management methodologyAbility to advocate and coach, representing the brand of the labeling COE and business processes.EDUCATION / DEGREE REQUIRED:B.S./B.E. degree or qualifying combination of education & related work experience.Experience working within a Medical Regulatory environment preferred.Experience in technical writing for regulated industries preferredProject Management Certification preferredMandatory skills:Project management methodology,Design change control systems,Product management VIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status
Description:Labeling Lead Skills:Self-starter, works effectively with general direction / minimal supervision - following standardized practices & controlled proceduresStrong communication– written, verbal and across digital mediums necessary for communicating with required stakeholdersExperience with Design change control systems for Medical devices.Experience in Lifecycle product management.Able and willing to guide others in area of specialtyManagement of multiple projects with aggressive project deadlines and schedules.6-8 years’ experience with at least 3 years’ experience related directly to the development of Medical device Labeling.Familiarity with Adobe InDesign /Illustrator is a plus.Solid works, AutoCAD is a plus.Project management methodologyAbility to advocate and coach, representing the brand of the labeling COE and business processes.EDUCATION / DEGREE REQUIRED:B.S./B.E. degree or qualifying combination of education & related work experience.Experience working within a Medical Regulatory environment preferred.Experience in technical writing for regulated industries preferredProject Management Certification preferredMandatory skills:Project management methodology,Design change control systems,Product management
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