Labeling Change Manager (Medical device Labeling) – 1122367 - Freelance opdracht in Zuid-Holland
(MP) ATOS Nederland BVOpdrachtomschrijving
Rolomschrijving en taakafspraken
Language: Dutch is must
Location : Leiden (resource to be working for all five days in office as per project/customer requirement and no hybrid module.)
Rate : Market rate
Labeling Lead Skills:
• Self-starter, works effectively with general direction / minimal supervision - following standardized practices & controlled procedures
• Strong communication– written, verbal and across digital mediums necessary for communicating with required stakeholders
• Experience with Design change control systems for Medical devices.
• Experience in Lifecycle product management.
• Able and willing to guide others in area of specialty
• Management 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 methodology
• Ability 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 preferred
• Project Management Certification preferred
Location : Leiden (resource to be working for all five days in office as per project/customer requirement and no hybrid module.)
Rate : Market rate
Labeling Lead Skills:
• Self-starter, works effectively with general direction / minimal supervision - following standardized practices & controlled procedures
• Strong communication– written, verbal and across digital mediums necessary for communicating with required stakeholders
• Experience with Design change control systems for Medical devices.
• Experience in Lifecycle product management.
• Able and willing to guide others in area of specialty
• Management 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 methodology
• Ability 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 preferred
• Project Management Certification preferred
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