Request
(MP) ATOS Netherlands BV
Labeling Change Manager (Medical device labeling) - 1122367
Labeling Change Manager (Medical device Labeling) - 1122367
Info
Function
Labeling Change Manager (Medical device Labeling) - 1122367Location
LeidenHours per week
40 hours per weekDuration
15.07.2025 - 31.12.2025Application number
SRQ176932Segment
ICT | (Atos) Development, Software Design & DevOpsClosing date
10.07.2025
12:00
Role description and task arrangements
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
Company data
Company data
(MP) ATOS Netherlands BV
Role description and task arrangements
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
Share this application
Place your bid on Striive
https://login.striive.com/For this assignment you need to place a bid on Striive. Striive is the largest assignment platform in the Benelux where more than 20,000 assignments are published annually.