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Job Description
Job Summary: Evaluate and standardize labeling across product lines, collaborating with specialists to refine solutions and drive innovation.
Job Description:
- Evaluate content to establish standardized labels across product lines and families.
- Analyse and implement a consistent approach to template and labelling design/execution in a component content management platform.
- Create and execute solutions, including content and format analysis of existing label designs.
- Evaluate risk assessment and proposed solutions based on redlines.
- Identify issues and risks associated with proposed design.
- Apply technical expertise and perspective to simplify proposed labeling designs.
- Identify, define and implement process improvements to enhance solutions.
- Collaborate with Labelling Specialist and change initiator to refine solution requirements.
- Develop standard label templates and labelling content with the Global Labelling Systems.
- Create and update related Global Labelling Standards, Procedures, Step guides, and Training materials.
Key Responsibilities:
- Work with different suppliers and vendors to propose improvement opportunities.
- Organise label stocks inventory within global labeling team and with suppliers.
- Provide training and coaching to new labeling designers.
Requirements:
- Bachelor's Degree in a related field.
- Related experience in Labeling.
- Proven successful project management leadership skills.
- Proven expertise in Microsoft Office Suite and related tools and systems.
- Excellent problem-solving, organizational, analytical and critical thinking skills.
- Excellent written and verbal communication skills and interpersonal relationship skills.
- Ability to build productive relationships, influence others and deliver effectively in ambiguous situations.
- Good leadership skills.
- Experience managing tasks of projects.
- Moderate understanding of domestic and global development and implementation of labeling.
- Moderate understanding of medical and/or pharmaceutical regulations and standards.
- Moderate knowledge of Edwards standards and FDA regulations in relations to labeling and documentation.
- Moderate knowledge of medical device documentation development activities.
- Knowledge of ECR and PDM processes.
- Strict attention to detail.