Leads multiple project activities throughout project lifecycles to ensure completion within the defined scope, quality, time and cost constraints.
Work closely with cross-functional teams, and assigned project managers to plan and develop scope, deliverables, required resources, work plan, budget, and timing for new initiative.
Develop and control deadlines, budgets and activities.
Apply change, risk and resource management.
Resolve projects’ higher scope issues.
Assess program strengths and identify areas for improvement.
Ensure goals are met in areas including customer satisfaction and team member performance.
Implement and manage changes and interventions to ensure project goals are achieved.
Meeting with stakeholders to make communication easy and transparent regarding project issues and decisions on services.
Producing accurate and timely reporting of program status throughout its life cycle.
Analyzing program risk.
Preparation/update, review and/or approval of validation protocols and reports for sterilization processes within Convatec sites.
Requirements
At least 3 years of project management experience in manufacturing operations.
Good understanding of medical device sterilization validation and processes.
Must be a team player able to work in a fast-paced environment with demonstrated ability to handle multiple competing tasks and demands.
Strong organization, planning and time management skills to achieve results.
Strong personal and professional ethical values and integrity.
Strong interpersonal & collaboration skills to work effectively with all levels of the organization including suppliers and/or external customers.
Proficient Project Management Skills
Proficient computer skills: MS Office (Outlook, PowerPoint, Word, and Excel), Microsoft Teams, and Adobe Acrobat Pro.
Quality System experience from Medical Device, IVD or Pharma background.
Experience in microbiology or sterilization techniques and processes.
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