1006 United Kingdom is looking for a Sterilization Program Manager to own the development and execution of a portfolio of sterilization projects and programs. You will act as a key liaison between program teams and stakeholders, ensuring all initiatives are completed on time and within budget in a dynamic, geographically dispersed environment.
What You'll Do
- Lead multiple project activities through their full lifecycle, ensuring delivery within defined scope, quality, time, and cost constraints.
- Work closely with cross-functional teams and assigned project managers to plan and develop scope, deliverables, resources, work plans, budgets, and timing for new initiatives.
- Develop and control deadlines, budgets, and activities, applying change, risk, and resource management principles.
- Resolve higher-scope project issues and assess program strengths to identify areas for improvement.
- Ensure goals are met in areas including customer satisfaction and team member performance.
- Implement and manage changes and interventions to achieve project goals.
- Meet with stakeholders to ensure easy and transparent communication regarding project issues and decisions.
- Produce accurate and timely reporting of program status throughout its life cycle.
- Analyze program risk.
- Prepare, update, review, and/or approve validation protocols and reports for sterilization processes.
What We're Looking For
- At least 3 years of project management experience within manufacturing operations.
- A 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.
- Strong personal and professional ethical values and integrity.
- Strong interpersonal and collaboration skills to work effectively with all levels of the organization, including suppliers and external customers.
- Availability to work remotely with low supervision.
- A scientific or engineering degree in Science, Mechanical, Electronic, Industrial, or an equivalent field.
- Proficient Project Management and computer skills, including MS Office (Outlook, PowerPoint, Word, Excel), Microsoft Teams, and Adobe Acrobat Pro.
- Quality System experience from a Medical Device, IVD, or Pharma background.
- Experience in microbiology or sterilization techniques and processes.
Nice to Have
- A Master's degree.
Technical Stack
- MS Office: Outlook, PowerPoint, Word, Excel
- Microsoft Teams
- Adobe Acrobat Pro
Team & Environment
You will work with cross-functional teams and assigned project managers.
Work Mode
This is a hybrid position based in the United Kingdom.
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
