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A leading global medical technology firm in the UK is seeking an Automation Project Coordinator to manage multiple projects for efficiency and regulatory compliance. The ideal candidate will have strong project management skills, ensuring projects are delivered on time and within budget. Excellent communication and collaboration skills are essential as the role involves coordinating with various departments. This position offers hybrid working options.
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Position Overview:
The Project Lead will support the Project Manager(s) in delivering various project types (productivity, material changes, and resilience projects).
The Project Lead will be responsible for managing multiple projects, which will vary depending on the complexity of the change.
Key Responsibilities:
Develop and maintain detailed project plans, clearly identifying and sequencing all activities required for successful and timely project delivery.
Assess and define the necessary resources (time, budget, equipment) to support project execution.
Establish and manage a communication plan to keep stakeholders informed of project progress, risks, and key milestones.
Monitor project budgets and track spend against allocated resources, ensuring financial control across all initiatives.
Regularly review and update project plans, escalating risks or delays to senior management as appropriate.
Ensure full compliance with the Convatec Quality Management System, adhering to all relevant SOPs and regulatory requirements.
Evaluate project outcomes against defined objectives, incorporating lessons learned to drive continuous improvement.
Follow established project management processes and tools while proactively identifying opportunities to streamline and enhance ways of working.
Act as Change Owner, preparing and presenting change proposals to the Governance Board for review and approval.
Lead the preparation and submission of Change Control Records (CCRs), ensuring alignment and approval from all relevant functions.
Maintain a decision register and ensure accountability across the project team and leadership, driving the timely resolution of key decisions
Authority:
The Project Lead is responsible for approving Change Control Records in the Trackwise system as the owner of the change.
The Project Lead will approve various documents through the project lifecycle (examples, validation documents, design documents, Non-Standard Production Requests)
Skills & Experience:
Managing complex projects, adhering to timelines and budgets.
Understanding of regulatory compliance and good documentation practices.
Collaborating closely with subject matter experts across multiple functions and locations.
Understanding of Project Management principles and translating plans into actions.
Demonstrating values and behaviours supporting the Convatec ‘Forever Caring’ Promise.
Excellent interpersonal and communication skills, with the ability to build relationships.
Results-oriented and solution-oriented, focusing on meeting targets and deadlines.
Understanding of financial principles and allocation of resources to support project delivery.
Effectively communicating to a diverse audience using various formats with clear and logical output (presentations, emails, leading meetings, face-to-face, etc.).
Working independently, dealing with ambiguity, and translating it into clear, actionable steps.
Navigating project models such as stage gate processes.
An understanding of Medical Device Regulations and experience with Design Control is desirable.
Qualifications/Education:
Prince 2 Practitioner or a Project Management Professional (PMP) qualification is desired.
Dimensions:
Indirect Reports - Leading a team and coordinating cross-functional areas and business functions.
Principal Contacts & Purpose of Contact
You will work extensively across the business with various stakeholder groups, including but not limited to:
Automation Managers – Working with the automation managers to assess priorities and resources of individual projects.
Operations / Supply Chain - The planning and securing of manufacturing line time and understanding stock levels.
R&D – Reviewing the impact of the change on the design requirements and understanding if the change is feasible.
Regulatory – Ensuring compliance with the Regulatory Bodies and impact on the markets for changes made to a device.
Engineers – Reviewing the impact of the change on the validated state of the equipment, using the engineering team to make the technical decisions for each project.
Finance – Securing budget and tracking spend through the project life cycle.
Quality – Various quality departments from Product Quality Engineers to manage risk, Supplier Quality for onboarding new suppliers, and Change Control Specialist.
External Suppliers – Lead meetings with the suppliers with support from the Automation Managers.
Travel Requirements
Travel may be required with this role (15%), including to other Convatec manufacturing facilities and to supplier facilities as required. This could be domestic or international travel.
Working Conditions
Hybrid working (as agreed with the line manager)
Or remote for the right candidate.
Special Factors
There will be collaboration across international timelines, which may result in some work requirements outside of normal office hours.
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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.
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