Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit our website.About the roleEnsure the appropriate planning including key performance indicators, scope, budget, forecast, resources, identify project risks are well handled to good implementation of the change-projects in SEG.Key responsibilitiesLeads multiple project activities throughout project life cycle to ensure completion within the defined scope, quality, time, and cost constraints.Ensure appropriate management of the following change projects, but not limited: Product development project. Changes made to process and products (customer configurations).Control of project deadlines, budgets and manage activities.Create CCR documentation, when needed (be owner).Ensure the documentation of process or product changes made follow current regulations.Comply with safety, health and environmental policy, procedures established by the EHSMS.Participate in committees, trainings, and awareness, to ensure proper competency of their position if applicable.Help drive continuous performance improvement in EHS areas, recommending potential improvements to responsible management.RequirementsBachelor's degree in Business, Science and/or Engineering (or equivalent).Work experience with Project and Portfolio Management, scoping, planning, budgeting, stakeholder management and risk management (Required).Knowledge of requirements of FDA's QSR, GMP and ISO 13485 or similar regulations.Understanding / awareness of EU Regulation of Medical Devices 2017/745 (desirable).Ability to communicate effectively in English (verbal and written) is essential.#J-18808-Ljbffr