Regulatory Affairs Project Specialist - System Implementation

Detalles de la oferta

.Ecolab, Purolite Resins, the world leader in resin-based separation, purification and extraction technology, is seeking a Senior Regulatory Affairs Specialist .We manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It's an exciting business which helps make the world cleaner, safer and healthier.Are you passionate about regulatory compliance, business growth and project management? We are looking for a dynamic Senior Regulatory Affairs Specialist to lead our BPT divisional Regulatory business readiness activities for the SAP Global implementation. This is a fantastic opportunity to make a significant impact on our organization by ensuring compliance with all relevant regulatory requirements and standards.What's in it For You:The opportunity to take on some of the world's most meaningful challenges, helping customers achieve clean water, safe food, abundant energy and healthy environments.The ability to make an impact and shape your career with a company that is passionate about growth.The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best.Why choose Ecolab?A world-leading international organization, benefitting from a diverse, multinational team.A fast-paced, dynamic, and rapidly growing environment.Manufacture of high-quality technical products, developed hand-in-hand with leading minds in the industry.Entrepreneurial workplace culture with a flat management structure, encouraging new approaches and ideas.What You'll Do:Lead the Regulatory business readiness activities for SAP Global implementation.Work with Regulatory teams, such as Product Safety, Transport Classification, and Registration & Approvals during SAP EHS implementation to ensure processes comply with all relevant regulatory requirements and standards.Lead in setting up processes within SAP/specification system for highly regulated Pharma products, including Active Pharmaceutical Ingredients (API).Manage and coordinate project activities to ensure timely and successful implementation.Collaborate with cross-functional teams to align regulatory strategies with business objectives.Monitor and report on project progress, identifying and mitigating risks as necessary.Provide regulatory guidance and support to project teams throughout the implementation process.Partner with various functions such as the Specification team, Quality, Marketing, Supply Chain, and others to identify processes and appropriate review steps for SAP implementation.What you'll need:Master's degree in relevant fields.Proficiency in English (written and oral).Ability to analyze regulatory data and provide actionable insights.Strong project management and problem-solving skills to address project challenges


Salario Nominal: A convenir

Fuente: Jobtome_Ppc

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