Regulatory Affairs Project Manager – Regulation 1107/2009NonStop Consulting
hace 2 semanas
Regulatory Affairs Project Manager Introduction Our client is seeking a highly skilled and motivated Regulatory Affairs Project Manager to join their dynamic team. This role offers the opportunity to work at the forefront of regulatory science, contributing to the successful registration and market approval of active substances under EU Regulation 1107/2009 . The ideal candidate will have 5 to 10 years of experience in this field and a solid background in risk assessment . Why Join Our Client? Our client is a leading consulting company specializing in comprehensive registration services for the chemical industry across Europe and beyond. The company has a strong reputation for professionalism, adaptability, and delivering high-quality results. By joining our client, you will become part of a globally recognized group known for its extensive expertise in regulatory and scientific matters. The company offers a flexible working environment with options to work from various office locations across Europe or remotely from home. You will be working with a team of 50 regulatory professionals, including scientific experts, backed by the larger group of over 600 professionals worldwide. This role not only provides the chance to enhance your skills and grow within the industry but also to make a significant impact on the safety and efficacy of plant protection products. Key Responsibilities Lead and manage regulatory projects for the registration of active substances under EU Regulation 1107/2009. Prepare and review regulatory submissions, ensuring compliance with EU regulatory requirements. Conduct data gap analyses, prepare dossiers, and perform risk assessments. Liaise with clients, regulatory authorities, and internal teams to address regulatory requests and issues. Provide strategic advice and develop regulatory strategies to facilitate product registration and market entry. Ensure timely and accurate submission of regulatory documents and maintain up-to-date knowledge of relevant regulations and guidelines. Coordinate with project managers and senior specialists to deliver high-quality regulatory support and documentation. Key Requirements 5 to 10 years of experience in regulatory affairs related to EU Regulation 1107/2009, with a focus on the registration of active substances. Strong background in risk assessment for any section of the regulatory dossier. Proven experience in preparing and submitting regulatory dossiers for active substances. Excellent knowledge of EU regulatory requirements and guidelines for plant protection products. Strong project management skills with the ability to lead and manage multiple projects simultaneously. Excellent communication and interpersonal skills, with the ability to work effectively with clients, regulatory authorities, and team members. A degree in a relevant scientific discipline (e.g., chemistry, biology, environmental science). Additional Information This role offers a competitive salary and benefits package, along with the opportunity for professional growth and development within a leading global consulting group. Our client values diversity and inclusion and is committed to creating a supportive and collaborative work environment. 💌 Apply now to take the next step in your career with a leading consulting company that values expertise, innovation, and quality Send your CV to c.bonvento@nonstop-recruitment.com 💌
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spain NonStop Consulting A tiempo completoRegulatory Affairs Project Manager Introduction Our client is seeking a highly skilled and motivated Regulatory Affairs Project Manager to join their dynamic team. This role offers the opportunity to work at the forefront of regulatory science, contributing to the successful registration and market approval of active substances under EU Regulation 1107/2009...
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Regulatory Affairs Project ManagerNonStop Consulting
hace 2 semanas
spain NonStop Consulting A tiempo completoRegulatory Affairs Project Manager Location: Remote/Home Working EU Wide Introduction Our client is seeking a highly skilled and motivated Regulatory Affairs Project Manager to join their dynamic team. This role offers the opportunity to work at the forefront of regulatory science, contributing to the successful registration and market approval of active...
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Spain PQE Group A tiempo completoAre you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation...
