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EMEA Regulatory Affairs Manager
Il y a 4 mois
LANXESS is a leading specialty chemicals company based in Cologne, Germany. With around 13,200 employees in 33 countries, our primary expertise lies in producing, developing and marketing chemical intermediates, additives, specialty chemicals and plastics.
LANXESS FRANCE is currently seeking a strong, motivated, and talented individuals with the appropriate regulatory and technical experience to be part of the Home & Personal Care regulatory team for the position of:
EMEA Regulatory Affairs Manager, within the Material Protection Products (MPP BU) Business Unit and Business Line CNS Consumer Solutions.
BL CNS Consumer Solution is a dynamic and fast-paced business, positioned at the forefront of disease control, home and personal care preservation, and state of the art beverage preservation.
Location: LANXESS France, or other LANXESS EU locations.
The purpose of the position is to support business compliance with regulatory authorities in the Europe, UK and the Middle East while also ensuring that the data pack of projects are up to date to comply with local requirements.
KEY RESPONSIBILITIES:
- Working in coordination with other CNS RA managers to follow home & personal care products registration & renewal under BPR.
- Defining with manager RA projects targets and follow completion. Coordinating the activities of the biocides group, to ensure a structured work program and clear goals and targets.
- Developing technical master dossiers and technical materials supporting product registrations (includes development of BPR also producing data to support non EU BPR product authorization dossiers), with interaction and in partnership with other functions.
- Giving clear direction, support and guidance to Biocides team to ensure delivery of the team goals.
- Facilitating relationships with regulatory agencies, including representing the company in meetings of the various professional bodies and in expert networks (B4E, EFfCI…) in order to defend Lanxess' interests in the development of biocidal products and cosmetic preservative standards.
- Anticipating regulatory developments in order to introduce into the development process the changes made necessary by new requirements.
- Ensuring compliance of the products within the BL CNS business to regulations on advertising, packaging, and advertising media and documentation.
- Providing operational support to all internal departments in order to be the guarantor of the proper application of regulatory protocols, with continued concern for compliance with quality and safety requirements when placing products on the market.
REQUIREMENTS:
- A minimum of 5 years’ experience working on the preparation of product dossiers under EU BPR.
- Master degree or higher in a physical science or related field.
- Detailed knowledge of regulatory requirements in the field of biocides.
- Competent technical and scientific skills.
- Good communications skills, including an ability to succinctly summarize to audiences of varying technical capabilities.
- Self-motivated and organized; capable of effectively managing and prioritizing a busy personal workload.
- Proven and strong problem solving capabilities.
- Ability to work in an international team.
- Fluent English and French
- Occasional overseas travel is expected.
- Encourages team spirit and promotes knowledge sharing.
For us, talent matters, and we welcome everyone who commits to our values. We strongly believe that including diverse perspectives makes us more innovative and enhances our competitiveness. Therefore, we embrace the uniqueness of every single individual and are truly committed to supporting our people in developing their individual potential.
Apply today with your full CV and we will review your application and contact you should we feel you have relevant experience.
