Regulatory Affairs & Safety Associate - 18 months replacement contract
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
Reckitt is seeking a dedicated Regulatory Associate, a role that sits at the core of our innovation process, ensuring that our new product developments meet global regulatory requirements with precision. You will act as a catalyst for change, using your detailed knowledge to create comprehensive dossiers crucial for product registrations. At Reckitt, every individual's contribution is key, and your role will be pivotal in navigating the intricate regulatory landscape to deliver products that enrich lives every day.
• Manage regulatory processes (registrations, variations, and renewals), ensuring timely document preparation and submission.
• Act as primary liaison with local authorities, addressing inquiries and maintaining compliance.
• Review and approve artwork and advertising materials from a regulator & medical perspective, providing improvement recommendations.
• Support uninterrupted business operations by mitigating regulatory risks and ensuring adherence to procedures.
• Collaborate closely with Marketing to develop compliant regulatory claims and contribute to brand growth.
Your responsibilities
• Taking care over regulatory procedures: new registrations, variation renewals: documents preparation, submission and handling the process
• Daily cooperation with local Authorities and handling their inquiries
• Artwork and adverts reviewing and approving them from regulatory& medical perspective, including recommendations for further improvement
• Supporting smooth business processes by preventing disruptions due to regulatory aspects
• Ensuring compliance with Regulatory procedures for all processes
• Close cooperation with Marketing Department on supporting the development of regulatory claims
• Supporting brand development from regulatory affairs perspective
• Perform tasks related to trade association activites
• Maintaining products information in relevant data bases, such as: TDS, GRAIS, CARA, Quality One, Brandwords, etc., as well as maintaining internal Regulatory administrative data bases
• Enhancing Regulatory knowledge within the team by providing learnings from own projects which are applicable to other brands and/or countries
The experience we're looking for
• Higher degree in natural sciences
• 3-5 years of experience in Regulatory Affairs in Pharmaceutical Companies; experience in Regulatory Affairs for other regulated product classes like food, medical devices, etc. will be an asset
• Fluency in Polish and English
• Understanding of the science and technology of products
• Good MS Office knowledge
• Strong ownership and initiative
• High level of communication (in order to transfer regulatory knowledge to non-regulatory audience)
• Being oriented on results and solutions
• Entrepreneurial thinking
• Living of our core values: achievement, entrepreneurship, ownership, partnership and responsibility
The skills for success
What we offer
Equality
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