Regulatory Affairs & Safety Specialist Core_fixed-term
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.
For this role we are offering a limited contract, until August 2027.
Your responsibilities
- Responsible for all aspects of filing registrations and maintaining documentation compliance throughout the product life cycle
- Exercises the necessary authority to prepare and submit documents and product files for approval/authorization/notification to the appropriate agencies
- Collaborate with relevant local and global teams and the commercial teams in Croatia to establish and implement regulatory strategies within the agreed timeframes to execute the business plan for the commercialization of OTC medicine products
- Coordinate the resolution of regulatory issues affecting OTC products, advising the company on registration and regulatory issues
- Provide regulatory support and advice to internal and external clients in the region in a professional manner
- Collaborate closely with external partners, contractors and licensees to ensure that regulatory issues are properly managed and resolved
- Collaborate with the team while taking on independent responsibility for regulatory innovation and compliance activities
- Interpret and implement regulations and guidelines as needed to foster industry compliance
- Engage with trade associations, contributing to and utilising our resources to influence favourable legislation
- Understand the regulatory necessities of diverse projects, actively participate in them, and remain alert to project advancements and their benefits
- Manage updates and actions in your area, ensuring tasks are completed effectively and efficiently
The experience we're looking for
- University degree preferably in Pharmacy or Medicine
- At least 2-3 years of experience in Regulatory Affairs
- Fluent in Croatian and English
- Results-oriented, entrepreneurial and self-motivated
- Proficient in multitasking, executing tasks under pressure, and making objective decisions when faced with complex issues
- Acute business acumen accompanied by commercial awareness
- Demonstrated ability to cultivate insights from consumer interactions and translate them into strategic actions
- Skilled in collaborating with teams across various functions, fostering an environment of partnership building
- Agility to adapt to the ever-evolving technological landscape, complemented by a mindset that seeks to improve and advance current processes
The skills for success
What we offer
Equality
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