At a Glance
- Tasks: Support compliance for medical devices and collaborate with cross-functional teams.
- Company: Join Reckitt, a leader in hygiene, health, and nutrition.
- Benefits: Inclusive culture, mental health support, competitive pay, and career growth opportunities.
- Other info: Dynamic work environment with opportunities to learn across various functions.
- Why this job: Make a real impact on global health and wellness through innovative regulatory practices.
- Qualifications: Degree in a scientific discipline or relevant experience; regulatory knowledge preferred.
The predicted salary is between 29700 - 36300 £ per year.
City: Kingston upon Hull
We are Reckitt, home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.
In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. 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:
The Regulatory Operations Specialist plays an essential role to achieve and maintain compliance and business continuity for our existing portfolio of medical devices across the whole product lifecycle, whilst also ensuring we are an effective, well-connected organisation.
Your responsibilities:
- Supporting post launch regulatory activities for all planned and unplanned compliance and maintenance activities for our medical device portfolio across all markets.
- Ensuring regulatory changes are implemented within our registration files on a global basis working on collaboration with regional RAS teams, RAS strategy teams and global cross functional partners (which include R&D, procurement, sustainability, supply, quality and any other department where regulatory support is required) with a right first time approach.
- Ensuring both planned and unplanned maintenance activities e.g. renewals are completed in a timely manner to ensure business continuity.
- Driving efficiencies and operational excellence within RAS, align on priorities and resourcing with the Regulatory Operations Team.
- Ensuring that you work according to internal and external standards, to ensure our products are compliant according to regulations and internal standards.
- Managing a complex and diverse set of regulatory requirements and landscape overview across multiple markets.
- Ensuring regulatory information on various systems and databases are kept up to date.
The experience we're looking for:
- Prior experience in Medical Devices or an equivalent regulatory classification is preferred.
- An ability to work on multiple projects at any given time and a capability to work with the line manager to prioritise and manage workload.
- You have the knowledge and understanding of regulatory requirements associated with Reckitt products. Medical Device experience is a benefit but not a requirement.
- You have high scientific credentials with a Bachelor of Science (BSc) / Master of Science (MS) degree in a relevant scientific discipline – such as Chemistry, Biological Sciences, Microbiology, Pharmacy, or significant applied industry experience.
- You have an ability to deliver to time, cost and quality standards in a fast paced, high-pressure environment.
- You have a strong collaborative mindset and able to form strong partnerships with cross functional teams.
- You have a basic understanding how to translate complex regulatory information into a compelling stakeholder friendly language.
- You strive for a high level of accuracy in authoring documentation, with a focus on ensuring the level of registered information is appropriate in the dossiers.
The skills for success:
- Task Execution Under Pressure
- Business Acumen
- Commercial Awareness
- Objective Setting
- Accountability
- Consumer Insight
- R&D
- Product Lifecycle Management
- Intellectual Property
- Business Partnership
- Collaboration and partnership building
- Adapt to changes in technological development plans
- Ability to challenge the status quo and propose improvement
- Innovation Processes
What we offer:
With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.
Equality:
We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.
Regulatory Operations Specialist - Medical Devices in Hull employer: Reckitt
Reckitt is an exceptional employer located in Kingston upon Hull, offering a dynamic work culture that prioritises inclusion and employee wellbeing. With access to the Research and Development Academy, employees can grow their skills while contributing to meaningful projects that aim to enhance global health and hygiene. The company also provides competitive benefits, including parental support, mental health resources, and opportunities for financial participation in Reckitt's success, making it a rewarding place to build a career.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Operations Specialist - Medical Devices in Hull
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Reckitt. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Reckitt.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Reckitt. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Reckitt is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Regulatory Operations Specialist - Medical Devices in Hull
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Reckitt!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Reckitt that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Reckitt!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Reckitt, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Reckitt
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Reckitt that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Reckitt’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.