At a Glance
- Tasks: Oversee compliance and lead submissions for product approvals in Northern Europe.
- Company: Reckitt, a global leader in consumer health with a dynamic work culture.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a fast-paced environment with excellent career advancement opportunities.
- Why this job: Make a real impact on product compliance and regulatory strategies in a global setting.
- Qualifications: Experience in regulatory affairs and strong collaboration skills.
The predicted salary is between 63000 - 77000 £ per year.
Reckitt is seeking a Regulatory professional for Northern Europe (UK & Ireland) to oversee compliance, lead CMC submissions, and ensure timely regulatory strategies across NEU.
You will collaborate with cross-functional teams and interact with regulatory authorities to support product approvals and changes.
You will drive regulatory plans, manage submissions, and uphold high standards of quality and timeliness in a dynamic, global consumer health environment.
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Regulatory Affairs Associate – Northern Europe in Slough employer: Reckitt Benckiser LLC
Reckitt Benckiser LLC is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of Nottingham. Employees benefit from comprehensive growth opportunities, competitive compensation, and the chance to make a significant impact on global manufacturing standards. Join us to be part of a forward-thinking team dedicated to enhancing efficiency and driving technological advancements in a globally recognised supply chain.
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We think this is how you could land Regulatory Affairs Associate – Northern Europe in Slough
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We think you need these skills to ace Regulatory Affairs Associate – Northern Europe in Slough
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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 Benckiser LLC that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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