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- Tasks: Ensure regulatory compliance and manage license submissions across UK, EU, and global markets.
- Company: Join a leading pharmaceutical organization dedicated to patient safety and compliance excellence.
- Benefits: Enjoy remote work flexibility with occasional travel and a dynamic team environment.
- Why this job: Make a real impact in regulatory affairs while working with top stakeholders and authorities.
- Qualifications: Life Science degree, 3+ years in regulatory affairs, strong communication, and problem-solving skills required.
- Other info: Interviews in November, with a start date planned for January.
The predicted salary is between 36000 - 60000 £ per year.
Are you ready to take the next step in your regulatory affairs career? We are partnering with a leading pharmaceutical organisation to find a skilled Regulatory Affairs Specialist who is passionate about ensuring compliance and safeguarding patient safety. This exciting role offers the opportunity to work across UK, EU, and global markets. Key Responsibilities Regulatory Compliance : Ensure adherence to regulatory requirements across UK, EU, and global regions, managing license submissions, variations, renewals, and inspections. Interaction with Regulatory Authorities: Acting as a key contact with regulatory bodies for inspections, audits or clarifications regarding services Stakeholder Support : Provide strategic guidance on regulatory requirements to senior management, liaise with regulatory authorities, and foster strong relationships with stakeholders. Licensing and Accreditation: Managing regulatory requirements for licenses, such as WDA and GDP compliance, ensuring the safe handling, storage and transport of medicines Qualifications and Skills A Life Science degree or equivalent professional qualification. Strong interpersonal and communication skills (written, oral, and presentational). Proven ability to influence stakeholders and drive service improvements. 3+ Years experience in within regulatory affairs Experience in regulatory strategy for importing and exporting in EU countries Strong problem-solving and analytical skills with a track record of delivering results in GDP environments. Experience leading change management projects and implementing business improvements. What We Offer This role is primarily remote, with occasional travel to London and very infrequent trips to the Netherlands. Join a forward-thinking team in a dynamic organisation committed to excellence in pharmaceutical compliance. Interviews will take place in November, with a planned start date in January. For any questions, feel free to reach out directly.
Regulatory Specialist employer: William Parker Group
Contact Detail:
William Parker Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Specialist
✨Tip Number 1
Familiarize yourself with the specific regulatory frameworks in the UK, EU, and global markets. Understanding the nuances of these regulations will not only boost your confidence but also demonstrate your commitment to compliance during discussions.
✨Tip Number 2
Network with professionals in the regulatory affairs field, especially those who have experience with pharmaceutical organizations. Engaging with industry peers can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss your previous experiences in managing license submissions and interactions with regulatory authorities. Highlighting specific examples where you successfully navigated complex regulatory challenges will set you apart.
✨Tip Number 4
Stay updated on current trends and changes in regulatory affairs, particularly those affecting the pharmaceutical industry. Being knowledgeable about recent developments will show your proactive approach and dedication to the field.
We think you need these skills to ace Regulatory Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Regulatory Specialist position. Tailor your application to highlight relevant experiences that align with these requirements.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 3+ years of experience in regulatory affairs. Provide specific examples of how you've ensured compliance and managed license submissions or inspections in previous roles.
Showcase Communication Skills: Since strong interpersonal and communication skills are crucial for this role, include examples in your application that demonstrate your ability to influence stakeholders and provide strategic guidance effectively.
Tailor Your Cover Letter: Craft a personalized cover letter that reflects your passion for regulatory affairs and patient safety. Mention your understanding of the regulatory landscape across UK, EU, and global markets, and express your enthusiasm for joining a forward-thinking team.
How to prepare for a job interview at William Parker Group
✨Know Your Regulations
Make sure you are well-versed in the regulatory requirements across the UK, EU, and global markets. Familiarize yourself with recent changes in legislation and be prepared to discuss how they impact compliance and patient safety.
✨Showcase Your Communication Skills
Since strong interpersonal and communication skills are crucial for this role, practice articulating your thoughts clearly. Be ready to provide examples of how you've effectively communicated with regulatory authorities or stakeholders in the past.
✨Demonstrate Problem-Solving Abilities
Prepare to discuss specific challenges you've faced in regulatory affairs and how you resolved them. Highlight your analytical skills and your ability to deliver results in GDP environments.
✨Highlight Your Experience with Change Management
Be ready to talk about any change management projects you've led or been a part of. Discuss how you implemented business improvements and the impact they had on regulatory compliance.
