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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: This role offers impactful work in regulatory affairs with opportunities for growth and influence.
- Qualifications: A Life Science degree and 3+ years of regulatory affairs experience are 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 help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the regulatory affairs field. Attend industry conferences or webinars to connect with others who work in similar roles, as they can provide valuable insights and potentially refer you to opportunities.
✨Tip Number 3
Prepare to discuss your experience with regulatory compliance and stakeholder management in detail. Be ready to share specific examples of how you've influenced stakeholders and driven service improvements in your previous roles.
✨Tip Number 4
Stay updated on the latest trends and changes in regulatory affairs, especially regarding GDP compliance and licensing requirements. This knowledge will not only enhance your expertise but also show your proactive approach to the field.
We think you need these skills to ace Regulatory Specialist
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Specialist position. Highlight key responsibilities and qualifications that resonate with your experience and skills.
Tailor Your CV: Customize your CV to reflect your relevant experience in regulatory affairs, particularly focusing on compliance, stakeholder interaction, and any specific licenses you have managed. Use keywords from the job description to align your application with the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory affairs and patient safety. Mention specific examples of how you've ensured compliance and improved processes in previous roles, and express your enthusiasm for working in a dynamic pharmaceutical environment.
Highlight Your Skills: In your application, emphasize your strong interpersonal and communication skills, as well as your problem-solving abilities. Provide concrete examples of how you've influenced stakeholders and led change management projects in the past.
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 regulations 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. Discuss how you implemented business improvements and influenced stakeholders to ensure successful outcomes.
