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- Tasks: Join us as a Regulatory Affairs Associate, handling license maintenance and new marketing authorizations.
- Company: Work with one of the largest pharmaceutical companies tackling urgent medical needs globally.
- Benefits: Competitive pay, opportunity to work in a dynamic industry, and potential for career growth.
- Why this job: Make a real impact in healthcare while developing your skills in a supportive team environment.
- Qualifications: Bachelor’s degree in a scientific field and foundational knowledge of regulatory affairs required.
- Other info: Must be eligible to work in the UK; DBS check may be needed.
CK Group are recruiting for a Regulatory Affairs Associate, to join a company in the pharmaceutical industry, at their site based in Basingstoke, on a ontract basis for 12 months.
Salary:
PAYE £14.68 – £19.37 per hour.
Regulatory Affairs Role:
- License maintenance activities (e.g. Labelling changes, CMC changes, Renewals).
- New marketing authorisations, line extensions and new indications.
- Tracking regulatory procedures and filing/archiving correspondence in accordance with local regulations and quality system requirements.
- Provide operational excellence to successfully achieve affiliate regulatory objectives.
- Facilitate and cultivate relationships with relevant external regulatory personnel.
Your Background :
- Bachelor’s degree or equivalent in a relevant scientific subject.
- Foundational knowledge and understanding of regulatory environment.
- Good communication skills and the ability to prioritise different tasks.
- Demonstrated good computer/IT skills.
- Team working skills with special focus on results.
Company:
Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs.
Location:
This role is based at our clients site in Basingstoke.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference121 958 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Regulatory Affairs employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs
✨Tip Number 1
Familiarize yourself with the specific regulatory requirements in the pharmaceutical industry. Understanding local regulations and quality system requirements will give you an edge in discussions during the interview.
✨Tip Number 2
Network with professionals in the regulatory affairs field. Attend industry events or join relevant online forums to connect with people who can provide insights and potentially refer you to opportunities.
✨Tip Number 3
Highlight your communication skills and teamwork experience in conversations. Be prepared to discuss specific examples of how you've successfully collaborated on projects or communicated complex information.
✨Tip Number 4
Research the company’s recent activities and regulatory achievements. Being knowledgeable about their work will demonstrate your genuine interest and help you stand out during the interview process.
We think you need these skills to ace Regulatory Affairs
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Affairs Associate position. Understand the key responsibilities such as license maintenance activities and new marketing authorisations, as well as the skills required.
Tailor Your CV: Customize your CV to highlight relevant experience and skills that align with the job requirements. Emphasize your foundational knowledge of the regulatory environment and any previous experience in the pharmaceutical industry.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your communication skills and ability to prioritize tasks. Mention your enthusiasm for the role and how you can contribute to achieving the affiliate regulatory objectives.
Follow Application Instructions: When applying, ensure you quote the job reference 121 958 in all correspondence. Double-check that you meet the eligibility to work in the UK and include any necessary documentation.
How to prepare for a job interview at CK Group
✨Understand Regulatory Requirements
Make sure you have a solid grasp of the regulatory environment relevant to the pharmaceutical industry. Familiarize yourself with license maintenance activities, such as labeling changes and renewals, as these are crucial for the role.
✨Showcase Your Communication Skills
Since good communication is key in this position, prepare examples that demonstrate your ability to effectively communicate with both internal teams and external regulatory personnel. This will highlight your interpersonal skills.
✨Highlight Teamwork Experience
Be ready to discuss your experience working in teams, especially in achieving results. Share specific instances where your collaboration led to successful outcomes, as this aligns with the company's focus on operational excellence.
✨Demonstrate IT Proficiency
Given the importance of computer and IT skills in this role, be prepared to talk about your experience with relevant software and tools. Mention any specific systems you've used for tracking regulatory procedures or filing correspondence.
