At a Glance
- Tasks: Support regulatory submission planning and manage operational projects across Europe, the Middle East, and Africa.
- Company: Join MSD, a diverse and inclusive employer at the heart of London.
- Benefits: Gain hands-on experience in a modern workspace with excellent amenities and support.
- Why this job: Make an impact in global regulatory affairs while learning from industry experts.
- Qualifications: Must be a UK university student seeking a 12-month internship.
- Other info: Flexible work arrangements and opportunities for process improvement await you.
The predicted salary is between 20000 - 30000 £ per year.
This role will be based in our modern state-of-the-art co-working facilities in Moorgate, London. This site, at the heart of London provides fantastic amenities, support services and collaborative workspaces with convenient transport links.
Brief Description of Position
You will work within our Global Regulatory Affairs and Clinical Safety (GRACS) organisation, in the Regulatory Affairs Operations International team, which is based in Europe. You will support the regulatory submission creation and the registration tracking of the company regulatory submission targets from a regulatory operational perspective across the Europe, Middle East, and Africa regions (EU & EEMEA). As a member of a cross-functional team and for the assigned products, you will support the team to manage all operational aspects for submission planning and execution of Original Marketing Application (OMA) and post-approval regulatory changes. This position requires a keen interest in the regulatory landscape, its registration procedures and a willingness to understand the technical requirements for dossiers.
Primary Activities include but are not limited to:
- Support the planning and managing of regulatory operation projects from authorisation through delivery to country regulatory affairs teams and/or Health Authorities.
- Supporting the regulatory submission plan for the assigned projects/products and maintaining the related project milestones.
- Participate in cross-functional forums and meetings.
- With manager support, drive the submission assembly and delivery process with the Global and/or Regional Submission Publishing team to ensure timely assembly, publishing and archival of assigned products/submissions as per the agreed timelines.
- Responsible for accessing and maintaining the regulatory systems and databases to fulfil daily functions.
- Assist in identifying opportunities to continually improve the efficiency of the submission processes and systems and participate in small-scale process improvement projects.
- Learn knowledge on the regional regulatory procedures on internal and external guidelines and standards.
Qualifications, Skills & Experience Requirements
You must be currently studying at a UK university and will be looking to complete a 12-month student internship as part of your undergraduate degree. Technical Requirements are flexible, but an affinity for and capability to learn Regulatory Information Management systems to execute operational tasks will be a significant asset.
How to Apply (Please Read): Please complete the online application form by answering questions within the application and upload your CV and Cover Letter in a combined document in the 'resume/CV' section.
Our standard Future Talent recruitment process is: An online application, a virtual conversation and then a final assessment.
Next Steps: In the event of your successful progression to the next stage, one of our future talent team will contact you within two - three weeks of the application closing date.
Start Date: June 2026
Equal Opportunity Employer: We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Student Placement - Associate Specialist, Regional Regulatory Operations, EU + EEMEA in Slough employer: MSD
Contact Detail:
MSD Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Student Placement - Associate Specialist, Regional Regulatory Operations, EU + EEMEA in Slough
✨Tip Number 1
Get to know the company! Research MSD and their values, especially their commitment to inclusivity. This will help you tailor your conversations during interviews and show that you're genuinely interested in being part of their team.
✨Tip Number 2
Network like a pro! Connect with current employees on LinkedIn or attend industry events. Building relationships can give you insider info about the role and even lead to referrals, which can be a game-changer in landing the job.
✨Tip Number 3
Prepare for virtual conversations! Practice common interview questions and have examples ready that showcase your skills and experiences relevant to regulatory affairs. Confidence is key, so rehearse until you feel comfortable.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about the opportunity. Make sure to follow up if you haven’t heard back after a couple of weeks!
We think you need these skills to ace Student Placement - Associate Specialist, Regional Regulatory Operations, EU + EEMEA in Slough
Some tips for your application 🫡
Tailor Your CV and Cover Letter: Make sure to customise your CV and cover letter for this specific role. Highlight your relevant skills and experiences that align with the job description, especially your interest in regulatory affairs and project management.
Show Your Enthusiasm: Let your passion for the regulatory landscape shine through! In your application, express why you're excited about this opportunity and how it fits into your career goals. We love seeing candidates who are genuinely interested in what we do.
Follow the Application Instructions: Pay close attention to the application process outlined in the job description. Make sure you complete the online application form and upload your CV and cover letter as a combined document. It’s all about making it easy for us to review your application!
Proofread Before You Submit: Before hitting that submit button, give your application a thorough read. Check for any typos or grammatical errors, as these can make a big difference. A polished application shows us you’re detail-oriented and professional!
How to prepare for a job interview at MSD
✨Know Your Regulatory Stuff
Make sure you brush up on the basics of regulatory affairs, especially in the EU and EEMEA regions. Familiarise yourself with the submission processes and key regulations that impact the role. This will show your genuine interest and understanding of the field.
✨Showcase Your Team Spirit
Since this role involves working in cross-functional teams, be prepared to discuss your experiences collaborating with others. Share specific examples where you contributed to a team project, highlighting your communication skills and ability to work towards common goals.
✨Ask Smart Questions
Prepare thoughtful questions about the role and the company culture. Inquire about the challenges the team faces in regulatory submissions or how they foster an inclusive environment. This demonstrates your enthusiasm and helps you gauge if the company is the right fit for you.
✨Practice Makes Perfect
Conduct mock interviews with friends or family to get comfortable with common interview questions. Focus on articulating your thoughts clearly and confidently. The more you practice, the more natural it will feel during the actual interview!