Job Details
Job Description
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.
We are a global biopharmaceutical leader committed to enhancing the lives of individuals through a diverse portfolio of prescription medicines, oncology treatments, life-saving vaccines, and animal health products. Our unwavering dedication to delivering innovative solutions is the driving force behind everything we do.
We offer an exciting 2-year graduate programme for graduates that are looking to work with us to deliver on our mission to save and improve lives. Our programme will give you the opportunity to collaborate alongside subject matter experts, bring your own ideas and share real responsibility whilst delivering on meaningful projects alongside a passionate, diverse and inclusive workforce.
Our Regulatory Affairs teams bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.
24 Month Graduate scheme encompassing two 12 month rotations in International Regulatory CMC (Chemistry, Manufacturing & Control), and Regulatory Affairs UK, both based at our Moorgate, London office.
You will spend…
12 months in International Regulatory International CMC
International Regulatory Affairs CMC is a key component of our company’s strategy to build regional Chemistry Manufacturing and Controls regulatory knowledge and effective local relationships with country offices to deliver appropriate regulatory strategies and deliver right first-time regulatory submissions. As part of the EMEA team you will be one of the regional experts for CMC in Europe, Middle East and Africa.
Duties & responsibilities
- Generate regulatory CMC strategies and Learn and apply regulatory policy
- Assess changes to dossiers in the EMEA region and review submission packages
- Liaise with colleagues across the region and globally
- Work alongside our team in health authority interactions and engagements
- Work alongside our team to deliver on operational excellence projects and best practises for regulatory science
And…
12 months in Regulatory Affairs UK
The Country Regulatory Affair team in the UK manages a broad portfolio of prescription medicines for the UK, largely across the vaccine, oncology and infectious disease therapeutic areas and this role is accountable for undertaking a variety of regulatory activities across a range of products for the UK market.
Duties & responsibilities
- Developing regulatory strategy and contributing to regulatory filing activities and documentation for new marketing authorisation (MA) applications and product launches.
- Life-cycle maintenance of all aspects of the MAs registered particulars.
- Work alongside our team in MHRA interactions and engagements.
- Generation and maintenance of prescribing information, patient information leaflets and packaging components, including artwork management, and ensure regulatory compliance with legislation and company approval systems.
- Developing and maintaining a knowledge of European and UK regulatory legislation and guidelines.
- Work alongside our team Contributing to departmental meetings, ad-hoc projects and issues.
Eligibility/Education
- Fields of study include (but are not limited to) Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry (or equivalent qualification)
Requirement: Skills, competencies and behaviours
- Operates with a high level of integrity, transparency and accountability
- Comprehends and aligns with our organization’s core values
- Aligns and fosters a culture of diversity and inclusivity
- Demonstrates initiative, proactivity and academic curiosity
- Encourages and boosts their colleagues through teamwork
- Demonstrates clear and effective communication
- Demonstrates a desire to learn and improve their performance through feedback
- Ability to work both independently and collaboratively in a team structure
Eligibility Criteria for Undergraduates:
We are looking for students based in the UK who complete their undergraduate degree between 2025 and 2027.
Important Note:
- We do not provide sponsorship for UK work visas during or after the graduate program.
- To be eligible for the 2-year program, you must have the right to work in the UK for its entire duration.
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.
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Job Details
About MSD
At MSD, we are inspired by a shared vision and mission to save and improve lives. For 130 years, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases in pursuit of our mission to save and improve lives.
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About MSD
At MSD, we are inspired by a shared vision and mission to save and improve lives. For 130 years, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases in pursuit of our mission to save and improve lives.
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Rating based on 24 Reviews
This score is based on honest feedback written by students who’ve worked at MSD.
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