Graduate - Regulatory Affairs

Caraway Therapeutics, Inc.

Greater London

Hybrid

GBP 32,000 - 36,000

Full time

7 days ago

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Benefits offered by this job

Hybrid work arrangement

Job summary

Caraway Therapeutics, Inc. in London offers a 24-month Regulatory Affairs Graduate Programme with rotations in International Regulatory Affairs CMC and UK Regulatory Affairs. The role provides exposure to regulatory strategy, submissions, compliance, and health authority engagement.

Based at Moorgate, London, in a hybrid setup and part of an international biopharma network. The programme targets graduates in science with strong communication, teamwork, and organisational skills, with flexibility

Qualifications

Currently studying towards, or recently completed a BSc in a scientific field.
Excellent communication and teamwork abilities.
Demonstrates integrity, accountability, and diversity values.
Shows initiative, proactivity, and digital curiosity.
Strong organisational skills and attention to detail.

Responsibilities

Complete 12 months in International Regulatory Affairs CMC.
Complete 12 months in UK Regulatory Affairs.
Support regulatory strategies and submission reviews for the EMEA/UK region.
Collaborate across teams to meet regulatory objectives and engage health authorities.

Skills

Communication

Teamwork

Integrity

Initiative

Organisational skills

Coordinate

Education

BSc in a scientific field

Job description

Job Description

24-Month Regulatory Affairs Graduate Programme featuring rotations in International Regulatory Affairs CMC and UK Regulatory Affairs, with exposure to regulatory strategy, submissions, compliance, and health authority engagement.

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 medicinal products, practices and solutions to the EMEA region, including the UK.

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.

Responsibilities:

12 months in International Regulatory Affairs CMC

In Regulatory CMC (Chemistry, Manufacturing and Controls) our experts maintain the scientific and technical aspects of products that ensure patients receive medicines that are manufactured and tested to a high quality and within compliance of the requirements of the world’s Health Authorities.

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 on‑time regulatory submissions.As part of the EMEA team you will be one of the regional experts for CMC in EU, Eastern Europe, Middle East and Africa.

Learn, assess, and apply regulatory policies, internal processes, and systems.
Support the development of regulatory strategies and the review of submission packages for the EMEA region.
Contribute to new marketing authorisation submissions and product lifecycle management activities.
Collaborate with colleagues across the region and globally to deliver regulatory objectives.
Participate in health authority interactions and support regulatory engagement activities.
Contribute to operational excellence and regulatory science initiatives while developing digital skills through the use of innovative tools and technologies.

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.

Support the development of regulatory strategies and regulatory submissions for new marketing authorisation applications and product launches.
Contribute to the lifecycle management of marketing authorisations, ensuring ongoing regulatory compliance.
Participate in MHRA interactions and support regulatory engagement activities.
Support the development and maintenance of patient information leaflets, packaging components, and artwork, in line with regulatory requirements and company procedures.
Develop and apply knowledge of UK and European regulatory legislation, guidelines, and processes.
Contribute to departmental projects, meetings, and cross‑functional initiatives across the Regulatory Affairs team.

Requirements:

Currently studying towards, or have obtained within the last two years, a BSc degree (or equivalent qualification) in a scientific discipline, such as Chemistry, Biological Sciences, Engineering, Pharmacy, Microbiology, Virology, Molecular Biology, Biochemistry, or a related field.
Strong communication and teamwork skills, with the ability to work effectively both independently and collaboratively.
Demonstrates integrity, accountability, and a commitment to diversity, inclusion, and organisational values.
Shows initiative, proactivity, and academic and digital curiosity, with a desire to learn and develop through feedback.
Strong organisational skills and attention to detail.

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 (Until August 2029).

Start Date:

September 2027

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 .

For more Information visit our Future Talent page!

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Required Skills: