Roche Posted September 12, 2026

LTO Regulatory Partner

Welwyn, Hertfordshire, United Kingdom FULL_TIME
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Roche is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

About Roche UK

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.

The Opportunity

Imagine working for an organization that puts people at the heart of everything they do, where your contributions directly impact patient outcomes. At Roche, our number one priority is our patients, and we believe that every person plays a key role in achieving this mission.

As a Regulatory Partner at Roche UK, you will be a vital part of our UK Regulatory Chapter. You will leverage your regulatory and scientific expertise to shape and drive strategic initiatives. This is your opportunity to make a difference and be part of a company dedicated to improving lives.

UK Regulatory Group Responsibilities

The Regulatory group collaborates with the wider business to translate the constantly evolving requirements of the UK regulatory environment into Roche policies, procedures, solutions, and strategies that ensure compliance and maximize the value for patients.

Our activities encompass:

Clinical Trial Applications

National Licensing Applications

Early Access to Medicines Applications

National components of medicines authorization via the European Centralized procedure

The team serves as Roche's primary contact with the MHRA, requiring effective cross-functional collaboration at both local and global levels, as well as the capability to negotiate and influence externally. Regulatory Partners need to be adaptable and entrepreneurial to identify opportunities, while maintaining a focused approach on ensuring compliance and playing a key role in retaining Roche UK's License to Operate.

Who You Are

You are a passionate regulatory expert with a clear vision for improving patient outcomes. With broad and comprehensive expertise within the UK regulatory environment, you will lead foundational work and partner with the business to solve complex regulatory issues impacting the chapter and/or wider business. You will contribute to the development of squad/chapter-based strategic plans and goals, and actively participate in the learning and development of other chapter members. You will have the ability to understand scientific and technical information relating to an assigned portfolio of Roche products.

You also bring :

A Scientific University degree

Extensive experience in UK Regulatory Affairs

Proven experience managing UK submissions post-Brexit

Experience providing strategic and technical advice

In-depth knowledge and experience of UK and EU regulatory requirements and procedures

A proven track record of developing, implementing, and communicating regulatory strategies

Excellent documentation skills to ensure high-quality and timely submissions

Experience as a Subject Matter Expert (SME) in defined subject areas or therapeutic areas

Experience in mentoring peers, as well as managing stakeholder relationships

 

 

 

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Welwyn, Hertfordshire, United Kingdom
Employment type
FULL_TIME

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 438 comparable Regulatory Affairs roles across 98 biopharma companies.

438Comparable roles tracked
404Currently active
98Companies hiring similar roles
52Countries represented

Salary context

119 of 438 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Associate, Quality Records · Pfizer $64,600/yr – $107,600/yr
Peer group range $86,100 – $380,750 (median $205,000)

Where these roles are based

Top locations among the 438 comparable roles

United States179
India35
Japan25
Ireland23
United Kingdom22
Poland18

+ 46 more countries

Seniority mix

348 of 438 peers have a known seniority level

Manager138
Director77
Associate Director45
Senior38
Executive/VP14
Senior Director13
Intern/Fellow/Postdoc12
Associate10
Principal1

Therapeutic area mix

36 of 438 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology18
Rare Disease5
Immunology4
Neuroscience3
Vaccines & Infectious Disease2
Cardiovascular / CVRM2
Dermatology & Aesthetics2

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
AbbVie Maidenhead, ENGLAND Manager
Same function Same country
40%similar
AbbVie Maidenhead, ENGLAND Manager
Same function Same country
40%similar
AbbVie Maidenhead, England Director
Same function Same country
40%similar
Regeneron UK Limited Associate Director
Same function Same country
40%similar
Regeneron UK Limited Uxbridge1, United Kingdom Executive/VP
Same function Same country
40%similar
Amgen Limited Uxbridge, United Kingdom Manager
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Senior Regulatory Affairs Manager, Europe
AbbVie · Maidenhead, ENGLAND · Manager
Function Therapeutic area Seniority Country
40%
Associate Director, Global Patient Advocacy
Regeneron UK Limited · Location not listed · Associate Director
Function Therapeutic area Seniority Country
40%
Executive Director, Regulatory Affairs Strategy - Cell Therapy
AstraZeneca · Cambridge, United Kingdom · Executive/VP
Function Therapeutic area Seniority Country
40%
Director, Regulatory Affairs, Labelling
Ipsen Biopharm Ltd · London (UK), United Kingdom · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.