Roche Posted September 12, 2026

Regulatory Innovation & Sustainment Leader

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

As a Regulatory Innovation & Sustainment Leader  in the Pharmaceutical Development Regulatory (PDR) Innovation & Sustainment chapter, you will drive the digital transformation of regulatory workflows, specifically focusing on AI and data strategy. You will bridge the gap between business needs and technical execution, fostering a culture of innovation while ensuring operational excellence and compliance.

In PDR we develop and maintain our licenses - we influence Health Authorities in their thought process to develop regulations.

The Opportunity:

Strategic Leadership: Shape strategy and lead high-impact, complex, cross-functional project teams to deliver tangible business outcomes.

Domain Expertise: Serve as a recognized subject matter expert in Digital, AI, and Data, leveraging a broad cross-discipline skill set to drive innovation.

Team Empowerment: Cultivate a collaborative team culture where members are empowered to influence stakeholders and drive results.

Mentorship & Thought Leadership: Act as a go-to thought leader within PDR, coaching and upskilling junior colleagues to build internal capability.

Stakeholder Management: Influence cross-functional teams, including Health Authorities, government entities, politicians for key topics related to regulatory science and solution & sustainment. . Has established networks and utilizes networks with stakeholders external to Roche.

Change Management: Champion a culture of continuous improvement, experimentation, and VACC (Visionary, Architect, Coach, Catalyst) leadership principles.

Capability Building: Mentor colleagues, build talent, and manage complex, high-impact projects that unlock enterprise-wide benefits.

Who You Are:

Deep knowledge of process redesign for AI, data management practices with overarching business strategy to drive innovation.

Proven relevant work experience which includes supporting cross-functional teams in a scientific environment .

Proven ability to apply system thinking and an enterprise-wide mindset to lead change within a matrixed organisation.

Maintain a strong commitment to medical compliance, integrity, and the Roche Group Code of Conduct.

Expert-level ownership of complex, high-impact deliverables. Operates with distributed authority and accountability. Makes pragmatic, fit-for-purpose decisions, defaults to working transparently, and actively seeks advice to iterate and experiment.

Employs a continuous learning mindset and actively acts on feedback. Fosters community by prioritizing personal growth, teamwork, and self autonomy

Measurable reach and strategic results across the organization. Drives outcome-oriented results through strategic agility. Build, share, and leverage interconnected networks to exchange knowledge and advance key insights.

Demonstrated ability to influence and negotiate with global stakeholders and external entities by communicating transparently, listening actively and building mutual trust. Collaborates through iterative feedback while recognizing and elevating peer contributions.

Technical depth, practical expertise, and leadership maturity.

 

 

Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Welwyn. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.

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
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40%similar
Regeneron UK Limited Uxbridge1, United Kingdom Executive/VP
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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.