Roche Posted August 15, 2026

Regulatory AI & Automation Specialist

Sabana Norte, San Jose, Costa Rica FULL_TIME
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Roche has closed or removed this posting -- see current similar openings below.

View the original listing (may no longer be live).

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 AI & Automation Specialist , you will be responsible for acting as the strategic bridge between regulatory science and technology, driving digital transformation within the PDR organization. In this role, you will design, develop, and implement intelligent automation and generative AI solutions, eliminating repetitive tasks and optimizing operational processes to bring efficiency and agility to a global community of over 500 regulatory professionals.

The Opportunity

Design, develop, and deploy scalable automation solutions (such as RPA, Python scripts, UiPath workflows, or No-Code/Low-Code tools) to optimize global regulatory processes.

Research, experiment with, and implement applications based on Artificial Intelligence (AI), machine learning, and natural language processing (NLP) tailored to regulatory document management.

Partner closely with business analysts, regulatory subject matter experts, and global leaders to map current operational processes and identify critical automation opportunities.

Provide ongoing technical support, preventive maintenance, and troubleshooting for automation and AI solutions already deployed in production.

Author and maintain rigorous technical documentation, including solution architecture, source code, user guides, and testing methodologies.

Design and deliver internal training programs to empower regulatory teams in the adoption and effective use of AI and automation technologies.

Present performance metrics, project updates, and strategic recommendations to business stakeholders and organizational leadership (with a scope of influence aligned to the experience level).

Who you are

University degree in Computer Science, Data Science, Software Engineering, Health Sciences with a strong technological focus, or a related field.

Proven experience in designing and developing process automation (RPA) solutions, workflows, and implementing AI tools (minimum 2–3 years for a Junior profile; 4+ years for a Senior profile).

Solid technical and programming skills in languages such as Python, SQL, and automation environments (UiPath, Power Automate, or Cloud platforms), along with familiarity with Agile methodologies (Scrum/Agile).

Understanding of pharmaceutical regulatory frameworks and industry registration procedures is highly valued.

Fluent and advanced English language skills (both written and spoken) to effectively interact, influence, and present findings to global teams across multiple time zones.

Excellent interpersonal skills, a system-thinking mindset, resilience, and a strong passion for innovation focused on radically simplifying business processes.

No relocation benefits are offered for this position.

 

 

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.

Roche is an Equal Opportunity Employer.

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Sabana Norte, San Jose, Costa Rica
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
405Currently 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
United Kingdom23
Ireland23
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

Currently open similar roles

This posting is closed, but here are live openings closest to it -- ranked by similarity, not by how well you'd qualify for them.

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Roche Sabana Norte, San Jose, Costa Rica
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25%similar
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25%similar
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25%similar
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25%similar
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25%similar
AbbVie Maidenhead, ENGLAND Manager
Same function

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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%
Regulatory Affairs Specialist
Roche · Sabana Norte, San Jose, Costa Rica · Seniority not listed
Function Therapeutic area Seniority Country
25%
Associate Director/Director, GRA, Regulatory Affairs Head – Canada
Lilly · Ontario, Ontario, Canada · Associate Director
Function Therapeutic area Seniority Country
25%
Senior Manager, Regulatory Affairs
AbbVie · Maidenhead, ENGLAND · Manager
Function Therapeutic area Seniority Country
25%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · 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.