Roche Posted November 10, 2026

Regulatory Specialist Diagnostics - Fixed term (6 months)

Budapest, Pest, Hungary 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

The Opportunity:

As a Regulatory Specialist you will be responsible to compile documents and deliverables to support planned product registration timelines. You will maintain product registration throughout a product’s lifecycle by applying successful regulatory change control. You will maintain clear agreement with other functions, stakeholders, and external partners (such as health authorities, companies, and notified bodies) to promote success of the registration activities and strategies. Collaborates with other functions in the organization to obtain regulatory approvals for products with defined markets.

Please note that this is a fixed-term position for a duration of 6 months.

Compile essential regulatory documentation for multiple products within a dedicated project, ensuring the continued compliance of our on-market portfolio and maintaining our license to operate. This position involves collaboration with diverse stakeholders and managing the end-to-end lifecycle of a specific regulatory document; from creation to final release into our document management system.

Provides support to currently marketed products, e.g., labeling, product and manufacturing changes and documentation for compliance and for changes requiring regulatory agency approval, as pertains to regulatory requirements. This includes annual reporting and laser reporting in relevant countries.

Interfaces with internal stakeholders to collect data to prepare, maintain regulatory documentation. This includes internal documentation decisions and review of analytical data report review and authoring of relevant analytical documentation.

Maintain documentation of the Regulatory Information Management System and create and maintain product information on the Regulatory Information Management System

Create reports on Regulatory Information Management System

Responsible for maintenance of product technical files and for ongoing activities related to compliance with Global Regulatory directives and regulations

Support for documentation management system workflows and support for any appropriate submission activity

Who you are:

Bachelor's/Master's degrees or equivalent experience

0-3 years experience, in Regulatory, R&D, Quality, Operations and/or Clinical. Fresh graduates are also welcome.

Equivalent experience may be satisfied by having completed training as a technician, a laboratory technician, or an equivalent qualification

Fluent in English, additional languages ( German or French or Latvian or Polish or Slovene or Turkish)  is a plus

Proven ability to work autonomously

In exchange we provide you with:

Development opportunities: Roche is rich in learning resources. We provide constant development opportunities, free language courses & training, the possibility of international assignments, internal position changes and the chance to shape your own career.

Excellent benefits: Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party.

Flexibility: We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average).

A global inclusive community, where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion.

Please read the Data Privacy Notice for further information about how we handle your personal data related to the recruitment process: https://go.roche.com/budapest-data-privacy-notice-candidate

 

 

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
Budapest, Pest, Hungary
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 544 comparable Regulatory Affairs roles across 109 biopharma companies.

544Comparable roles tracked
500Currently active
109Companies hiring similar roles
49Countries represented

Salary context

127 of 544 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
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $123,250 – $380,750 (median $201,250)

Where these roles are based

Top locations among the 544 comparable roles

United States216
India44
United Kingdom42
Japan38
Ireland21
China20

+ 43 more countries

Seniority mix

429 of 544 peers have a known seniority level

Manager172
Director78
Senior57
Associate Director52
Senior Director25
Intern/Fellow/Postdoc17
Associate11
Principal10
Executive/VP7

Therapeutic area mix

53 of 544 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology17
Oncology15
Rare Disease6
Vaccines & Infectious Disease4
Ophthalmology4
Neuroscience3
Cardiovascular / CVRM2
Dermatology & Aesthetics1
Respiratory1

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.

25%similar
AbbVie Director
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Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

Open in 2 locations

North Chicago, United StatesFlorham Park, United States
25%similar
Novartis 本社, Japan
Same function

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25%similar
Gilead Sciences K.K. Tokyo, Japan Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Mylan Inc. Washington, United States Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Generics [U.K.] Ltd. Lisbon, Portugal
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Mylan Pharmaceuticals Inc. Washington, United States
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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.

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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.

25%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
25%
Senior Regulatory Affairs Manager
Gilead Sciences K.K. · Tokyo, Japan · Manager
Function Therapeutic area Seniority Country
25%
Head of US Regulatory Affairs Advertising and Promotion, Global Regulatory Affairs
Mylan Pharmaceuticals Inc. · Washington, United States · Seniority not listed
Function Therapeutic area Seniority Country
25%
Director, Regulatory Strategist
Mylan Inc. · Washington, United States · 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.