Roche Posted July 9, 2026

Regulatory Innovation & Sustainment Professional - Quality and Compliance

Budapest, Pest, Hungary FULL_TIME
Regulatory Affairs

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

Join Roche Product Development Regulatory Affairs (PDR), a flexible, bold, and distinctive regulatory organization where we make strategic decisions quickly, innovate boldly, and deliver insights that shape our portfolio development. We are seeking a talented professional to help build, mature, and sustain our regulatory business capabilities while fostering a culture of continuous learning and meaningful impact for patients.

The Opportunity:

Support complex and higher exposure quality and compliance activities, providing guidance and risk assessment to PDR staff on GCP, GVP, MDR, and IVDR compliance issues, and serving as advisor and subject matter expert for Quality and Compliance-related processes

Lead deviation management and process management activities, updating and maintaining regulatory documents while sustaining Quality and Compliance operational activities required for maintaining Roche's license to operate and Quality Management System (QMS)

Oversee training management, scheduling training sessions and ensuring completion across PDR to support our commitment to regulatory compliance and continuous learning

Prepare and manage compliance reports, monitoring trends in the external compliance environment

Partner across the enterprise with stakeholders within and beyond PDR (including affiliates, PD quality organizations, and the broader Roche group) to unlock company-wide benefits and ensure regulatory compliance

Lead increasingly complex deliverables while collaborating cross-functionally with key stakeholders, generating insights, and mentoring peers to foster a culture of innovation and continuous improvement

Monitor and respond to trends in innovation and the external compliance environment, anticipating changes in the regulatory landscape and assessing future business needs

Contribute to initiatives that shape our technical, business, and healthcare environments, bringing new ideas into the business and leading them with entrepreneurial mindset

Who You Are:

5+ years of relevant regulatory affairs, quality, or compliance experience in the Pharma or Medical Device space, with a proven ability to independently deliver and lead increasingly complex projects and initiatives

Experience working with health authorities, understanding the global regulatory environment

Strategic and systems thinker with strong data management, content management, and knowledge management capabilities; experienced in change leadership and operating effectively in matrix environments

Cross-functional collaboration expert with demonstrated experience in building trusted partnerships across internal and external stakeholders, including health authorities

Compliance-focused professional with a deep understanding of the global regulatory environment, GCP, GVP, MDR, and IVDR requirements, and a commitment to maintaining license to operate and integrity

Continuous learner with a growth mindset, strong communication skills, and ability to seek and act on feedback

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 305 comparable Regulatory Affairs roles across 67 biopharma companies.

305Comparable roles tracked
275Currently active
67Companies hiring similar roles
37Countries represented

Salary context

85 of 305 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 · AVP, Therapeutic Area Head, Clinical Safety and Risk Management · Merck $378,100/yr – $595,100/yr
Peer group range $98,050 – $486,600 (median $205,000)

Where these roles are based

Top locations among the 305 comparable roles

United States124
Ireland25
India25
United Kingdom17
Poland16
Japan13

+ 31 more countries

Seniority mix

261 of 305 peers have a known seniority level

Manager112
Director61
Senior27
Associate Director26
Senior Director12
Executive/VP11
Associate8
Principal2
Intern/Fellow/Postdoc2

Therapeutic area mix

33 of 305 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology10
Dermatology & Aesthetics6
Neuroscience6
Immunology4
Cardiovascular / CVRM2
Rare Disease2
Respiratory2
Vaccines & Infectious Disease1

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
Roche Budapest, Pest, Hungary Associate
Same function Same country
25%similar
Lilly Indianapolis, Indiana, United States of America
Same function

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

25%similar
Lilly Shanghai, Shanghai, China Manager
Same function

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

25%similar
Lilly Bracknell, United Kingdom Principal
Same function

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

25%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function

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

25%similar
Lilly Ontario, Ontario, Canada Associate Director
Same function

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

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 Labelling Associate (Maternity cover)
Roche · Budapest, Pest, Hungary · Associate
Function Therapeutic area Seniority Country
25%
Sr. Principal Scientist, Advisor, Sr. Advisor of Global Regulatory Affairs Chemistry, Manufacturing & Controls and Devices-EMEA
Lilly · Bracknell, United Kingdom · Principal
Function Therapeutic area Seniority Country
25%
Senior Director-Global Regulatory Affairs - Global Regulatory Scientist
Lilly · Indianapolis, Indiana, United States of America · Senior Director
Function Therapeutic area Seniority Country
25%
Regulatory Affairs Associate Director
Lilly · Shanghai, Shanghai, China · Associate 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.