Skip to content

Roche

Regulatory Specialist Diagnostics - Fixed term (6 months)

Roche is hiring a Regulatory Specialist Diagnostics - Fixed term (6 months) in Budapest, Hungary. Level rates it ; you can apply on Roche.

Level's read on this job

  • Level rates this role Little AI ●○○○: aI is not part of the work.
  • The posting mentions regulatory compliance, document management and regulatory affairs among its tools and skills.
  • Level classes it as a mid-level role.
  • Roche has 1,200+ other open roles on Level.
  • Posted within the past week.

AI in this role

Compile and maintain regulatory documentation and product registrations for diagnostics products on a fixed-term basis.

regulatory-compliancedocument-managementregulatory-affairsrims

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.

How we rate this

Regulatory Specialist Diagnostics - Fixed term (6 months) at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Regulatory ComplianceDocument ManagementRegulatory AffairsRims

Questions you could be asked

  1. Tell me about a project where regulatory compliance was part of your work. What did you do?
  2. Tell me about a project where document management was part of your work. What did you do?
  3. Tell me about a project where regulatory affairs was part of your work. What did you do?
  4. Tell me about a project where rims was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Regulatory Compliance, Document Management, Regulatory Affairs, and Rims. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

Get your CV reviewed before you apply

Send your CV and the role you want next. Your review arrives by email within 3 days.

Get new AI jobs by email

One email a week, each job rated for how much AI is in the work. No recruiter spam, unsubscribe in one click.

Free.

Similar roles

Other roles that involve little AI, at other companies.

What kind of AI work fits you?

Answer 12 practical questions in about three minutes. Get a simple profile, the work it points to, and live roles to explore next.

Find my next step

More jobs at Roche

Related searches

Same AI level

Jobs by city