Level

Roche

Regulatory Affairs Intern

Roche is hiring a Regulatory Affairs Intern in Abidjan, Côte d’Ivoire. Level rates it ; you can apply on Roche.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • Tools and skills the posting cites include regulatory affairs, compliance and pharmaceuticals.
  • Level classifies it as an internship.
  • Level lists 1,200+ other open roles at Roche.
  • The role was posted within the past week.

AI in this role

Roche is seeking a Regulatory Affairs Intern to coordinate regulatory submissions and ensure compliance with pharmaceutical standards.

regulatory-affairscompliancepharmaceuticalsregulatory-submissionsdocument-coordination

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 role:

We are looking for 1 intern who wants to be part of our Medical Affairs & License to Operate chapter in the regulatory affairs department.  The Regulatory Affairs intern performs the coordination and preparation of document packages for regulatory submissions to ensure alignment and compliance with local and regional registration requirements as well as with company policies, SOPs, internal audits, and inspections. Compiles all materials required in submissions, license renewal, and annual registrations.

Your main responsibilities: 

  • Analyze and communicate internal and external regulatory intelligence 

  • Provide regulatory input into cross-functional Affiliate business meeting 

  • Filing: Adapt global product dossiers to local requirements, prepare and manage regulatory registration filings across product life cycles, monitor and communicate all regulatory filing status 

  • Perform affiliate regulatory activities on relevant Roche systems

  • Ensure regulatory inspection-readiness for the Affiliate

  • Ensure regulatory compliance for products released to market according to marketing authorizations 

  • Review promotional and non-promotional material

Who are we looking for? 

You, as an ideal candidate, will have the following experience, education, and knowledge:

  • Recent graduate with no more than 2 years of experience 

  • University Degree in Pharmacy / Medicine or other relevant Pharmaceutical or Biological Disciplines. 

  • Pharm D preferred

You, as an ideal candidate, will have the following skills:

  • Fluence in French

  • Basic knowledge of English (written & spoken) with clear commitment on improving your language skills 

  • Eager to learn, self-managed & directed, bold, and being able to prioritize

  • The ability to work with cross-functional teams is a must

  • Ability to understand and leverage digital means and tools

  • Ability to deeply listen, question & understand, and communicate smoothly

 

 

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 Affairs Intern 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 AffairsCompliancePharmaceuticalsRegulatory SubmissionsDocument Coordination

Questions you could be asked

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

Adapt your resume

  • List these exact terms on your resume: Regulatory Affairs, Compliance, Pharmaceuticals, Regulatory Submissions, and Document Coordination. 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.

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