Quality and Regulatory Trainee
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
This internship program offers students an opportunity to learn and develop within our Quality and Regulatory Subchapter. In this program, you'll gain insights into the diagnostics industry while upskilling and contributing to impactful projects for our patients.
We are looking for 1 intern who wants to be part of our Business Integrity team within the Quality and Regulatory department.
Your main responsibilities:
Support continuous updates of quality management system documentation by interacting with other areas of the company.
Support technical quality control activities for MD / IVD products.
Participate in a project to ensure vigilance contact availability for main hospital accounts.
Provide regulatory documentation translation support for tenders.
Participate in projects regarding Quality and Regulatory activities.
Who are we looking for?
As an ideal candidate, you will have the following experience, education, and knowledge:
Bachelors/Masters degree student in Health Sciences.
Languages: Spanish and English (advanced C1 level).
The applicant must be currently enrolled in a university to be eligible for a university internship contract.
As an ideal candidate, you will have the following skills:
Eager to learn, self-managed & directed, bold, and able to prioritize.
Attention to detail.
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.
What will you get out of this program?
Comprehensive professional experience that will allow you to acquire solid technical and practical knowledge in the diagnostics industry.
Soft skill training to manage projects and provide sustainable value to patients in a VUCA (volatility, uncertainty, complexity, and ambiguity) environment.
You will have a mentor who will support your development throughout the program.
Additional Responsibilities and Compliance
The Trainee (Intern) must comply with all applicable legislation, internal procedures, and regulations regarding Safety, Health, and Environment, especially those procedures related to waste segregation, application of preventive measures, and use of work equipment and personal protective equipment.
Furthermore, the Trainee (Intern) must be familiar with and act in full compliance with the Company's policies, including the Code of Conduct and applicable Ethical Codes.
Regarding Information Security, the Trainee (Intern) must:
Be aware of and comply with established quality and information security standards, and in any case, act according to instructions received.
Comply with and enforce applicable procedures.
Strive for the preservation of information security.
Provide suggestions and participate in the continuous improvement of developed activities.
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
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 644 comparable Quality roles across 85 biopharma companies.
Salary context
110 of 644 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.
Where these roles are based
Top locations among the 644 comparable roles
+ 39 more countries
Seniority mix
309 of 644 peers have a known seniority level
Therapeutic area mix
0 of 644 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
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.
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.
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.