Roche Posted September 12, 2026

Regulatory Affairs Intern

Mississauga, Ontario, Canada FULL_TIME
Regulatory Affairs Intern/Fellow/Postdoc
Notify me about similar jobs

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 Regulatory Affairs Chapter is committed to ensuring patients have access to improved outcomes more quickly. Our strategic focus is on building, submitting, and obtaining approvals for clinical trial applications, new drug submissions, and new indications. Additionally, we collaborate with external partners to shape regulatory policies that eliminate barriers, enabling faster access to medications and therapies for patients.

The Opportunity

Supports the Regulatory Affairs team in the preparation of various regulatory submissions to Health Canada (ie, Clinical Trial Applications and Amendments, Investigational Testing Authorizations, New Drug Submissions, Medical Device Applications, Supplemental New Drug Submissions, Notifiable Changes, and Level III Changes), publishing activities, and responses to Health Canada queries.

Responsible for actively participating in cross-functional meetings for regulatory submissions, working closely with relevant local and global stakeholders (Product Development Regulatory, Pharma Technical Regulatory, Product Development Operations, GxP, etc.)

Accountable for keeping up-to-date with evolving Canadian Regulations to facilitate decision-making and ensure regulatory compliance

Contributes to the development and maintenance of Canadian Standard Operating Procedures (SOPs), process maps, and operating guides that are aligned to our Canadian regulatory requirements (Food and Drug Act and Regulations; Medical Device Regulations)

Keeps up to date on relevant internal electronic document management systems used for regulatory projects to be able to efficiently execute day-to-day activities (eg. Regulatory Information Management System etc), and supports cross-functional processes

Maintains departmental regulatory information-sharing framework (gDrives, gSites, OneArchive, etc.)

Participates in departmental objectives pertaining to process optimization

Who you are:

You hold a Bachelor’s Degree in Science

You are currently enrolled in a post-graduate program in a relevant field (ie, Humber College’s Regulatory Affairs program; Seneca College’s Pharmaceutical Regulatory Affairs & Quality Operations program)

Preferred:

You demonstrate strong interpersonal and communication skills, strong problem-solving skills, and strong project management and planning skills

General understanding of Health Canada regulations and guidelines

Microsoft Office and Google Suite skills are required

Basic understanding of automation and artificial intelligence (AI) concepts and applications (ie, OpenAI, Microsoft CoPilot, Notebook LM, Gemini)

Additional Information:

Duration (12 months), work term (Full time, 35 hours per week) and will begin in January 2027

Location: Based in Mississauga, Ontario.

Our team follows a hybrid work structure (minimum 3 days in the office).

The expected salary range for this position based on the primary location of Mississauga is 57 416,00 and 75 358,50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.

We use artificial intelligence to screen, assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

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
Intern/Fellow/Postdoc
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Mississauga, Ontario, Canada
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 21 comparable Intern/Fellow/Postdoc Regulatory Affairs roles across 10 biopharma companies.

21Comparable roles tracked
16Currently active
10Companies hiring similar roles
11Countries represented

Salary context

2 of 21 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate, Quality Records · Pfizer $64,600/yr – $107,600/yr
Peer group range $86,100 – $129,100 (median $107,600)

Where these roles are based

Top locations among the 21 comparable roles

United States8
Germany2
India2
Côte d'Ivoire1
Bulgaria1
Turkey1

+ 5 more countries

Seniority mix

21 of 21 peers have a known seniority level

Intern/Fellow/Postdoc11
Associate10

Therapeutic area mix

0 of 21 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.

50%similar
AstraZeneca Mississauga, Ontario, Canada Associate
Same function Adjacent seniority Same country
45%similar
Roche Singapore, Central Singapore, Singapore Intern/Fellow/Postdoc
Same function Same seniority
45%similar
Boehringer Ingelheim Istanbul, Turkey Intern/Fellow/Postdoc
Same function Same seniority
45%similar
STADA Arzneimittel Bad Vilbel, Germany Intern/Fellow/Postdoc
Same function Same seniority
45%similar
Boehringer Ingelheim Amman, Jordan Intern/Fellow/Postdoc
Same function Same seniority
45%similar
Boehringer Ingelheim Ridgefield, Connecticut, United States Intern/Fellow/Postdoc
Same function Same seniority

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.

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.

50%
Regulatory Affairs Associate Intern
AstraZeneca · Mississauga, Ontario, Canada · Associate
Function Therapeutic area Adjacent seniority Country
45%
Werkstudent Regulatory Affairs Germany (w/m/d) (Bad Vilbel, HE, DE, 61118)
STADA Arzneimittel · Bad Vilbel, Germany · Intern/Fellow/Postdoc
Function Therapeutic area Seniority Country
45%
Postdoctoral Regulatory Affairs Fellow - Product Strategy (Ridgefield, CT, United States, Connecticut)
Boehringer Ingelheim · Ridgefield, Connecticut, United States · Intern/Fellow/Postdoc
Function Therapeutic area Seniority Country
45%
Postdoctoral Regulatory Affairs Fellow - Product Labeling Content (Ridgefield, CT, United States, Connecticut)
Boehringer Ingelheim · Ridgefield, Connecticut, United States · Intern/Fellow/Postdoc
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.