Sanofi Vaccines Canada Ltd. Posted October 21, 2026

Technologist

Toronto, Canada Full time
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Sanofi Vaccines Canada Ltd. 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

Reference no:  R2875211

Position title:  Technologist

Duration: Fixed Term Contract  - 11 months.

Location:  Toronto, ON

About the Job

Join a global network that powers how Sanofi delivers, seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.​

Sanofi Vaccines

Sanofi's global vaccines business unit partners with the public health, medical and scientific communities to improve access to life-protecting vaccines and increase vaccination coverage, while striving to develop new and improved vaccines to enhance health and well-being.

At Sanofi, we chase the miracles of science to improve people’s lives.  We believe our cutting-edge science and manufacturing, fueled by data and digital technologies, have the potential to transform the practice of medicine, turning the impossible into possible for millions of people.

About Sanofi 

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities:  

1. Efficient and Effective Execution of Testing Following Departmental SOPs/Approved Testing Protocols

Receive test samples and transfer to the appropriate testing area.

Perform testing, read andreportresults.

Submit microbial colonies recovered from testing for identification, when appropriate.

Prepare cultures and perform relevant microbial identity tests when appropriate.

Communicate and resolve issues with TGL/Manager and/or the appropriate department.

Assist with troubleshooting of invalid/unexpected results Assist with coordination of testing schedule, as required

Ensure that LIMS / SAP functions for all testing activities are completed in an accurate and timely manner. Communicate with Manager and QC planner to resolve outstanding items in SAP/LIMS and other related issues.

Compile data summary or trending reports with graphs /tables as needed

Ensure GMP/GLP and safety practices are followed.

2. Maintenance of Quality Systems

Ensure compliance is maintained in all daily activities by following SOPs, protocols and procedures as they apply. Ensure that a good documentation practice is observed in all documentation.

Review and verify test results performed by other analysts.

Identify and notify Manager of any laboratory non-conformances

File deviation reports as necessary and provide required support documentation to expedite closures of deviations

Participate in laboratory investigations and assist Lead investigator in preparation of investigation report.

Participate in root cause analysis to identify appropriate corrective actions for CAPAs and events.

Act as Change Control Initiator or Leader as needed

Create and reconcile controlled testing worksheets in the Electronic Document Management system.

3. General Maintenance of Work Area, Test Related Equipment and Supplies

Responsible for general maintenance of work area including cleaning of facility, equipment maintenance and disposal of hazardous waste.

Monitor and maintain inventory of test related materials and supplies. Liaison with purchasing, receiving and vendors.

Ensure the appropriate cleaning /equipment logs or other related records are completed and maintained as per the established procedures.

Report damages/ abnormalities to TGL/Manager and/or Security. File and follow-up on notifications for equipment, cleaning and maintenance services.

4. Training

Complete On-the-job training according to current Lesson plans, and document as required. Attend and participates in relevant training sessions continuously.

Review relevant SOPs/literatures continuously.

Participate in regularly scheduled GMP updates and safety training.

Attend departmental meetings and safety meetings.

Contribute to the establishment of training programs for the department and assist in training of new staff or existing personnel as required.

5. Participate in Specialized Projects/Continuous Improvement of Existing Testing

Write/ train on validation protocols and reports

Prepare data and documents using company's approved format

Assist Manager /TGL in planning and/or coordinating of project activities

Attend team meetings and performs the respective test as required.

Compile data summary with graphs /tables and prepare reports as needed

No employee has a proprietary right to an activity or group of activities. Activities may be changed or reassigned to meet the needs of the operations.

About You

​ Education:

Minimum four (4) years Bachelor's degree (Microbiology) plus a minimum of two (2) years of previous relevant work experience.

OR

Minimum four (4) years Bachelor's degree and two (2) years Master's degree (Microbiology), plus a minimum of eighteen (18) months of previous relevant work experience.

Skills and Knowledge:

1. Functional, Technical or Scientific skills/knowledge

Microbiological Methodology

Aseptic Technique

Microscopy

Well developed Computer Skills

2. Supervisory, Managerial and Personal skills/knowledge

Strong Communication skill - verbal and written

Judgement

Self-initiative /Focus

Accuracy/Attention to Detail

Demonstrated ability to work in team environment and cooperate transversally

Hours Of Work:

Inclusive from Monday to Friday 10:00 AM - 6:00 PM.

​

​This is subject to change at any time and it should not be construed as limiting the right of the company to make such a change to meet the requirements of the operation.

Pay rate - $49.34 per hour

Mandatory Application Requirement: Your Workday application form must be complete, and a copy of your resume MUST be attached in the Workday application form, at the time you submit your Workday application, otherwise your application will not be considered for this position

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness program

This position is for a new vacant role that is now open for applications.​

AI Usage

"Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company’s Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal,   Data Subject Rights Webform . The  Data Subject Rights Webform  can also be used to request access or correction of your personal information and file a complaint.

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants.  Accommodations for persons with disabilities required during the recruitment process are available upon request.

Thank you in advance for your interest.

#GD-SP ​

#LI-SP​

#LI-Onsite​

Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Toronto, Canada
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3753 comparable Manufacturing & CMC roles across 173 biopharma companies.

3753Comparable roles tracked
3372Currently active
173Companies hiring similar roles
64Countries represented

Salary context

921 of 3753 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
Lowest disclosed · Biologics Support Operator I (3rd Shift) · AbbVie $14/hr – $26/hr (≈ $29,099–$54,122/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $41,610 – $381,150 (median $125,550)

Where these roles are based

Top locations among the 3753 comparable roles

United States1739
Germany251
India166
France146
Ireland137
China123

+ 58 more countries

Seniority mix

1670 of 3753 peers have a known seniority level

Senior431
Manager381
Intern/Fellow/Postdoc259
Associate162
Principal138
Associate Director119
Director115
Senior Director57
Executive/VP8

Therapeutic area mix

24 of 3753 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

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
ID Biomedical Corporation of Quebec Quebec, Canada
Same function Same country
40%similar
ID Biomedical Corporation of Quebec Quebec, Canada
Same function Same country
40%similar
Sanofi Vaccines Canada Ltd. Toronto, Canada
Same function Same country
40%similar
Gilead Alberta ULC Edmonton, Canada
Same function Same country
40%similar
40%similar
AstraZeneca Hamilton, Ontario, Canada Associate Director
Same function Same country

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.

Or follow a whole field: get every new Manufacturing & CMC job in Canada, and choose locations and companies.

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%
Superviseurs de production
ID Biomedical Corporation of Quebec · Quebec, Canada · Seniority not listed
Function Therapeutic area Seniority Country
40%
Refrigeration Facilities Operator
Sanofi Vaccines Canada Ltd. · Toronto, Canada · Seniority not listed
Function Therapeutic area Seniority Country
40%
Associate Director, Supply Chain Planning
AstraZeneca · Hamilton, Ontario, Canada · Associate Director
Function Therapeutic area Seniority Country
40%
Site General Manager, TGO Canada
Teva Pharmaceuticals · Toronto, Ontario, Canada · Manager
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.