Technologist

Job type:; Toronto; On-site; CAD 90,000 - 120,000; Full time

Job summary

Sanofi in Canada is seeking a qualified Lab Scientist to join the Manufacturing & Supply team. The role focuses on coordinating routine immunochemical and instrumental assays and ensuring GMP/GDP-compliant testing and documentation.

The start date is January 2027 and the position supports in Toronto, Ontario. You will maintain test systems, support method transfers, and contribute to quality investigations while working in a collaborative, data-driven environment leveraging automated

Qualifications

• Bachelor’s degree in Chemistry/Biochemistry/Immunology/Biomedical Sciences or Molecular Biology with related lab experience.
• Experience with standard analytical assays and GMP/GDP principles preferred.
• Proficiency in MS Office, LIMS and data management.
• Strong technical writing and documentation skills.

Responsibilities

• Coordinate and perform routine immunochemical and instrumental assays (ELISA, LC-MS, HPLC, etc.).
• Maintain and calibrate lab equipment; ensure QA/QC procedures are followed.
• Assist in method transfer, validation, and deviations investigations.
• Prepare documentation and data for LIMS and QC release; manage samples and external labs.

Skills

Lab techniques

Immunochemical assays

Chemical assays

GMP/GDP knowledge

Computer skills

Technical writing

Education

Bachelor’s degree in Chemistry/Biochemistry/Immunology/Biomedical Sciences or Molecular Biology

Tools

MS Office

LIMS

SAP

FMS/BMS

Job description

The start date for this role is Jan 2027.

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’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. Coordinates and performs routine standard testing

• Responsible for coordinating and performing assigned routine immunochemical and instrumental assays within a team environment in accordance with existing SOPs (e.g. ELISAs, cell-based assays, SDS-PAGE/Densitometry, identity by Western Blot/Dot Blot/LC-MS/FTIR; HPLC, IC, GC, UV-VIS,TOC, Osmometry).
• Responsible for daily maintenance of test related equipment and system suitability, as required. Ensures that deaning procedures, calibration and or validation of equipment meets testing requirements, alerts others if issues arise. (ELISA plate washers/ readers, LC-MS and Chromatography systems, Densitometer, UV-VIS, FTIR, Biosafety cabinets, pipettes, balances, pH and Conductivity meters and weight sets.)
• Responsible for coordinating and performing routine in-house wet chemistry tests on in-process materials or final products (e.g. Nitrogen determination by micro-Kjeldahl, Aluminum by complexometric titration, identity by TLC).
• Perform wet chemistry/identity testing on Raw Materials according to in-house SOPs and Pharmacopoeias
• Assist with troubleshooting of invalid/unexpected results.
• Perform qualification of critical reagents according to SOPs, as required.
• Responsible for test reagent maintenance, inventory and supply and to ensure reagent supplies are replenished in a timely manner to avoid testing delays.

2. Documentation Testing and Support Documents

• Responsible for the timely and accurate completion and verification of test related documents to ensure on time delivery of test results. (e.g. data in LIMS, worksheets, log books, test requisitions, verification of calculations for accuracy, verification of entries and transcription of data, review of electronic data including audit trails, as applicable).
• Manage samples outsourced to approved contract labs including documentation preparation (Test Request and Shipping Form), review of test results (Certificates) from contract labs and transcription of results into LIMS or internal QC release documents, as required.

3. Maintenance of Quality Systems including adherence to GXPs and safety guidelines

• Ensures compliance is maintained in all daily activities by following SOPs (divisional, department & test), protocols and procedures as they apply. Reviews SOPs on an annual basis, documents training.
• Ensures that own training and qualification as per the qualification plan is current, with no overdue training.
• Responsible for identifying and notifying Manager of any laboratory non- conformances (deviations). Initiates LIRs and contributes to laboratory investigations and deviation reports as required, provides required documentation support to expedite closures of deviations. Participates in root cause analysis to identify appropriate corrective actions for CAPA and events.

4. General Maintenance of Work Area, Test Related Equipment, Chemical, Reagents and Lab Supplies

• Responsible for general maintenance of work area including cleaning of lab benches and all work surfaces, equipment maintenance and disposal of biohazardous waste and chemical waste.
• Responsible for performing and completing the assigned lab duties in a timely manner.
• Maintain general lab equipment (e.g. balances, fridges, freezers, water purification systems) and perform routine calibration checks, cleaning and preventative maintenance as required. Ensure the operation of equipment is satisfactory.
• Participates in projects for existing products and new products (e.g . collaborative studies with regulatory agencies and organizations on method comparison, assay/specification harmonization, new assay development, stability studies). Attend team meetings providing technical expertise on respective assays as required.
• Responsible for writing protocols and reports for test transfer and method validation as required.
• Execute studies under approved protocols for test transfer and new method validations, existing method revalidation.

6. Training / Skills Upgrade / Literature Review

• Complete On-the-job training according to current Lesson plans, and document as required.
• Participate in regularly scheduled GMP updates and safety training
• Complete the relevant and required tests and trainings on site procedures, USP, EP, ACS, etc. as required.
• Assist in training of new staff or existing personnel as required.
• Attend & participates (discussion & presentation) in relevant training sessions continuously.

About You

Education:

Minimum four (4) years Bachelor’s degree in (Chemistry, Biochemistry, Immunology, Biomedical Sciences or Molecular Biology), 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 in (Chemistry, Biochemistry, Immunology, Biomedical Sciences or Molecular Biology),plus a minimum of eighteen (18) months of previous relevant experience.

Skills and Knowledge:

1. Functional, Technical or Scientific

• Standard Analytical Lab Techniques (accurate transfer of weighed material, accurate volumetric measurement).
• Sound Knowledge and Practical Expertise in Immunochemical Assays.
• Sound Knowledge and Practical Expertise in Chemical/Biochemical Assays.
• Theoretical & Research related knowledge in Chemistry/Biochemistry, Immunology, Cell Biology.
• Sound knowledge of GMP requirements, including GDP.
• Computer knowledge – hardware, software, interfaces (e.g. MS Office, LIMS, SAP, FMS / BMS).
• Technical Writing Skills.

Inclusive from Monday to Friday 8:00 AM – 4:00 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.

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,can also be used torequest 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.

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Join Sanofi and step into a new era of science – where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.