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Added 11 mins ago
SS
Mechanical Technologist
Surrey Schools (School District #36 Surrey)
Surrey, BC
- Full-time
A Mechanical Technologist provides technical support and supervises, directs and coordinates the work in one or more of the following technology areas: architectural, structural,…
Added 26 mins ago
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Added 1 hour ago
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Added 1 hour ago
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…expanding its Ontario operations and looking to add a Civil Engineering Technologist or Engineer-in-Training (EIT) to its growing…
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Architectural Quality Inspector
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Added 2 hours ago
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Bolton, ON
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Added 2 hours ago
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The Software validation Technologist plays a critical role by working within the Innovation and Sustainability Team, helping to bring physical testing results to component and system…
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Test Engineering Technologist
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…powerful risk prioritized product development process.The Test Engineering Technologist plays a critical role by working within the Innovation and Sustainability Team, helping to bring…
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Kraken Robotics is currently recruiting for a Manufacturing Engineering Technologist to join our team in Dartmouth, NS.
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Senior Internal Corrosion Advisor
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Municipal Engineering Technologist
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Added 3 hours ago
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Civil Engineering Technologist
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We are currently seeking a Civil Engineering Technologist to join our Linear Municipal Infrastructure team. Our team specializes in the critical networks that keep a community moving and…
Added 3 hours ago
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Added 3 hours ago
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Added 4 hours ago
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Analyst (Scheduler), Project Controls
EPCOR
AB · Edmonton, Alberta
- Full-time
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Sanofi

Technologist

Toronto, ON, Canada

Pay rate - $49.34 per hour · Full-time

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Job details

Pay: Pay rate - $49.34 per hour
Job type: Full-time
Apply by: Nov 10, 2026
Posting language: English
Posted: Nov 4, 2026

Original job description

Reference no: R2876183

Position title: Technologist

Duration: Fixed Term Contract - 8 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. Execution of Media, Buffer, Washing, and Sterilization & Inoculation preparation activities

Assist in review of Records, SOP, logbooks, and monitoring charts for completion and ensure accuracy of all documents as per GMP guidelines.
Train and ensure technical staff comply to GMP, HSE, and SOP requirements.
Participate in daily meetings and report findings to management.
Participate in deviation investigations and root cause analysis.
Coordinate with units within department (MWS, Upstream and Downstream)
Provide training to personnel.
Execute and verify IQ/OQ/PQ validation and cleaning verification protocols.
Perform other duties as assigned by department management throughout all stages of drug substance manufacturing related to (MWS, Upstream and Downstream processes).

2. Preparation of media, buffer, washing and sterilization, inoculum, analytical testing, area monitoring, maintenance, material handling, warehouse

Perform activities and documentation involved in MBWS and Upstream including, in buffer preparation, washing and sterilizing, inoculation preparation, infectivity testing, and material handling.
Perform production calculations, measurements, and release checks. Ensure each cleaning meets standards set in SOP, records, and in accordance with GMP.
Observe in detail and report any process deficiencies, perform visual inspection of equipment for impurity and damage before and after cleaning.
Perform utility sampling and environmental monitoring as required and ensure the completion as adhered to schedule.
Provide guidance to technical staff on problem solving and trouble shooting.
Ensure area is inspection ready. Knowledgeable to guide inspectors.
Material handling, movement an organization and storage. Reorder parts as per guidance from TGL's.

3. Administration of data for drug substance operations and preparation of trending reports for analysis

Document and review production and monitoring activities for drug substance manufacturing
Complete SAP transactions in a timely, accurate manner.
Draft, review and revise cGMP documents (SOPs/SWis, batch records, protocols, change controls, reports and other manufacturing supporting documents).
Ensure all data is completed timely and accurately in LIMS, Master, Change Request Forms, PCS and EM svstem.

4. Health, Safety and Environment and maintenance of GMP environment

Participate in keeping the production area and office areas in a tidy, GMP manner, following 5S guideline or equivalent and supply materials as required
Disinfect area as required in SOP.
Assist to ensure loading dock and hallways are clean and unobstructed by materials or equipment, garbage is discarded daily to designated area outside production.
Use proper PPE when performing tasks.
Follow HSE SOP's, identify and minimize risks, promote safety culture.
Ensure chemicals are stored as per HSE requirement and has MSDS available.

5. Process improvement and development

Assist implementation of facility, equipment, and process improvement projects.
Assist in writing specifications, protocols and reports related to facility, equipment, and process improvement of production process.
Modification of SOPs and BPR's for new processes in accordance with change control policies.
Perform activities involved in IQ, OQ, and PQ for new equipment.
Initiate Deviations, CCR, CAPA in Quality system as needed and assist until completion as per committed due dates.
Collaborate with other departments for root cause analysis and assist with implementation of corrective actions.

About You

Education:

Minimum (3) three years College diploma or equivalent (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science, or equivalent) plus a minimum of 18 months of previous relevant work experience.

Minimum (4) four years Bachelor's degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science, or equivalent) plus a minimum of (1) one year of previous relevant work experience.

Skills and Knowledge:

Functional, Technical or scientific

Purification Process for viral proteins
Production Equipment.
Aseptic Technique.
Current Good Manufacturing Practices (cGMPs).
Knowledge and experience in Chemistry, Microbiology, Biochemistry.
Mathematics, Computer, Mechanical Aptitude, Technical Writing, Quality and Improvement, Safety.

Hours Of Work:

Inclusive from Tuesday-Saturday or Sunday-Thursday or Friday to Tuesday from 02:00 PM to 10:00 PM (Subject to change).
Training schedule inclusive from Monday to Friday 08:00 AM - 04:00 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

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!

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More about this job

Responsibilities

The technologist will execute media, buffer, and sterilization preparation activities while ensuring compliance with GMP and HSE guidelines. They will also document production data, perform equipment validation, and assist in process improvement projects.

Requirements

Candidates must hold at least a three-year college diploma or a bachelor's degree in a relevant life science field. Additionally, they require 12 to 18 months of previous relevant work experience and proficiency in aseptic techniques and GMP standards.

Skills

Aseptic technique
GMP
Biochemistry
Microbiology
Purification process
Technical writing
Root cause analysis
Data documentation
Equipment validation
Environmental monitoring
SAP
LIMS
Quality control
HSE compliance
Material handling
Troubleshooting

Benefits

Health insurance
Prevention and wellness program
Supportive team environment
Career growth opportunities

Visa sponsorship

Not detected in the job text

Keywords

Sanofi
Manufacturing
Biopharma
Vaccines
GMP
SOP
HSE
Upstream
Downstream
IQ/OQ/PQ
SAP
LIMS
Aseptic technique
Biochemistry
Microbiology
Biotechnology
Chemical engineering
Pharmaceutical sciences
5S
CAPA
CCR
Deviations
Root cause analysis
Environmental monitoring
Material handling
Drug substance manufacturing
Validation
Quality assurance
Technical writing
Data management

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