Technologue en contrôle de la production

Technologist

Fixed Term Contract - 8 months

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.

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.

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. 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 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).

• 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. 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. Material handling, movement an organization and storage. 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.
• 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. Follow HSE SOP's, identify and minimize risks, promote safety culture. Ensure chemicals are stored as per HSE requirement and has MSDS available.
• 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. 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.

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. OR 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.

Functional, Technical or scientific Purification Process for viral proteins Production Equipment. Aseptic Technique. Current Good Manufacturing Practices (cGMPs). Mathematics, Computer, Mechanical Aptitude, Technical Writing, Quality and Improvement, Safety.

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. 49.34 per hour

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

Artificial Intelligence 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. TheData Subject Rights Webformcan 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. Accommodations for persons with disabilities required during the recruitment process are available upon request.

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.Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.

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