Technologist

Sanofi • Toronto, ON

6d • Onsite

About The Position

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 Department B100 Downstream is looking for a Technologist for a 3-years fixed-term contract. You'll drive innovation in downstream processing, enhance operational efficiency, and contribute to impactful projects. Join us to make a difference in biopharmaceuticals with a forward-thinking team. Apply now to be part of our journey! We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world. 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.

Requirements

• Minimum three (3) years College degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences).
• Minimum of two (2) years previous relevant work experience.
• Strong knowledge and familiarity with aseptic techniques, microbiology and cGMP, cGLP practices.
• Strong mechanical skills and problem-solving ability.
• Experience in setting-up, operating, troubleshooting and cleaning machinery as per SOPs.
• Demonstrated ability to work independently and make quick decisions in accordance with SOPs and training.
• Basic computer skills and the ability to enter data accurately and in a timely manner.

Nice To Haves

• Preferred four (4) years Bachelor’s degree (Biochemistry, Microbiology, Bioengineering), plus a minimum eighteen (18) months of previous relevant work experience.

Responsibilities

• Execute downstream processing, sterile filtration of drug substance
• Set up, maintain a variety of automated and manually operated equipment and perform production activities in downstream processes: clarification by centrifugation and TFF, purification by zonal centrifugation, splitting by continuous flow centrifugation, inactivation, diafiltration and sterile filtration of drug substance.
• Perform troubleshooting and assessment of processes and technical problems.
• Clean-in-place (CIP), cleaning-out-of-place (COP) of downstream equipment and vessels
• Provide training to personnel
• Execute and verify IQ/OQ/PQ validation and cleaning verification protocols.
• Ensure all equipment, instruments and systems are properly assembled, installed, tested and maintained.
• Participate in preventive maintenance of production equipment and instruments.
• Perform sampling and analytical tests- utility sampling, environmental monitoring and area-specific testing
• Sample processed materials and perform in-process testing according to procedures.
• Deliver samples to other departments on site as required.
• Perform area-specific testing, utility sampling and environmental monitoring for production.
• Maintenance of clean rooms, equipment, inspection readiness
• Perform routine cleaning and disinfection activities in classified environments.
• Maintain and organize cleanroom in good cGMP state and ensure area is always inspection ready.
• Submit equipment/material orders and maintain inventory of spare parts, purchased materials for downstream processing.
• Maintain safe and clean work environment by following site procedures and cGMP regulations.
• Participate in facility preparation and inspection readiness, safety and process audits.
• Administration of data for drug substance operations
• Document, review and maintain production and monitoring activities for drug substance manufacturing
• Draft, review and revise cGMP documents (SOPs/SWs, batch records, protocols, change controls, reports and other manufacturing supporting documents).
• Analyze, enter & verify data on paper based or electronic documents.
• Follow all SWls/SOPs and comply to site policies and procedures.
• Participate in continuous process and equipment improvement, Health, Safety & Environment, Quality and Inspection readiness initiatives.
• Perform and participate in continuous improvement and development projects.
• Support Deviations, CCR, CAPA in Quality system as needed and assist until completion as per committed due dates
• Participate in deviation investigations and root cause analysis.
• Follow HSE SOPs, identify and minimize risks, promote safety culture.
• Comply with HSE guidelines on the disposal of waste.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Education Level: Associate degree