Technologist – Downstream cP – Toronto, ON

Sanofi US

Reference No. R2661845

Position Title:
Technologist – Downstream cP – Toronto, ON

Fixed-Term – Contract End Date: April 8, 2024

cP Team 4

Sanofi Pasteur Limited / Toronto, Ontario

Sanofi Pasteur: The world’s leading vaccine company

Sanofi Pasteur, the vaccines division of Sanofi, is the largest company in the world devoted entirely to human vaccines. Our driving goal is to protect people from infectious diseases by creating safe and effective vaccines. Our company distributes more than 1 billion doses of vaccine each year, making it possible to vaccinate more than 500 million people across the globe. Sanofi Pasteur offers the broadest range of vaccines in the world, providing protection against 20 bacterial and viral diseases.

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

Major Activities of the Job

Administration of Downstream production activities:

  • Assist in review BPR, SOP, logbooks, and monitoring charts for completion and insurance of accuracy of all documents as per GMP guidelines.

  • Train technical staff comply to cGMP, HSE, and SOP requirements

  • Participate in daily meetings and report findings to management

  • Participate in deviation investigations.

  • Coordinate activities within CP department (Adsorptions, Upstream and MWS).

Health, Safety, Environment:

  • Wear appropriate PPE when performing tasks.

  • Drive culture of HSE in department.

  • Escalate any potential hazards, help develop proposed solutions.

  • Participate in HSE checks and inspection.

  • Follow safety procedures.

Purification and sterile filtration of CP antigens:

  • Operation of Centrifuges for precipitation purification of CP antigens.

  • Operation of column chromatography for isolation of CP antigens.

  • Operation of Ultrafiltration units used for processing CP antigens.

  • Sterile filtration of CP antigens using aseptic technique and tube welder.

  • Perform and prepare for analytical tests such as lowry, Bradford and SDS-PAGE.

  • Assist in problem solving and trouble shooting.

  • Ensure area is inspection ready. Knowledgeable to guide inspectors.

Administration of Data Information for cP Production:

  • Complete SAP transactions in a timely, accurate manner.

  • Perform Pharm Net Web activities.

  • Enter data accurately and in a timely manner such as Shop Floor Data, LIMs, Mater, Change Request Forms.

Process improvement and development:

  • Assist implementation of facility, equipment, and process improvement projects.

  • Assist in execution and writing of documents (specifications, protocols and reports) related to facility, equipment, and process improvement of production process.

  • Modification of SOPs and BPRs for new processes in accordance with change control policies.

  • Perform IQ, OQ, and PQ for new equipment.

  • Attend meetings with other support functions representing production as needed.

Preparation of Trending reports and SPC data analysis:

  • Assist with implementation of corrective actions in production.

  • Assist with CCR, CAPA as needed until completion as per committed due dates.


  • Participate in keeping the production area in a tidy, GMP manner, following 58 guideline (sort, straighten, shine, standardize, sustain).

  • Disinfect area as required in SOP.

  • Assist in ensuring loading dock and hallways are clean and unobstructed by materials or equipment, garbage is discarded daily to designated area outside production.

  • Assist to ensure office area is kept in a tidy clean manner.

  • Supply air lock with gowning materials.

  • Animate visual management tools.

Minimum Qualifications

  • Minimum four (4) years Bachelor’s Degree (Biochemistry, Microbiology, Bioengineering), plus a minimum four (4) years of previous relevant work experience.

  • Preferred two (2) year Master’s Degree (Biochemistry, Microbiology and Bioengineering), plus a minimum of three (3) years of 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, trouble-shooting 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.

Hours Of Work

Inclusive from

  • Saturday – Sunday: 6:00 a.m. – 2:00 p.m.

  • Monday – Wednesday: 1:30 p.m. – 9:30 p.m.

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.

Only those candidates selected for interviews will be contacted.

Sanofi, Empowering Life


At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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