Technologist

Sanofi•Toronto, ON

2d•Onsite

About The Position

Join Sanofi’s B200 Operations – MWS team as a Technologist. In this role, you will optimize media washing and sterilizing processes, ensuring the highest quality in biopharmaceutical production. Collaborate with cross-functional teams and drive innovation in a dynamic environment. 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.

Requirements

Minimum 3 years of college diploma in (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science.) with at least 1.5 years (18 months) of relevant work experience.
Knowledge of purification processes for viral proteins and production equipment, with proficiency in aseptic techniques and current Good Manufacturing Practices (cGMPs).
Strong background in chemistry, microbiology, biochemistry, and mathematics, supporting analytical and operational tasks.
Proficient in computer applications, with mechanical aptitude and technical writing capabilities for documentation.
Effective communication, teamwork, stress/time management, conflict resolution, and adaptability to thrive in dynamic environments.
Your Workday application form must be complete, and a copy of your resume MUST be attached in the Workday application form, at the time you submit your Workday application, otherwise your application will not be considered for this position

Nice To Haves

Preferred 4 years of Bachelor’s degree in (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science.) with 1 years of experience.

Responsibilities

Execute media washing, sterilization, and upstream activities while ensuring compliance with GMP guidelines through thorough review of records, SOPs, and monitoring charts.
Participate in deviation investigations and provide training to staff on GMP, HSE, and SOP requirements.
Coordinate with MWS, upstream, and downstream units, participate in daily meetings to report findings, and execute validation and cleaning verification protocols, supporting all stages of drug substance manufacturing in B200 operations.
Preparation of media, washing and sterilization, inoculum, analytical testing, area monitoring, maintenance, material handling, warehouse.
Document and review production and monitoring activities for influenza drug substance manufacturing, ensuring timely and accurate completion of SAP transactions and cGMP documents (SOPs, batch records, protocols, change controls).
Maintain data integrity in LIMS, Master, Change Request Forms, PCS, and EM systems.
Participate in keeping the production area and office areas in a tidy, GMP manner, following 5S guideline or equivalent and supply materials as required.
Process improvement, development, and preparation of trending reports for SPC analysis.