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Document, review, and maintain production and monitoring activities for influenza drug substance manufacturing, including drafting, reviewing, and revising cGMP documents such as SOPs, SWIs, batch records, protocols, change controls, reports, and other supporting materials. Preferred 4 years Bachelor’s degree [Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences], plus a minimum of 12 months of previous relevant work experience.

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R2806394 Technologist - Flu Downstream- VaccinesDuration: Fixed-Term, 20 monthsDepartment: B200 Downstream Afternoon Shift 2Location: Toronto, OntarioAbout the JobSanofi is seeking a dedicated and skilled Technologist to join our B200 Downstream team for the afternoon shift. In this role, you will play a vital part in our biopharmaceutical production processes, ensuring the highest quality standards are met. We are looking for someone who is passionate about innovation and committed to making a difference in the healthcare industry. If you thrive in a collaborative environment and have a keen eye for detail, we invite you to apply and contribute to our mission of improving patient lives.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.Major Responsibilities:<ul><li>Perform downstream processing and sterile filtration of influenza drug substance. Set up and maintain automated and manual equipment, executing production activities such as clarification (centrifugation and TFF), purification (zonal centrifugation), splitting (continuous flow), diafiltration, and sterile filtration.</li><li>Perform sampling and analytical tests utility sampling, environmental monitoring and area-specific testing.</li><li>Maintain and organize cleanroom in good cGMP state and ensure area is always inspection ready.</li><li>Document, review, and maintain production and monitoring activities for influenza drug substance manufacturing, including drafting, reviewing, and revising cGMP documents such as SOPs, SWIs, batch records, protocols, change controls, reports, and other supporting materials.</li><li>Participate in continuous process and equipment improvement, Health, Safety & Environment, Quality, and Inspection readiness initiatives.</li></ul>About You:<ul><li>Minimum 3 years College Diploma [Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences], plus a minimum of 12 months of previous relevant work experience.</li><li>Preferred 4 years Bachelor’s degree [Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences], plus a minimum of 12 months of previous relevant work experience.</li><li>Knowledge of Purification Process for viral proteins.</li><li>Familiarity with Automated and manually operated process equipment.</li><li>Strong knowledge of Computerized systems.</li><li>Strong communication, Interpersonal skills.</li></ul>Hours Of Work:<ul><li>Inclusive from Monday - Friday: 2:00 PM- 10:00 PM. (will start off as 8:30 AM-4:30 PM).</li></ul>This is subject to change at any time, and it should not be construed as limiting the right of the company to make such change to meet the requirements of the operation.Why Choose Us?<ul><li>Bring the miracles of science to life alongside a supportive, future-focused team.</li></ul>Mandatory Application Requirement: 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 positionThis position is for a current vacant role that we are actively hiring for.​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.#GD-SP#LI-SP​ #LI-OnsiteAll compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can <a href="https://myflex-benefits.ca/en/home/" rel="nofollow">be found here.</a>Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise. Des informations supplémentaires sur les avantages sociaux peuvent <a href="https://myflex-benefits.ca/fr/home/" rel="nofollow">être trouvées ici.</a>

Sanofi

Technologist - Flu Downstream- Vaccines

Analysis Skills

Biochemistry

Bioengineering

Biotech and Pharmaceutical

Change Control

Chemical Engineering

Chemistry

Cleanroom

Communication Skills

Compensation Management

Current Good Manufacturing Practice (cGMP)

Detail Oriented

Diversity

Drug Manufacturing

Employee Retention

Environmental Monitoring

Healthcare

Infectious Diseases

International Health

Interpersonal Skills

Microbiology

Patient Care

Process Improvement

Production Control

Quality Metrics

Safety/Work Safety

Standard Operating Procedures (SOP)

Team Player

User Documentation

Vaccination

TMP PX

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