Technologist - Flu Downstream- Vaccines

卡湯晩; Toronto; On-site; CAD 60,000 - 80,000; Full time

Job summary

A leading global healthcare company is seeking a Technologist for its B200 Downstream team. The role involves crucial responsibilities in biopharmaceutical production, emphasizing quality and innovation, with opportunities to work collaboratively in a dynamic environment. Candidates with relevant education and a passion for healthcare are encouraged to apply.

Benefits

Supportive and future-focused team atmosphere

Qualifications

• Minimum 3 years College Diploma with 12 months relevant experience.
• Knowledge of purification processes is crucial.
• Preferred Bachelor’s degree with similar experience.

Responsibilities

• Perform downstream processing and sterile filtration of influenza drug substances.
• Maintain cleanroom and ensure cGMP compliance.
• Document and review production activities.

Skills

Knowledge of Purification Process for viral proteins

Familiarity with Automated and manually operated process equipment

Strong knowledge of Computerized systems

Strong communication

Interpersonal skills

Education

Minimum 3 years College Diploma (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences)

Preferred 4 years Bachelor’s degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences)

Job description

R2806394 Technologist - Flu Downstream- Vaccines

Duration: Fixed-Term, 20 months

Department: B200 Downstream Afternoon Shift 2

Location: Toronto, Ontario

About the Job

Sanofi 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 500million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people andpromote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact onmillions of patients around the world.

Major Responsibilities:

• 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.

• Perform sampling and analytical tests utilitysampling, environmental monitoring and area-specific testing.

• Maintain and organize cleanroom in good cGMP state and ensure area is always inspection ready.

• 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.

• Participate in continuous process and equipment improvement, Health, Safety & Environment, Quality, and Inspection readiness initiatives.

About You:

• 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.

• 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.

• Knowledge of Purification Process for viral proteins.

• Familiarity with Automated and manually operated process equipment.

• Strong knowledge of Computerized systems.

• Strong communication, Interpersonal skills.

Hours Of Work:

• Inclusive from Monday - Friday: 2:00 PM- 10:00 PM. (will start off as 8:30 AM-4:30 PM).

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?

• Bring the miracles of science to life alongside a supportive, future-focused team.

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 position

This 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.

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Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

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.com!