cP Upstream Technologist- Vaccines

Sanofi; Toronto; On-site; CAD 60,000 - 100,000; Full time

Job summary

Ein innovatives Unternehmen sucht einen engagierten Technologen für die cP Upstream-Abteilung im Bereich Bulk Manufacturing. In dieser spannenden Rolle werden Sie Teil eines dynamischen Teams, das an der Herstellung hochwertiger pharmazeutischer Produkte arbeitet, die die globale Gesundheit positiv beeinflussen. Sie werden an der Front der Innovation stehen und mit Fachleuten zusammenarbeiten, um Prozesse zu verbessern und sicherzustellen, dass alle Aktivitäten den GMP-Standards entsprechen. Wenn Sie eine Leidenschaft für die Wissenschaft haben und einen Unterschied machen möchten, ist dies die perfekte Gelegenheit für Sie.

Benefits

Unterstützendes Team

Karrieremöglichkeiten

Diversity und Inklusion

Qualifications

• Mindestens 4 Jahre Erfahrung in relevanten Bereichen.
• Starke Kenntnisse in Mikrobiologie und Fermentation.

Responsibilities

• Überprüfung von Dokumenten gemäß GMP-Richtlinien.
• Fermentation und Ernte von B. Pertussis für die Antigenproduktion.

Skills

Mikrobiologie

Fermentationstechniken

Aseptische Techniken

GMP-Kenntnisse

Problemlösung

Kommunikationsfähigkeiten

Education

Bachelor in Biochemie

Bachelor in Mikrobiologie

Bachelor in Bioengineering

Master in Biochemie

Master in Mikrobiologie

Master in Bioengineering

Tools

Datenmanagementsysteme

Job description

cP Upstream Technologist- Vaccines

Bewerben locations Toronto, ON

Time Type: Vollzeit

Posted On: Gestern

Time Left to Apply: Enddatum: 5. April 2025 (Noch 1 Tag Zeit für Bewerbung)

Job Requisition ID: R2787339

Duration: Fixed Term Contract-3 Years

Location: Toronto, Ontario

Are you ready to make an impactful contribution to the future of pharmaceutical manufacturing? We are seeking a dedicated Technologist to join our dynamic team in the cP Upstream department within Bulk Manufacturing. As a Technologist at Sanofi, you'll be at the forefront of innovation, collaborating with a passionate group of professionals to produce high-quality pharmaceutical products that positively impact global health.

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. 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.

Main Responsibilities:

1. Assist on review BPR, SOP, log books, and monitoring charts for completion and insurance of accuracy of all documents as per GMP guidelines.
2. Participate in keeping the production area tidy, in a GMP manner, following 5S guidelines (sort, straighten, shine, standardize, sustain).
3. Fermentation and harvest of B. Pertussis for cP antigens production.
4. Assist in writing specifications, protocols, and reports related to facility, equipment, and process improvement of production process.
5. Modification of SOPs and BPRs for new processes in accordance with change control policies.
6. Escalate any potential hazards. Help develop proposed solutions.
7. Participate in HSE checks and inspections.
8. Train technical staff to comply with cGMP, HSE, and SOP requirements.
9. Enter all data in a timely, accurate manner, such as Shop Floor Data, LIMs, Master, Change Request Forms.

About You:

1. Minimum four (4) years bachelor's degree (Biochemistry, Microbiology, Bioengineering), plus a minimum of four (4) years previous relevant work experience.
2. Preferred two (2) years master's degree (Biochemistry, Microbiology, Bioengineering), plus a minimum of three (3) years previous relevant work experience.
3. Strong knowledge of microbiology and fermentation processes.
4. Proficiency in aseptic techniques.
5. Familiarity with current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (cGLP).
6. Competent in computer skills, communication, stress and time management, initiative, problem-solving, and troubleshooting.

Hours Of Work:

Inclusive from Monday to Friday, 10:00 pm - 6:00 am. 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 new vacant role that is now open for applications.

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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