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About the Role

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster. Sanofi's global vaccines business unit partners with the public health, medical and scientific communities to improve access to life-protecting vaccines and increase vaccination coverage, while striving to develop new and improved vaccines to enhance health and well-being. At Sanofi, we chase the miracles of science to improve people’s lives. We believe our cutting-edge science and manufacturing, fueled by data and digital technologies, have the potential to transform the practice of medicine, turning the impossible into possible for millions of people.

Responsibilities

Administer Influenza manufacturing activities, including scheduling and coordinating daily/weekly work of technical staff.
Review records, SOPs, logbooks, BPRs, and monitoring charts for GMP compliance and accuracy.
Ensure equipment is maintained in good GMP condition through preventive maintenance, validation, and calibration.
Order and maintain adequate stock of chemicals, supplies, and spare parts.
Train technical staff on GMP and SOP requirements and ensure compliance.
Facilitate daily meetings and report findings to management.
Initiate and file deviations and lead investigations.
Coordinate with internal and external departments to ensure timely completion of production activities.
Supervise material handling in B200 Shipping, Receiving, and storage areas.
Administer data for Influenza manufacturing, including SAP activities and transactions.
Perform capacity planning and scheduling of materials and personnel.
Create work orders for ETS/Maintenance.
Maintain master recipes and production inventory.
Create and maintain process orders, with authorization to change orders.
Oversee and support environmental monitoring systems.
Ensure accurate and timely data input for investigations, LIMS, deviation filing, and change request forms.
Perform and review activities in PCS.
Perform and delegate production calculations, measurements, and release checks.
Ensure cleaning meets SOP, record, and GMP standards.
Observe and report process deficiencies, and perform visual inspection of equipment.
Perform and delegate utility sampling and environmental monitoring.
Train technical staff on problem-solving and troubleshooting.
Ensure the area is inspection-ready and guide inspectors.
Perform activities based on equipment access levels.
Oversee Health, Safety, and GMP environment maintenance.
Train technical staff on HSE requirements and ensure compliance.
Ensure operators use proper PPE.
Participate in HSE activities and support initiatives.
Ensure operations are performed ergonomically and escalate potential hazards.
Ensure routine HSE checks and inspections are completed.
Ensure cleaning chemicals and equipment are stored and used according to HSE requirements.
Maintain production and office areas in a tidy, GMP manner following 5S guidelines.
Clean and disinfect areas as required by SOP.
Coordinate and schedule technical staff work for facility, equipment, and process improvement projects.
Assist in the implementation of facility, equipment, and process improvement projects.
Write or modify specifications, protocols, and reports related to facility and equipment.
Perform activities for IQ, OQ, and PQ for new equipment.
Initiate and manage CCR and CAPA in the Quality system.
Collaborate with other departments for root cause analysis and corrective action implementation.

Requirements

Minimum 3 years College's degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science Degrees) plus a minimum of 36 months of previous relevant work experience.
Minimum 4 years Bachelor's Degree (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, other Life Science Degrees) plus a minimum of 36 months of previous relevant work experience.
Workday application form must be complete with a resume attached at the time of submission.

Skills

Microbiology
Protein purification
Basic mechanical skills
Aseptic Techniques
Chemistry
Mathematics
GMP
GLP
Computer skills
SAP
JMP
Visio
PCS
MES
e- BPR
e-logbook

Location

Toronto, ON

Work Type

Fixed Term Contract
Night Shift

Experience Level

36 months of previous relevant work experience

Education Level

3 years College's degree
4 years Bachelor's Degree

Salary/Compensations

$54.52 per hour

Benefits

High-quality healthcare
Prevention and wellness program

About the Company

Sanofi is an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth.
Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world.
Together, we chase the miracles of science to improve people’s lives.
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family.

Equal Opportunity

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.
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.