About the Job
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.
We’re 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.
1. Execute downstream processing, sterile filtration of drug substance
Set up, maintain a variety of automated and manually operated equipment and perform production activities in downstream processes: clarification by centrifugation and TFF, purification by zonal centrifugation, splitting by continuous flow centrifugation, inactivation, diafiltration and sterile filtration of drug substance.
Perform troubleshooting and assessment of processes and technical problems.
Clean-in-place (CIP), cleaning-out-of-place (COP) of downstream equipment and vessels.
Provide training to personnel.
Execute and verify IQ/OQ/PQ validation and cleaning verification protocols. Ensure all equipment, instruments and systems are properly assembled, installed, tested and maintained.
Participate in preventive maintenance of production equipment and instruments.
2. Perform sampling and analytical tests - utility sampling, environmental monitoring and area-specific testing
Sample processed materials and perform in-process testing according to procedures.
Deliver samples to other departments on site as required.
Perform area-specific testing, utility sampling and environmental monitoring for production.
3. Maintenance of Clean rooms, Equipment, Inspection readiness
Perform routine cleaning and disinfection activities in classified environments.
Maintain and organize cleanroom in good cGMP state and ensure area is always inspection ready.
Submit equipment/material orders and maintain inventory of spare parts, purchased materials for downstream processing.
Maintain safe and clean work environment by following site procedures and cGMP regulations.
Participate in facility preparation and inspection readiness, safety and process audits.
4. Administration of data for drug substance operations
Document, review and maintain production and monitoring activities for drug substance manufacturing.
Draft, review and revise cGMP documents (SOPs/SWs, batch records, protocols, change controls, reports and other manufacturing supporting documents).
Analyze, enter & verify data on paper based or electronic documents.
Follow all SWls/SOPs and comply to site policies and procedures.
5. Participate in continuous process and equipment improvement, Health, Safety & Environment. Quality, and Inspection readiness initiatives
Perform and participate in continuous improvement and development projects. Support Deviations, CCR, CAPA in Quality system as needed and assist until completion as per committed due dates.
Participate in deviation investigations and root cause analysis.
Follow HSE SOPs, identify and minimize risks, promote safety culture.
Comply with HSE guidelines on the disposal of waste.
No employee has a proprietary right to an activity or group of activities.
Activities may be changed or reassigned to meet the needs of the operations.
Minimum Qualifications:
Education:
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.
Skills and Knowledge:
1. Functional, Technical or scientific
Purification Process.
Production Equipment.
Aseptic Technique.
Current Good Manufacturing Practices (cGMPs).
Knowledge and experience in Chemistry, Microbiology, Biochemistry.
Mathematics, Computer, Mechanical Aptitude, Technical Writing, Quality and Improvement, Safety.
2. Supervisory, Managerial and Personal
This is subject to change at any time and it should not be construed as limiting the right of the company to make such a change to meet the requirements of the operation.
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
Applications received after the official close date will be reviewed on an individual basis.
This position is for a current vacant role that is now open for applications.
Pay rate - 48.02 per hour
"Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company’s Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal, Data Subject Rights Webform. The Data Subject Rights Webform can also be used to request access or correction of your personal information and file a complaint.
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.
Thank you in advance for your interest.
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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Toute compensation sera déterminée en fonction de l'expérience démontrée. Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise. Des informations supplémentaires sur les avantages sociaux peuvent être trouvées ici.
