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In the Media laboratory all duties performed are entered concurrently into Batch Production Records; each chemical is accurately selected, correctly labeled (using SAP system), weighed out in appropriate vessels and stored at the required conditions for the particular media being formulated. Performs daily or routine (as per schedule) calibration of pH meters, osmometers, weigh scales and balances; performs monitoring of magnehelic gauges, FMS (Facility Monitoring System) temperature and relative humidity and completion of other prescribed log books entries.

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R2796209 Technologist- VaccinesDuration: Fixed Term Contract End Date: April 30, 2026Location: Toronto, OntarioAbout the JobSanofi'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. Major Responsibilities:Efficiently, Operate and Complete Daily Tasks within the B90 Media Chemical. Raw Material Dispensing and Media Formulation Laboratory:<ul><li>Follow strict adherence to specific SOP's, cGMP's and specified process validation protocols.</li><li>Work with minimal supervision to maintain precise inventory of approximately 300 chemicals used in the preparation of over 250 buffers, acids, bases, agarsand tissue growth culture medium.</li><li>Manufacture large volumes in high demand to customers in Component. Pertussis (CP89 and CP90), PPD, Diphtheria, Tetanus, Final Product (Building90, 92), Adsorption Formulation (Building 90, 92), QC Bacteriology, M-Tech, Validation and Research and Development Departments.</li><li>Responsible for receiving chemical raw materials, scanning into SAP, labeling, thoroughly cleaning and wrapping with plastic to minimize dust and particulates, before placed in storage.</li><li>In the Media laboratory all duties performed are entered concurrently into Batch Production Records; each chemical is accurately selected, correctly labeled (using SAP system), weighed out in appropriate vessels and stored at the required conditions for the particular media being formulated.</li></ul>Formulation of Media and Diluents as per SOP's and cGMP:    <ul><li>Accurately formulate media:<ul><li>Complex Components Pertussis media for seed propagation, intermediate and production scale fermentation, critical buffers and dilution materials</li><li>Tetanus, Diphtheria, complex multi-stage media, removal of toxin inhibiting materials, filtration of media and preparation of diluents and intermediate buffers.</li><li>PPD, Final Formulation, Adsorption, for final dilution buffers, supply of adjuvant and support intermediate solutions.</li><li>M-Tech, QC Bacteriology, Validation, R&D in accordance with SOP's and cGMP's, under a highly controlled environment for testing solutions and final release test media</li></ul></li><li>Formulation of licensed materials is done independently, which includes the precise weighing of chemical components, thorough mixing with WFI, sterile filtration, the distribution to bulk containers and send samples to QC for testing.</li><li>Adjustment of pH by the addition of base or acid, dilution, conductivity reading, osmolality reading and filter integrity testing.</li><li>Requires extensive and detailed calculations and concurrent documentations as the job is being performed.</li><li>Verifier for co-worker when tasks are performed, materials are added, or in-process tests for pH, conductivity and osmolality are performed.</li></ul>Sterile Filtration of Final Product in Grade A/B Areas:<ul><li>Works independently within the clean room area executing the critical work via aseptic processes.</li><li>Thorough inspection of all equipment used within the clean room area and process related equipment.</li><li>Aseptic process to avoid contamination of materials or products, primarily responsible for the manufacturing of adjuvant used in the purified antigen process and in the final formulation process.</li><li>Preparation of clean room hoods and equipment set-up for the preparation of testing materials, dispensing of critical release-testing media plates, production related agar plates.</li><li>Performs final sterile filtration, dispensing and sampling of Aluminum.​, Phosphate, I 0% Triton, 5 % Tween 80 and other types of media.</li><li>Aseptically adjust pH by adding the base into the solution with precision and accuracy.</li><li>Extract QC samples from final bulk container for sterility and aluminum content.</li><li>During filtration, dispensing and sampling, extensive environmental monitoring must be performed including personal touch plates, settle plates, equipment touch plates, facility touch plates, air-borne particle counting, etc.</li><li>Perform semi-annual Aseptic Process Simulation Study for protocol review and creation of process orders for QO Sterility Testing via SAP.</li></ul>Calibration and Monitoring of Scientific Equipment and Systems:<ul><li>Performs daily or routine (as per schedule) calibration of pH meters, osmometers, weigh scales and balances; performs monitoring of magnehelic gauges, FMS (Facility Monitoring System) temperature and relative humidity and completion of other prescribed log books entries.</li><li>Maintenance of WFI system, sterile collection of WFI samples to be delivered for QC testing.</li><li>Performs appropriate environmental and personal monitoring according to strict schedules detailed in area SOP's and corporate policies.</li><li>Provide relevant information to Quality Operation Contamination Control in any investigation with regards to Environmental Incident Reports that occur in</li><li>Bacterial Media Production Area by providing all the requested data and documents to solve the issue.</li><li>Daily maintain all lab equipment to ensure proper function, certification and up to date.</li></ul>Accurate Record Keeping and Inventory Monitoring:<ul><li>Accurately and concurrently completes: batch production records, sample labels, and test requisitions, environmental monitoring data sheets.</li><li>Responsible for checking release and date status of all raw materials in SAP prior to use; makes all relevant SAP data entries and transactions related to inventory consumption and product formulation.</li><li>Order material via SAP and NEXT.</li></ul>Develops and Revises SOP's, BPR's Process Improvements/Efficiencies:   <ul><li>Suggest changes to SOP's and BPR's intended to streamline production methods.</li><li>Improve efficiencies, improve adherence to cGMPs or to assure better quality material.</li><li>Create new SOP's or BPR's when our customers require new media formulations.</li></ul>Sterile Filtration and Dispensing of Various Media Products in Class "C-Cl" Laboratories.<ul><li>Performs final sterile filtration dispensing of any media type made in class C-CI laboratories. The work must be performed aseptically.  During dispensing and sampling, extensive environmental monitoring must be performed including personal touch plate, settle plates, equipment touch plates, facility touch plate, air borne particle counting, etc. Integrity test of each liquid filter must be done pre-and post-use. Dispensing of agar plates, Roux bottles is also done in this area.</li></ul>About You<ul><li>Minimum three (3) years Diploma (Microbiology, Chemistry and Laboratory related courses), plus a minimum of three (3) year of previous relevant work experience.</li><li>Preferred three (3) years B.Sc (Microbiology, Chemistry, Biochemis), plus a minimum of one (1) year of previous relevant work experience.</li><li>Strong knowledge of Decision Making.</li></ul>Hours Of Work: <ul><li>Inclusive from Monday to Friday: 10:00 AM to 06:00 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 operationWhy 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- Vaccines

Asepsis

Bacteriology

Calibration

Chemistry

Cleanroom

Compensation Management

Corporate Policies

Current Good Manufacturing Practice (cGMP)

Datasheets

Diversity

Employee Retention

Environmental Monitoring

Equipment Maintenance/Repair

Housekeeping/Cleaning

International Business

Inventory Management

Inventory Transactions

Laboratory

Laboratory Equipment

Manufacturing

Materials Testing

Media Production

Medicine

Microbiology

Multimedia

New Media

Operational Control

Order Processing

Osmolarity

Problem Solving Skills

Process Improvement

Process Validation

Public Health

Quality Control

Research & Development (R&D)

Simulation

Specimen Collection

Standard Operating Procedures (SOP)

Systems Maintenance

Testing

Vaccination

Validation Plan

Water For Injection (WFI)

TMP PX

Operations Manager

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. Develop and execute production schedules from project through full-scale manufacturing, ensuring timely delivery of project milestones and deliverables.

R2807483 B200 Operations Manager (Media, Washing and Sterilizing)- Vaccines<div><div><div><div><div><div><div><div><div>Department: B200 Operations – Buffers, MWS & LogisticsDuration: Fixed Term Contract, 18 monthsLocation: Toronto, OntarioWe deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. The B200 MWS Manager is responsible for manufacturing operations in the Buffer Preparation, Washing & Sterilizing, and Raw Materials areas of Building 200. The manager is responsible for the daily acitivities of unionized staff in a cGMP facility in compliance with company policies. This includes responsibility for the scheduling and execution of all operations with adequate level of GMP documentation. This also includes active involvement in B200 project activities, from design to commercial operations.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. Main Responsibilities:<ul><li>Lead MWS processes and equipment operations through Development and PPQ through to Commercial Operation.</li><li>Develop and execute production schedules from project through full-scale manufacturing, ensuring timely delivery of project milestones and deliverables.</li><li>Ensure cGMP compliance and quality standards, develop continuous improvement initiatives, and support internal/external regulatory audits and inspections.</li><li>Author/Review/Approve technical documentation, work instructions, and SOPs.</li><li>Review and approve technical documentation (P&ID, IOQ, PPQ, design documents) and manage procurement of small equipment for engineering runs.</li><li>Implement lean management systems and lead continuous improvement initiatives to increase process efficiency, quality, and yield.</li><li>Provide troubleshooting and problem-solving guidance for daily manufacturing issues and implement preventative/corrective actions.</li><li>Ensure workplace safety compliance including HSE policies, HAZOP understanding, safety training, and incident reporting protocols</li></ul>  About You<ul><li>Bachelor's degree in microbiology, Biochemistry, Engineering, or Related Sciences required</li><li>Minimum 2-5 years pharmaceutical industry/manufacturing experience.</li><li>People management experience preferred</li><li>Experience with manufacturing automation (e.g., DeltaV) and electronic batch records preferred</li><li>Business/management training considered an asset</li></ul></div></div></div></div></div></div></div></div></div>Why Choose Us?<ul><li>Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.</li><li>Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs</li></ul>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.#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>

B200 Operations Manager (Media, Washing and Sterilizing)- Vaccines

Biochemistry

Biology

Biotech and Pharmaceutical

Continuous Improvement

Corporate Compliance

Corrective Action

DeltaV

Design Document

Detail Oriented

Documentation

Drug Manufacturing

External Audit

GMP (Good Manufacturing Practices)

HAZOP (Hazard and Operability Analysis)

Healthcare

Identify Issues

Infectious Diseases

Internal Audit

International Health

Lean Manufacturing

Logistics

Maintain Compliance

Manufacturing Automation

Manufacturing Management

Manufacturing Operations

Operations Management

Operations Processes

People Management

Power Amplifier

Procurement Management

Production Schedule

Project Schedule

Purchasing/Procurement

Quality Metrics

Regulations

Regulatory Compliance

Safety Compliance

Safety Training

Safety/Work Safety

Technical Writing

Time Management

Writing Skills

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