Job Description

Job Description

R2805297 ​Equipment Specialist

Duration: Fixed Term , Oct 2027

Department: Upstream Influenza Vaccine Manufacturing

Location : Toronto, Ontario

Sanofi Vaccines

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. 

Major Activities of the Job:

Oversee production activities and ensure smooth day-to-day operations:

• Ensures smooth operation of influenza manufacturing processes.

• Reviews documentation for completion and accuracy as per cGMP guidelines (i.e. eLogbooks, eBRs, monitoring charts, etc.)

• Perform cleaning and ensure that clean rooms, equipment, and production instruments are maintained in good condition to maintain quality compliance requirements.

• Order and ensure adequate chemicals, materials, and spare parts are available for routine operations.

• Train and ensure operational staff comply to cGMP, HSE, and Quality requirements.

• Participate in daily +QDCI (or equivalent)

• Co-ordinate with units within department (MWS, downstream), other outside departments (Maintenance, Manufacturing Technology, QC, QO, etc.) and external vendors to ensure timely completion of production support activities.

Set-up and troubleshoot production equipment to maintain adherence to production schedule:

• Works to prepare assigned areas for the oncoming shifts and resolves production issues.

• Sets-up production lines prior to start-up of each batch.

• Ability to troubleshoot quickly upon startup of production equipment to rectify or propose timely solution to keep production on schedule.

• Perform minor repairs / part replacements on production machines and/or equipment when a malfunction has been detected.

• Observe in detail and report any process deficiencies, perform visual inspection of equipment for impurity and damage before and after cleaning.

• For unplanned work communicate with TS Maintenance and create notifications in SAP for Maintenance work orders (or any relevant system).

• Ensures the completion of cleaning and sanitation post-troubleshooting activities, as required.

Perform Autonomous Maintenance on production equipment:

• Performs SAP shop floor operational equipment preventive maintenance activities and makes repairs to production equipment or other area equipment as per procedures.

• Maintain all production equipment by complying with operations preventative maintenance and some calibration schedules.

• Order from maintained inventory of spare parts and consumables required for maintenance activities.

• Perform visual inspection of equipment for contamination and damage after maintenance activities.

• Support planned maintenance activities & perform post-inspection test for proper equipment functionality.

• Ensure maintenance activities are performed in an ergonomic way, escalate any potential hazards, and help develop proposed solutions.

• Support utility sampling and environmental monitoring as required and ensure the completion as adhered to schedule.

Perform administrative activities for Manufacturing operations:

• Complete quality documentation (eBRs, eLogbooks, Training Matrix, SAP or equivalent work orders etc.) accurately in a timely manner.

• Create Notifications for Maintenance SAP (or relevant system) work orders, for future planned work.

• Assist with deviation investigations and implementation of CAPAs.

• Request materials from MWS and ensure timely receipt for Upstream and Downstream operations.

• Ensure transactions are done in a timely, accurate manner.

• Ensure all data input is completed accurately and in timely manner.

• Trains and orients new team members as assigned in multiple areas.

Participate in continuous process and equipment improvement and maintain cGMP compliance:

• Assist with implementation of facility, equipment, and process improvement projects.

• Perform activities for qualification and validation as required.

• Assist with updating procedures and corresponding documentation (i.e., SOPs, SWIs, vendor documents, equipment documents etc.) for improving processes in accordance with change control policies.

• Ensure production area is kept in a tidy, GMP manner by implementing lean methodologies.

• Ensure production areas are inspection ready at all times.

• Support internal/external audits & inspections.

• Propose improvement ideas for equipment and processes based on technical knowledge.

Oversee Health & Safety activities in GMP environment:

• Ensure routine HSE checks and inspections are completed in timely manner.

• Ensure equipment is operated and maintenance activities are performed as per HSE guidelines.

• Support culture of HSE in department and support HSE initiatives.

• Ensure operators are equipped and use proper PPE when performing tasks.

• Ensure cleaning chemicals and equipment are stored and used as per HSE requirements and has SDS available.

• Follow and adhere to equipment Lockout/ Tagout and De-energizing procedures when required.

Minimum Qualifications:

• College Diploma in Engineering, Science, Biotechnology or equivalent.

• 18 months relevant prior work experience.

• Sound knowledge of Upstream, Downstream and MWS equipment and procedures.

• Sound knowledge of cGMP.

• Broad-based knowledge.

• Computer skills.

• Communication.

• Interpersonal & teamwork skills.

• Work under pressure.

• Proven problem solving/judgment.

Hours Of Work:

• Days/Afternoon

• Days - Sunday to Thursday 6:00 am - 2:00 pm (subject to change)

• Afternoon - Sunday to Thursday 2:00 pm - 10:00 pm (subject to change)

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

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

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.

Watch our ALL IN video and check out our Diversity, Equity and Inclusion actions at sanofi.com!

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.

Only those candidates selected for interviews will be contacted.

Follow Sanofi on Twitter: @SanofiCanada and on LinkedIn:

#GD-SP #LI-SP

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.

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.

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