Sanofi

Manufacturing & Supply

EquipmentSpecialist

$0–0k Toronto, Ontario, Canada FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Equipment Specialist at Sanofi. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. Oversee production activities and ensure smooth day-to-day operations. Set-up and troubleshoot production equipment to maintain adherence to production schedule”

What You'll Achieve.

Ensure smooth operation of influenza manufacturing processes; Ensure timely completion of production support activities; Maintain adherence to production schedule; Ensure completion of cleaning and sanitation post-troubleshooting activities, as required; Maintain all production equipment by complying with operations preventative maintenance and some calibration schedules; Ensure the completion as adhered to schedule; Ensure production area is kept in a tidy, GMP manner by implementing lean methodologies; Ensure production areas are inspection ready at all times; Ensure routine HSE checks and inspections are completed in timely manner; Ensure equipment is operated and maintenance activities are performed as per HSE guidelines; 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

Industry & Context.

Manufacturing & Supply
Problems you'll solve

Proven problem solving/judgment; Ability to troubleshoot quickly upon startup of production equipment to rectify or propose timely solution to keep production on schedule

Eligibility Requirements

Fixed Term Contract (24 months), Follow and adhere to equipment Lockout/ Tagout and De-energizing procedures when required

What They're Looking For.

Must Have

Minimum of eighteen (18) months of previous relevant 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

Nice to Have

Three (3) years College Diploma (Engineering, Science, Biotechnology or Equivalent) plus a minimum of two (2) years of previous relevant work experience

What You'll Do.

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

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

Perform Autonomous Maintenance on production equipment

Perform administrative activities for Manufacturing operations

Participate in continuous process and equipment improvement and maintain cGMP compliance

Oversee Health & Safety activities in GMP environment

How You'll Work.

Team & Collaboration

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; Communicate with TS Maintenance and create notifications in SAP for Maintenance work orders; Support planned maintenance activities & perform post-inspection test for proper equipment functionality; Support internal/external audits & inspections

Communication Scope

Communication

Full Job Description

**Reference no****:** R2857286 **Position title:** Equipment Specialist **Duration: **Fixed Term Contract (24 months) **Location:** Toronto, ON **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. **About Sanofi** 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. ** _Main Responsibilities:_ ** **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 equival

Free ATS check

Applying for this Equipment Specialist role?

Most applicants get filtered before a human reads their resume. See if yours makes the cut.

How to Apply on Workday

  • Workday has a multi-step form — save your progress after every section.
  • "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
  • Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
  • Job requisition numbers are useful when following up with HR by email.

ANONYMOUS · UNFILTERED

What do employees actually say about Sanofi?

Real rants from real employees. Read before you apply.

Read Company Rants →