×
Register Here to Apply for Jobs or Post Jobs. X

CPMedia Technologist

Job in Toronto, Ontario, C6A, Canada
Listing for: Sanofi EU
Contract position
Listed on 2026-07-15
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Pharmaceutical Manufacturing
Job Description & How to Apply Below
Position: cP89 Media Technologist

Reference Number: R2862709

Position Title: cP89 Media Technologist

Duration: Fixed Term Contract - 24 months

Location: Toronto, ON

About the Job

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and  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 a 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

Administration of Media, Washing and Sterilization activities

  • Assist on review of Records, SOP, logbooks, and monitoring charts for completion and insurance of accuracy of all documents as per GMP guidelines.
  • Train and ensure technical staff comply to cGMP, HSE, and SOP requirements
  • Participate in daily meetings and report findings to management
  • Participate in deviation investigations
  • Coordinate with units within department (Upstream and Downstream)

Health, Safety, Environment

  • Wear proper PPE when performing tasks.
  • Drive culture of HSE in department.
  • Escalate any potential hazards in a timely manner. Help develop proposed solutions.
  • Participate in routine HSE checks and inspections.
  • Follow safety procedures.
  • Ensure chemicals are stored as per HSE requirement, and has MSDS available.

Preparation of media, washing and sterilization, analytical testing, area monitoring, maintenance

  • Perform accurate formulation calculation and measurements of weigh and volume and release checks. Ensure each cleaning meets standards set in SOP, records, and in accordance with GMP.
  • Observe in detail and report any process deficiencies, perform visual inspection of equipment for impurity and damage before and after cleaning.
  • Perform utility sampling and environmental monitoring as required and ensure the completion as adhered to schedule.
  • Provide guidance to technical staff on problem solving and trouble shooting.
  • Ensure area is inspection ready. Knowledgeable to guide inspectors.

Administration of Data Information for GP Production

  • Complete SAP transactions on a timely, accurate manner.
  • Perform Pharm net web activities.
  • Enter all data accurately and in timely manner such as Shop Floor Data, LIMs, Master, change request forms.

Process improvement and development

  • Assist implementation of facility, equipment, and process improvement projects
  • Assist in writing specifications, protocols and reports related to facility, equipment, and process improvement of production process
  • Modification of SOPs and BPRs for new processes in accordance with change control policies
  • Perform IQ, OQ, and PQ for new equipment
  • Attend meetings with other support functions representing production as needed

Preparation of Trending reports and SPC data analysis

  • Assist with implementation of corrective actions in production
  • Assist in CCR, CAPA as needed and manage them to completion as per committed due dates

Housekeeping

  • Participate in keeping the production area in a tidy, GMP manner, following 5S guideline (sort, straighten, shine, standardize, sustain)
  • Disinfect area as required in SOP.
  • Assist to ensure loading dock and hallways are clean and unobstructed by materials or equipment, garbage is discarded daily to designated area outside production.
  • Assist to ensure office area is kept in a tidy clean manner.
  • Supply airlock with gowning materials
  • Animate visual management tools
About You

Minimum Qualifications
  • Minim…
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary