Technical Administrator Job Toronto area,Ontario Canada,Manufacturing / Production

Reference no: R2871008

Position title:

Technical Administrator Duration:
Fixed Term Contract - 3 years

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 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. 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:

Administration of Downstream production activities Assist in review BPR, SOP, logbooks, and monitoring charts for completion and insurance of accuracy of all documents as per GMP guidelines. Train technical staff comply to cGMP, HSE and SOP requirements. Participate in daily meetings and report findings to management. Participate in deviation investigations. Coordinate activities within CP department (Adsorptions, Upstream and MWS).

Health, Safety, Environment Wear proper PPE when performing tasks. Drive culture of HSE in department. Escalate any potential hazards. Help develop proposed solutions. Participate in HSE checks and inspections. Follow safety procedures.

Purification and Sterile Filtration of CP antigens Operation of Centrifuges for precipitation purification of CP antigens. Operation of column chromatography for isolation of CP antigens. Operation of Ultrafiltration units used for processing CP antigens. Sterile filtration of CP antigens using aseptic technique and tube welder. Perform and prepare for analytical tests such as lowry, Bradford and SDS-PAGE. Assist in problem solving and trouble shooting.

Ensure area is inspection ready. Knowledgeable to guide inspectors.

Administration of Data Information for CP Production Complete SAP transactions on a timely, accurate manner. Perform Pharm Net Web activities. Enter all data in a timely, accurate 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 execution and writing of documents (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 with CCR, CAPA as needed until completion as per committed due dates.

Housekeeping Participate in keeping the production area tidy, in a 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…