Technical Administrator

BioTalent Canada; Toronto; Presencial; CAD 70.000 - 110.000; Jornada completa

Descripción de la vacante

Sanofi in Canada seeks a production specialist to support downstream CP production, purification and data management within GMP-compliant operations. You will assist with SOP reviews, equipment operation, SAP data entry and process improvements in a fast-paced biopharma setting.

Responsibilities include training staff on cGMP/HSE, coordinating CP activities, and preparing trending reports while ensuring inspection readiness and SCR compliance. Monday to Friday schedule.

Formación

• Bachelor’s degree (Biochemistry, Microbiology, or Bioengineering) and relevant experience.
• Master’s degree (preferred) with additional years of applicable work experience.

Responsabilidades

• Assist in review SOPs, logbooks, and GMP-compliant documentation.
• Train staff to follow cGMP, HSE and SOP requirements.
• Coordinate CP department activities and participate in daily meetings.
• Operate centrifuges and chromatography for CP antigens purification.
• Complete SAP transactions and input data accurately.
• Support facility, equipment, and process improvement projects.
• Prepare trending reports and SPC data analyses.

Conocimientos

Microbiology knowledge

Fermentation knowledge

Mechanical skills

Technical writing

Problem solving

Troubleshooting

Educación

Bachelor’s degree in Biochemistry, Microbiology, or Bioengineering

Master’s degree in Biochemistry, Microbiology, or Bioengineering (preferred)

Herramientas

SAP

Visio

AutoCad

MS Access

JMP

Descripción del empleo

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

1. 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.
• Coordinate activities within CP department (Adsorptions, Upstream and MWS).
• 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.

3. 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.

4. 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.

5. 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.

6. 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.
• 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 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.

No employee has a proprietary right to an activity or group of activities.

Activities may be changed or reassigned to meet the needs of the operations.

About You

Education

• Minimum four (4) years bachelor’s degree (Biochemistry, Microbiology, Bioengineering), plus a minimum of four (4) years of previous relevant work experience.
• Preferred two (2) years master’s degree (Biochemistry, Microbiology, Bioengineering), plus a minimum of three (3) years of previous relevant work experience.

Skills and Knowledge

1. Functional, technical or scientific

• Sound knowledge of Microbiology.
• Sound knowledge of Fermentation.
• Basic mechanical skill and knowledge.

2. Supervisory, Managerial and Personal

• SAP, Visio, AutoCad, MS Access, JMP.
• Technical writing.
• Problem solving, trouble shooting.

Inclusive from Monday to Friday 8:00 AM – 4:00 PM.

This is subject to change at any time and it should not be construed as limiting the right of the company to make such a change to meet the requirements of the operation.

Applications received after the official close date will be reviewed on an individual basis.

This position is for a current vacant role that is now open for applications.

Why Choose Us

• Bring the miracles of science to life alongside a supportive, future‑focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well‑crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high‑quality healthcare, prevention and wellness program

AI Usage

“Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision‑making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company’s Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal,can also be used torequest access or correction of your personal information and file a complaint.

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.

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.

Join Sanofi and step into a new era of science – where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never‑been‑done‑before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.