Technologist Downstream

We’rean 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. Execute downstream processing, sterile filtration of drug substance

• Set up, maintain a variety of automated and manually operated equipment and perform production activities in downstream processes: clarification by centrifugation and TFF, purification by zonal centrifugation, splitting by continuous flow centrifugation, inactivation, diafiltration and sterile filtration of drug substance.

• Perform troubleshooting and assessment of processes and technical problems.

• Clean-in-place (CIP), cleaning-out-of-place (COP) of downstream equipment and vessels.

• Provide training to personnel.

• Execute and verify IQ/OQ/PQ validation and cleaning verification protocols. Ensure all equipment, instruments and systems are properly assembled, installed, tested and maintained.

• Participate in preventive maintenance of production equipment and instruments.

2. Perform sampling and analytical tests - utility sampling, environmental monitoring and area-specific testing

• Sample processed materials and perform in-process testing according to procedures.

• Deliver samples to other departments on site as required.

• Perform area-specific testing, utility sampling and environmental monitoring for production.

3. MaintenanceofCleanrooms,Equipment,Inspectionreadiness

• Perform routine cleaning and disinfection activities in classified environments.

• Maintain and organize cleanroom in good cGMP state and ensure area is always inspection ready.

• Submit equipment/material orders and maintain inventory of spare parts, purchasedmaterials fordownstream processing.

• Maintain safe and clean work environment by following site procedures and cGMP regulations.

• Participate in facility preparation and inspection readiness, safety and process audits.

4. Administrationofdatafordrugsubstanceoperations

• Document, review and maintain production and monitoring activities for drug substance manufacturing.

• Draft,reviewandrevisecGMPdocuments(SOPs/SWs,batchrecords, protocols,change controls,reports and other manufacturing supporting documents).

• Analyze, enter & verify data on paper based or electronic documents.

• FollowallSWls/SOPsandcomplytositepoliciesandprocedures.

5. Participate in continuous process and equipment improvement, Health, Safety & Environment. Quality, and Inspection readiness initiatives

• Perform and participate in continuous improvement and development projects.Support Deviations,CCR,CAPAinQualitysystemasneededandassist untilcompletionaspercommittedduedates.

• Participate in deviation investigations and root cause analysis.

• Follow HSE SOPs, identify and minimize risks, promote safety culture.

• Comply with HSE guidelines on the disposal of waste.

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

​Minimum Qualifications:

Education:

• Minimum 3 years College Diploma (Biochemistry, Microbiology, Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences), plus a minimum of 12 months of previous relevant work experience. 

• Preferred 4 years Bachelor's degree (Biochemistry, Microbiology,
  Bioengineering, Biotechnology, Chemistry, Chemical Engineering, Pharmaceutical Sciences), plus a minimum of 12 months of previous relevant work experience. 

Skills and Knowledge:

1.    Functional, Technical or scientific

• Purification Process.

• Production Equipment.

• Aseptic Technique.

• Current Good Manufacturing Practices (cGMPs).

• Knowledge and experience in Chemistry, Microbiology, Biochemistry.

• Mathematics, Computer, Mechanical Aptitude, Technical Writing, Quality and Improvement, Safety.

2. Supervisory, Managerial and Personal

• Communication I Networking

• Interpersonal / Teamwork

• Stress/Time Management

• Conflict Resolution

• Flexibility/ Adaptability

• Self-management

• Decision-making

• Creativity / Innovation

• Presentation

Hours Of Work:

• Training: Inclusive from Monday to Friday 08:00 AM - 16:00 PM

• Shift Schedule: Inclusive from Sunday to Thursday/Tuesday to Saturday/ Friday to Tuesday 6:00 AM -14:00 PM (Subject to change).

​

​This is subject to change at anytimeand it should not be construed as limiting the right of the company to make such a 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 yousubmityour Workday application, otherwise your application will not be considered for this position

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, whetherit’sthrough a promotion or lateral move, at home or internationally. 

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. 

• Takegood careof yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare,preventionand wellness program

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.

Pay rate - 48.02 per hour

AI Usage

"Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, toanalyzedata and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information toidentifypatterns, 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 concernregardingyour personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal,  Data Subject Rights Webform.TheData Subject Rights Webform can also be used to request 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 andretainhighly talentedemployees from diverse backgrounds, allowing us tobenefitfrom a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants.  Accommodations for persons with disabilitiesrequiredduring the recruitment process are available upon request. 

Thank you in advance for your interest.

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