A career at Resilience is more than just a job – it’s an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit www.resilience.com

The Specialist, Manufacturing performs upstream and downstream manufacturing operations in a cGMP biopharmaceutical environment. Operating under the guidance of the Supervisor, Manufacturing, this role supports both clinical and commercial production, ensuring all operations are conducted in strict accordance with safety, quality, and regulatory standards. Responsibilities include executing batch activities with high precision, maintaining rigorous documentation, and contributing to site-wide continuous improvement and safety initiatives.

Job Responsibilities
Operations

Operates manufacturing equipment and performs associated processing operations, including:

Bioreactors, centrifuge, Bio Safety Cabinets (BSC)

Chromatography skids

UF/DF, TFF systems, as well as nanofiltration systems

Performs filtration using various methods and filter sizes

Proficient in aseptic techniques and practices allowing for contamination control in manufacturing spaces.

Executes CIP/SIP (Clean-in-Place/Steam-in-Place) on process skids and vessels

Performs in-process sampling and basic analytical tests

Participates in upstream and downstream manufacturing operations across the production process.

Utilizes HMIs and computerized systems to operate various skids and production equipment.

Compliance & Documentation

Performs all duties according to the SOPs/WINs and cGMPs and all other established safety standards and company policies.

Maintains housekeeping standards in the manufacturing area including cleaning of the process suites as guided by internal procedures.

Documents and records all necessary information/data as per SOPs/WINs and cGMPs requirements.





Quality & Continuous Improvement

Identifies and escalates product/material defects, process deviations, or equipment issues to Management.

Supports continuous improvement initiatives by identifying and communicating process, equipment, or documentation issues to Management.

Training & Development

Acquire and maintain all required certifications and qualifications for the assigned work area, including visual inspection qualification and cold room training.

Cross-train and support other work areas as needed.

Minimum Qualifications
Experience & Education

Demonstrated understanding of cGMP documentation requirements, data integrity principles, and regulated manufacturing procedures.

Ability to operate bioprocessing equipment and execute procedures (CIP/SIP, filtration, materials receipt/FIFO) following approved SOPs/WINs.

Ability to recognize routine process or equipment issues and confer with Management to confirm the appropriate course of action.

Preferred Qualifications

Bachelor's Ddegree or Technical Diploma in Biochemistry, Biotechnology, Biology, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with exposure to bioprocessing techniques through coursework, co-op, or internship.

2+ years of experience in a biopharmaceutical, pharmaceutical, or CDMO manufacturing environment, ideally in upstream or downstream processing.

Hands-on experience operating chromatography systems (AKTA Ready or equivalent), cross-flow filtration (UF/DF/TFF), nanofiltration, and bioreactors.

Physical & Work Environment

Work will involve extended hours, including evenings and weekends, depending on project deadlines and operational needs.





Adhere to EHS policies, procedures, and standards, ensuring hazards are identified and risks are minimized to maintain a protected work environment

Physical demands may include standing for extended periods, ability to lift up to 20 KG, and working in cleanroom environments with appropriate gowning requirements.

Required to wear Personal Protective Equipment (PPE), including a fitted respirator; facial hair must not interfere with the face seal of a respirator in accordance with applicable safety standards and fit-test requirements.

Production suite (fFloor, walls, and ceiling) must be cleaned as per required frequency based on approved procedure.

Use of extendable mop handle as per approved procedures might be required based on production suites dimension.

Requires pushing buffer drums/totes.

Work Schedule
Work schedule operates on a rotating shift that may include 8-hour rotating shifts (day, afternoon, and night) or 12-hour rotating shifts (day or night), based on business and operational requirements.

Resilience Biotechnologies Inc. (RESILIENCE), is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). Requests for accommodation can be made at any stage of the recruitment process. Applicants are asked to make their needs/requirements known to Human Resources.

Benefits

annual cash bonus program

RRSP/DPSP with a generous company match

very competitive healthcare

dentalcare

vision care

life

LTD

AD&D; benefits package

fertility healthcare

family-forming benefits

paid vacation

paid holidays

pregnancy and parental leave top-up plan

tuition reimbursement

employee referral program

Our target base pay hiring range for this position is $24.00 - $34.50 per hour. Actual base pay is dependent on a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge.

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📌 Specialist, Manufacturing (Ontario)
🏢 Resilience
📍 Ontario