About Bora

Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora’s teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer’s success more certain.

Position Status

This is a permanent fulltime position. This job posting reflects a current vacancy within the organization. The position is active, approved, and intended to be filled as part of our staffing needs. This posting is for an existing and currently open position.

General Description
Perform microbiological analyses on raw materials, finished products and environmental monitoring samples.

Key Responsibilities

• Perform microbial method validation of raw materials and finished products within defined project timelines. This includes writing of test protocols and reports, setting up tests, transfers and reading plates using aseptic technique.
• Maintain QC laboratory equipment performance: Perform assigned laboratory duties; maintain equipment according to SOPs & manufacturers’ guidelines.
• Maintain quality results: Perform tests according to quality & customer service standards; document results according to cGMP standards; assist in investigations of OOS results by problem solving & troubleshooting; write minor deviations; ensure compliance to cGMP; write investigation reports; assist in regulatory & corporate audits; conduct & participate in self-inspections.
• Complete operational requirements as per schedule: Attend daily meetings; support process validation; implement efficiencies to improve productivity; review QC procedures; implement new procedures; maintain QC laboratory supplies inventory.
• Implement new programs, tests methods, instrumentation, & procedures: Prepare proposals; initiate change proposals; write justifications & feasibility reports; perform parallel testing; evaluate new methods.
• Maintain a safe & healthy work environment: Follow all safety policies; maintain a clean & orderly work area; report any potentially unsafe conditions within the workplace.
• Perform all work according to cGMP and following regulatory and Bora's standards, including thorough documentation and prompt reporting of any anomalies.
• Maintain laboratory systems and participate in projects as required.
• Working closely with others in the group to achieve business objectives.

Experience and Skills

• Minimum of 2 years of Quality Control microbiology experience in pharmaceutical laboratory environment.
• Good theoretical and practical knowledge of microbiological techniques.
• Knowledge of Microbial IDs and investigations.
• Demonstrated computer proficiency in LIMS, SAP and Excel.
• Good knowledge of laboratory GMP and the Pharmacopoeias.
• Good verbal and written communication skills.
• Works well in a fast-paced team environment and individually.
• Ability to manage multiple projects and tasks concurrently and effectively.

Education

Required: College Diploma in Microbiology or a related science.

Preferred: University degree in Microbiology.

Working Conditions

• Onsite role.
• Working within the microbiology laboratory with raw materials, finished products and environmental samples.
• Exposure to and handling of biological cultures as part of routine laboratory activities.
• Standard 37.5-hour work week.
• May be required to work shifts/weekends.

Additional Information

In accordance with Ontario’s pay transparency requirements, candidates will be notified when they are no longer under consideration or once the vacancy is closed. Updates regarding application status may be communicated via email or through the online applicant profile, where applicable.

As part of our recruitment process, we may use technology-assisted tools, including automated systems, to support the review and assessment of applications. These tools do not make final hiring decisions. All decisions related to screening, interviewing, and selection are made by our Talent Acquisition and hiring teams.

Compensation Range

$46,430 - $58,040

Benefits Include:

We offer a comprehensive benefits package designed to support our employees’ wellbeing, including:

• Competitive salary and performance-based incentives

• Comprehensive health coverage including medical, dental, and vision insurance

• Retirement savings plans with employer contributions

• Paid time off and flexible work arrangements

• Professional development opportunities

• Employee wellness programs and resources

• Employee Assistance Program and Mental Health Resources

At Bora, our values guide everything we do — from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone.
We’re proud to be an equal opportunity employer, committed to building a diverse and inclusive workplace where everyone feels empowered to contribute and grow. We welcome applications from qualified individuals of all backgrounds, experiences, and perspectives.

If you require accommodation during any stage of the application or interview process, or if you’d like to learn more about our accessibility policies, please contact us at accessibility@bora-corp.com.