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Supervisor, Microbiology
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Jubilant Pharma Limited

Supervisor, Microbiology

Greater Montreal Metropolitan Area, QC, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Dec 12, 2026
Posting language: English
Posted: Nov 12, 2026

Original job description

Job Description

Job Title: Supervisor, Microbiology

Req Id: 1928

Posting Start Date: 11/2/26

Job Description:

About Jubilant Radiopharma

At Jubilant Radiopharma, we help healthcare professionals deliver essential patient care through radiopharmaceutical solutions. Our team is driven by quality, safety, innovation, and collaboration. We foster an environment where everyone can contribute, grow, and make a meaningful impact.

Role Overview

We are seeking an experienced leader to oversee microbiology activities at our Kirkland facility. In this role, you will provide leadership for microbiology laboratory operations, regulatory compliance, scientific excellence, and team development while supporting continuous quality improvement initiatives.

You will play a key role in environmental monitoring, contamination control, microbiological investigations, and the assessment of potential impacts on finished products and manufacturing environments.

Key Responsibilities

Lead the day-to-day operations of the microbiology laboratory and support the development of a high-performing team.
Ensure analytical accuracy and compliance with GMP, cGMP, and applicable regulatory requirements.
Write, review, and approve impact assessments, protocols, reports, and microbiological procedures.
Support microbiological method development, transfer, and validation activities.
Manage laboratory equipment and ensure proper qualification, calibration, and maintenance.
Establish, maintain, and continuously improve the Environmental Monitoring (EM) program in accordance with internal and regulatory standards.
Oversee testing of finished products, raw materials, and stability samples.
Serve as the microbiology subject matter expert during regulatory inspections and audits (Health Canada, FDA, EMA).
Lead or support investigations related to Out-of-Specification (OOS) results, quality events, and contamination issues.
Identify root causes and implement effective corrective and preventive actions.
Ensure personnel qualification for cleanroom access and compliance with microbiological best practices.
Provide technical support to Production, Quality Assurance, and Validation teams.
Support new product introductions, site transfers, and continuous improvement initiatives.
Review microbiological trends and generate reports to support data-driven decision making.
Participate in recruiting, training, and developing microbiology team members.

Qualifications

B.Sc. or M.Sc. in Microbiology or a closely related discipline.
Minimum ten (10) years of relevant experience in a pharmaceutical microbiology laboratory.
Experience working in a sterile environment.
Minimum five (5) years of relevant supervisory experience within a pharmaceutical microbiology laboratory.
Excellent knowledge of environmental monitoring programs.
Experience managing aseptic operations for injectable sterile products.
Strong knowledge of microbiology laboratory operations and instrumentation.
In-depth knowledge of cGMP regulations applicable to sterile parenteral products in Canada, the United States, and the European Union.
Knowledge of microbiology analytical development, method transfer, and validation.
Proficiency with Microsoft Office and SAP.
Bilingual in French and English. Proficiency in English is essential since the position requires interaction with regulatory agencies outside Quebec (e.g., the FDA)
Strong interpersonal, organizational, communication, and technical writing skills.
Demonstrated ability to manage multiple priorities and concurrent projects.

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More about this job

Responsibilities

Lead microbiology laboratory operations, environmental monitoring, testing, and regulatory compliance, while overseeing investigations and contamination-control activities. Develop the microbiology team, provide technical support across departments, and drive continuous improvement and data-informed decisions.

Requirements

Requires a B.Sc. or M.Sc. in microbiology or a related discipline, at least 10 years of pharmaceutical microbiology experience, and at least 5 years of supervisory experience. Candidates must have sterile-environment and injectable-product experience, strong knowledge of environmental monitoring and cGMP requirements, proficiency with Microsoft Office and SAP, and be bilingual in French and English.

Skills

GMP Compliance
Environmental Monitoring
Contamination Control
Aseptic Operations
Sterile Product Testing
Method Development
Method Transfer
Method Validation
Root Cause Analysis
Corrective And Preventive Actions
Laboratory Equipment Qualification
Regulatory Inspections And Audits
Team Leadership
Technical Writing

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical Microbiology
GMP
cGMP
Environmental Monitoring
Contamination Control
Sterile Parenteral Products
Injectable Products
Aseptic Operations
Microbiological Testing
Finished Product Testing
Raw Materials
Stability Samples
Microbiological Method Development
Method Transfer
Method Validation
Out-Of-Specification Results
Quality Events
Root Cause Analysis
Corrective And Preventive Actions
Cleanroom Qualification
Laboratory Instrumentation
Equipment Qualification
Calibration
Health Canada
FDA
EMA
Microsoft Office
SAP
Regulatory Audits
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