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Added 3 mins ago
RM
Supervisor, Centralized Scheduling
Ross Memorial Hospital
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- Full-time
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CE
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Added 1 hour ago
TP
Supervisor, Microbiology
Teva Pharmaceuticals
Toronto, ON
- Full-time
We are seeking an experienced Microbiology Supervisor to lead our Quality Control Microbiology Laboratory. In this role, you will oversee microbiological testing activities in support of…
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Teva Pharmaceuticals

Supervisor, Microbiology

Toronto, ON, Canada

The typical hiring range for this position is $92,560-$115,700. · Full-time

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Job details

Pay: The typical hiring range for this position is $92,560-$115,700.
Job type: Full-time
Apply by: Nov 28, 2026
Experience: Minimum 8 years of experience in a pharmaceutical microbiology laboratory.
Posting language: English
Posted: Oct 29, 2026

Original job description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

We are seeking an experienced Microbiology Supervisor to lead our Quality Control Microbiology Laboratory. In this role, you will oversee microbiological testing activities in support of commercial and stability products while ensuring compliance with GMP, GLP, and regulatory requirements. You will provide technical leadership to a team of microbiologists, drive continuous improvement initiatives, and serve as a key subject matter expert for microbiology-related operations and inspections.

How You’ll Spend Your Day

Lead and develop a team of microbiologists through coaching, mentoring, performance management, and training.
Oversee microbiological testing activities including:
- Non-sterile pharmaceutical product testing
- Environmental monitoring
- Antimicrobial effectiveness testing
- Microbial identification using compendial and in-house methods
Review and approve laboratory data, reports, investigations, deviations, and change controls.
Ensure data integrity and compliance through adherence to ALCOA+ principles and robust documentation practices.
Support and lead laboratory investigations, troubleshooting activities, and root cause analyses.
Act as the microbiology subject matter expert during regulatory inspections and customer audits.
Collaborate cross-functionally with Quality Assurance, Manufacturing, Regulatory Affairs, and other Quality Control teams.
Drive laboratory process improvements, compliance initiatives, and operational excellence projects.
Manage laboratory resources, supplies, and scheduling to support manufacturing and product release timelines.
Promote a strong culture of safety, compliance, and continuous improvement.

Your Skills And Experience

Bachelor's degree in Microbiology or a related scientific discipline.
Advanced degree is considered an asset.
Minimum 8 years of experience in a pharmaceutical microbiology laboratory.
Previous people leadership or supervisory experience.
Experience supporting regulatory inspections and audits.
Strong knowledge of pharmaceutical microbiology principles and compendial standards (USP, EP, JP).
Experience with microbiological testing methods and laboratory instrumentation, including:
- Endotoxin testing systems
- Microbial identification platforms (e.g., Vitek, Biolog, Omnilog)
- Autoclaves and sterility isolators
Thorough understanding of GMP, cGMP, and GLP requirements.
Strong knowledge of data integrity and quality systems.
Proven leadership and team development capabilities.
Excellent analytical, troubleshooting, and problem-solving skills.
Strong written and verbal communication skills.
Experience writing and reviewing SOPs, investigations, technical reports, and quality documentation.
Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.
Proficiency with Microsoft Office applications and laboratory information systems (LIMS).

How We’ll Take Care Of You

At Teva Canada we provide a rewarding and collaborative work experience, with career growth and development opportunities for employees, in a safe and caring environment! The typical hiring range for this position is $92,560-$115,700. The base pay offered may vary depending on job-related knowledge, skills, experience, education, and internal equity. In addition to base salary, this role may qualify for an annual bonus based on employment type. Certain positions may also be eligible for a sales commission structure as part of the overall compensation package. Beyond base pay, Teva also offers a comprehensive suite of wellness and benefits programs tailored to role and employment type, that continue to rank among the best in our industry! Our competitive offerings are designed to provide flexibility, security, and meaningful choices, empowering employees to thrive both personally and professionally throughout their journey with us.

As part of our commitment to well-being, employees may have access to:

Teva Canada’s choices Benefit Plan including Health, Dental, Disability, Life Insurance
Employee Assistance Program & Virtual Health Programs
Retirement Savings Programs
Employee Stock Purchase Plan (ESPP)
Time for yourself or those you care about, through paid time for Vacation, Wellness days, Care/Sick days, Teva Days and Volunteer Days
Education Assistance Program
Recognition programs such as Employee Service Awards
Employee Discounts
And much more!

More exciting details on the specific total rewards offerings to be provided at the offer stage depending on the position and employment type hiring for. This position will fill a current vacancy and Teva Canada may use an artificial intelligence (AI) system to assist with the initial screening and evaluation of job applications by analyzing for relevant skills, professional experience, and education, that best match the posted job qualifications. It is important to note that all final decisions in this process are made by a member of the hiring team.

Already Working @Teva?

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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More about this job

Responsibilities

Lead and develop the Quality Control Microbiology Laboratory team, overseeing microbiological testing, data review, investigations, and compliance with GMP, GLP, and regulatory requirements. Serve as the microbiology subject matter expert during inspections and audits, collaborate across functions, and drive laboratory improvements while managing resources and schedules.

Requirements

A bachelor's degree in microbiology or a related scientific discipline is required; an advanced degree is an asset. Candidates need at least eight years of pharmaceutical microbiology laboratory experience, supervisory or people leadership experience, inspection and audit support experience, and strong knowledge of compendial standards, laboratory methods, quality systems, and data integrity.

Skills

Microbiology Laboratory Leadership
Pharmaceutical Microbiology
GMP, cGMP, and GLP Compliance
Microbiological Testing
Environmental Monitoring
Antimicrobial Effectiveness Testing
Microbial Identification
Data Integrity and ALCOA+
Laboratory Investigations
Root Cause Analysis
Regulatory Inspections and Audits
SOP and Technical Documentation
Team Development
Quality Systems
LIMS

Benefits

Health Insurance
Dental Insurance
Disability Insurance
Life Insurance
Employee Assistance Program
Virtual Health Programs
Retirement Savings Programs
Employee Stock Purchase Plan
Paid Vacation
Wellness Days
Sick Days
Volunteer Days
Education Assistance
Employee Recognition Programs
Employee Discounts

Visa sponsorship

Not detected in the job text

Keywords

Quality Control Microbiology
Pharmaceutical Manufacturing
GMP
cGMP
GLP
USP
EP
JP
ALCOA+
Environmental Monitoring
Antimicrobial Effectiveness Testing
Endotoxin Testing Systems
Vitek
Biolog
Omnilog
Autoclaves
Sterility Isolators
LIMS
Microbial Identification
Stability Testing
Data Integrity
Root Cause Analysis
Change Controls
Deviations
Regulatory Inspections
Customer Audits
SOPs
Laboratory Investigations
Microsoft Office
Continuous Improvement

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