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Added 13 mins ago
M
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- Full-time
Munters is a global leader in energy-efficient climate solutions for mission-critical processes. Our technology helps customers manage humidity, temperature, and energy use while reducing…
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Project Manager
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- Full-time
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Lead Consultant - Oracle Fusion HCM Cloud - Payroll
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Mississauga, ON
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At least 7 years of Information Technology experience.
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- $65,000 CAD / year
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Added 42 mins ago
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Added 42 mins ago
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Added 1 hour ago
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Supervisor, Centralized Scheduling
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Added 1 hour ago
Manager, Analytical R&D (Lab Automation)
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Toronto, ON · Etobicoke, ON
…environments. Organizes, coordinates and oversees NPD process in the team-based environment, provides technical guidance to senior scientists/chemists implements team-oriented approach from…
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Added 3 hours ago
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Added 3 hours ago
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Sr. Controls Programmer
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Toronto, ON
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Apotex

Manager, Analytical R&D (Lab Automation)

Toronto, ON, Canada
Etobicoke, ON, M9W 6Y3, Canada

The hiring range for this position is $109,933.56.14- $153,906.98 CAD per year.

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Job details

Pay: The hiring range for this position is $109,933.56.14- $153,906.98 CAD per year.
Experience: 7+ years of pharmaceutical industry experience with demonstrated achievements in pharmaceutical R&D with focus on analytical research.
Posting language: English
Posted: Sep 22, 2026

Original job description

About Apotex Inc.

Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.

For more information visit: www.apotex.com.

Job Summary

Responsible for directing the staff and activities of Analytical Research & Development To develop testing methods for drug substance and drug product. Advices the Product development group in the development of products through a thorough understanding of the chemistry of molecules in products and its behaviour in different dynamic environments. Organizes, coordinates and oversees NPD process in the team-based environment, provides technical guidance to senior scientists/chemists implements team-oriented approach from the earlier stages to completion of the project. Evaluates technical data and decides on course of action during NPD process. Ensures quality of the newly developed analytical methods and regulatory submission documents. Reviews/approves new product specifications. Provides expert advice to Formulation Development Department on critical quality attributes such as stability, compatibility, dissolution, and solubility to optimise and facilitate formulation development. Establishes close working relationships with other Product Development departments to create an integrated research environment and to ensure timely completion of NPD related submission documents for RA. Lends expertise to other areas within the Apotex organization. Assists Director in strategic planning, budgeting and staffing.

Job Responsibilities

Plans, organizes and oversees the activities in the Analytical R & D Team.
Manage effective method development and validation activities in the area of lab automation
Provide recommendations to the management on enhancing productivities by using advanced lab automation equipment.
Reviews and approves regulatory submission and other technical reports generated by the Analytical Development Team. Ensures the quality of documentation and test results generated in the AD.
Monitors the quality and productivity of the lab output to ensure that optimum levels are achieved. Makes recommendations to the Director for continuous improvement of lab operations.
Coordinates AD lab activities with those of other Analytical units
Liaises with the Formulation Development Department and provides input to the formula development process as related to drug product compatibility, stability and dissolution/drug delivery characteristics.
Works closely with other units of Analytical Operations, provides expert advice to other members of the AO team.
Liaises across the organization at all levels to provide an in-depth level of expertise.
Makes presentations at the executive level to keep them current with research and project development.
Liaises with relevant laboratories to ensure timely physical testing of pharmaceutical samples.
Investigates, encourages and uses unique problem solving techniques to perform trouble-shooting on highly complex issues with respect to the stability of drug substances and drug products, compatibility of API and excipients, chromatographic methodology.
Lends expertise to other Analytical groups for the resolution of more complex technical issues to ensure a holistic approach.
Recommends strategy and action plan with respect to new technology to Director, Analytical Development.
Continuously upgrades knowledge in pharmaceutical chemistry through review of scientific literature, attendance of training courses, and professional conferences.
Ensure proactive performance management of self and the team through regular performance discussions, annual performance reviews and career development.
Participate and lead performance conversations with employees, including monthly one on ones, to connect on performance; check in on employee’s progress toward achieving Objectives, offer support and remove barriers; and, communicate and revisit performance expectations to reinforce and encourage high performance culture and a safe working environment for all employees.
Utilize open, honest, two way communication to build trust-based relationships with employees, business partners and direct leader while continuously improving leadership capabilities by personally seeking feedback and development.
Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.
Utilize your networks to attract and hire talent in a comprehensive, differentiated and consistent manner essential to our continued growth; then, onboard new employees by providing a consistent experience that reflects the values and commitments made to candidates during the hiring process.
Ensure adherence of team members (direct reports) with all compliance programs and company policies and procedures.
All other duties as assigned.

Job Requirements

Education

Bachelors in Scientific discipline especially Organic Chemistry or Analytic Chemistry or pharmaceutical sciences. Masters or Ph.D. preferred.

Knowledge, Skills and Abilities

Advanced knowledge of analytical, organic and solid-state chemistry, pharmaceutical solid dosage forms.
In depth knowledge of regulatory guidelines (FDA, TPD, ICH etc.) GMP and GDP.
Excellent written and verbal communication skills.

Experience

7+ years of pharmaceutical industry experience with demonstrated achievements in pharmaceutical R&D with focus on analytical research.
Expertise in Drug substance and Drug product testing methods development.

At Apotex, we are committed to fostering a welcoming and accessible work environment, where everyone feels valued, respected, and supported to succeed.

We offer accommodation for applicants with disabilities as part of the recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require accommodation.

The hiring range for this position is $109,933.56.14- $153,906.98 CAD per year. The final agreed-upon salary may vary based on factors such as job-related knowledge, skills and experience.

We are looking for top talent. If your qualifications differ from those listed above, the scope of work and final agreed-upon salary may be adjusted to reflect your individual qualifications.

The Apotex Total Rewards package goes beyond base salary. Apotex offers bonus programs based on your position in the organization, you can excel based on our pay-for-performance philosophy. With comprehensive benefits, a pension plan to help you save for retirement and learning and development opportunities, we provide a comprehensive package for your personal and professional development.

Apotex will use artificial intelligence to screen, select and/or assess your application for this job.

This job posting is for a role that is currently available and vacant at Apotex.

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More about this job

Responsibilities

Direct and coordinate the Analytical R&D team, overseeing automated method development and validation, laboratory productivity, technical documentation, and regulatory submissions. Provide analytical expertise to product development and other departments, guide complex technical investigations, and lead team performance, development, and compliance.

Requirements

A bachelor's degree in a scientific discipline, particularly organic chemistry, analytical chemistry, or pharmaceutical sciences, is required; a master's or Ph.D. is preferred. Candidates need at least seven years of pharmaceutical industry experience in R&D, expertise in drug substance and drug product testing methods, advanced chemistry knowledge, and familiarity with regulatory guidelines and GMP/GDP.

Skills

Analytical Research And Development
Laboratory Automation
Analytical Method Development
Method Validation
Pharmaceutical Chemistry
Organic Chemistry
Solid-State Chemistry
Drug Substance Testing
Drug Product Testing
Regulatory Submissions
GMP
GDP
Stability Testing
Compatibility Testing
Dissolution Testing
Team Leadership

Benefits

Bonus Programs
Comprehensive Benefits
Pension Plan
Learning And Development Opportunities

Visa sponsorship

Not detected in the job text

Keywords

Analytical Research And Development
Laboratory Automation
Method Development
Method Validation
Pharmaceutical R&D
Pharmaceutical Chemistry
Organic Chemistry
Analytical Chemistry
Solid-State Chemistry
Drug Substance
Drug Product
Pharmaceutical Solid Dosage Forms
Regulatory Guidelines
FDA
TPD
ICH
GMP
GDP
Regulatory Submissions
Stability
Compatibility
Dissolution
Solubility
Chromatographic Methodology
Formulation Development
New Product Development
Quality Attributes
Technical Documentation
Performance Management
Continuous Improvement

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