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Catalent Pharma Solutions

Production Supervisor

Strathroy, ON, Canada
CAN-Strathroy ON Adair, Canada

The final salary offered to a successful candidate may vary within this range $65,000 – $80,000, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. · Full-time

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Job details

Pay: The final salary offered to a successful candidate may vary within this range $65,000 – $80,000, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc.
Job type: Full-time
Apply by: Oct 26, 2026
Education: High school diploma
Experience: Minimum 3+ years of experience leading and supervising a team in a manufacturing environment, ensuring safety, quality, and productivity.
Posting language: English
Posted: Oct 7, 2026

Original job description

About Site

The newly launched manufacturing facility on Adair Blvd marks a pivotal expansion of Catalent’s Zydis® technology, a globally renowned, fast-dissolve oral dosage form that has transformed the lives of millions of patients worldwide. This is your opportunity to join a dedicated team at the forefront of pharmaceutical manufacturing. At Adair, you’ll play a vital role in the startup of a site built for innovation and excellence, from installation and qualification to regulatory approval and commercial manufacturing.

Position Summary

We have an opportunity for a Production Supervisor to join our team reporting directly to the Site Director. This role plays a key part in ensuring the safe and efficient production of high-quality pharmaceutical products while maintaining strict compliance with regulatory standards. You will lead and empower your team to achieve operational excellence and continuous improvement. This position offers the chance to contribute to a growing facility dedicated to innovation and quality.

Shift: Monday-Friday 8 AM-4:30 PM; Transition to 12-hour shifts in the future Location: Adair, ON 100% Onsite

The Role

Meet daily production objectives and manage each shift to ensure production efficiency, optimizing the use of resources, labor, equipment, and materials.
Supervise a team of hourly employees with a strong focus on engagement and performance.
Ensure compliance with safety, quality, efficiency, uptime, cost, and Quality Control objectives, as well as adherence to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs).
Assist in troubleshooting and investigations to address off-standard results.
Maintain safety, health, and environmental procedures, identifying and correcting potential issues while driving continuous improvement through Risk Assessment strategies.
Schedule manpower, machinery, and materials to meet or exceed budget requirements, resolving work problems and recommending productivity and quality improvements.
Work extended hours or weekends as needed to meet deadlines or address operational issues.
Perform other duties as required.

The Candidate

Minimum Requirements

High School Diploma, GED/CAEC and/or educational credential assessment (ECA) is required.
Minimum 3+ years of experience leading and supervising a team in a manufacturing environment, ensuring safety, quality, and productivity.
Excellent leadership, communication, and interpersonal skills to manage a diverse workforce and foster a culture of continuous improvement.
Must be clean shaven to wear a respirator, as required by Health & Safety standards.
Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
Currently, Catalent participates in the Ontario Immigrant Nominee Program (OINP) on a limited basis.
Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency through the Alliance of Credential Evaluation Services of Canada (ACESC), such as World Education Services (WES).
The employee's role frequently involves sitting and utilizing hands and fingers for tasks such as handling, feeling, and keyboard manipulation, necessitating manual dexterity. Occasionally, the position requires standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, alongside close vision capabilities and potential exposure to chemicals.

Preferred Skills & Background

Bachelor’s degree in a relevant field such as Life Sciences, Engineering, or a related discipline preferred. Equivalent education and experience may be considered.
Strong commitment to workplace safety and a thorough understanding of occupational health and safety regulations in Ontario.
Strong analytical and problem-solving skills to identify and resolve production issues, optimize processes, and drive continuous improvement.
Excellent written and verbal communication skills to collaborate effectively with cross-functional teams including quality control, supply chain, and engineering.
Strong organizational and time management skills to prioritize tasks, allocate resources effectively, and meet production schedules.
Proficiency in Microsoft Office Suite (Outlook, Excel, PowerPoint, Word).

Pay

Why You Should Join Catalent

Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance)
Group Retirement Savings – Registered Pension Plan (RPP) with employer contributions
Employee Reward & Recognition programs
Opportunities for professional and personal development & growth including tuition reimbursement

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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More about this job

Responsibilities

The Production Supervisor will manage daily production objectives and lead a team of hourly employees to ensure operational efficiency and compliance with GMP standards. They are responsible for troubleshooting production issues, maintaining safety protocols, and driving continuous improvement initiatives within the facility.

Requirements

Candidates must have a high school diploma or equivalent and at least 3 years of experience leading a team in a manufacturing environment. Strong leadership, communication, and problem-solving skills are required, along with the ability to work in a clean-shaven environment for respirator use.

Skills

Production supervision
Pharmaceutical manufacturing
GMP compliance
SOP adherence
Team leadership
Continuous improvement
Risk assessment
Troubleshooting
Resource management
Operational excellence
Safety management
Microsoft Office Suite
Analytical skills
Problem-solving
Time management
Communication

Benefits

Health insurance
Dental insurance
Vision insurance
Life insurance
Group retirement savings
Registered pension plan
Employee reward and recognition programs
Tuition reimbursement

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical manufacturing
Zydis technology
GMP
SOP
Production supervision
Risk assessment
Continuous improvement
Quality control
Supply chain
Engineering
Microsoft Office
Operational excellence
Safety standards
Regulatory compliance
Manufacturing facility
Resource optimization
Performance management
Troubleshooting
Health and safety
Workforce management

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