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Catalent Pharma Solutions

Process Technician

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

The start hourly rate for this position is $26.93/Hr. · Full-time

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Job details

Pay: The start hourly rate for this position is $26.93/Hr.
Job type: Full-time
Apply by: Oct 26, 2026
Education: High school diploma
Posting language: English
Posted: Sep 28, 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 Process Technician to join our team. In this role, you will develop skills in your primary area and a secondary area, becoming a specialist in one and supporting others. You will assist in maintaining production schedules, ensuring compliance with safety and quality standards, and supporting continuous improvement initiatives. This position offers the chance to work in a dynamic environment where your contributions directly impact the success of our operations.

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

The Role

Minimise equipment downtime and improve equipment availability by being accountable for delivering and reducing machine turnaround time.
Ensure the team consistently sets and upholds site safety best practices by demonstrating zero-tolerance behaviors, continually challenging and raising safety standards, and eliminating risk to employees, products, and the environment through active participation in safety and accident investigations and completion of high-quality, current risk assessments.
Ensure team consistently sets site quality best practices by demonstrating zero defect behaviour, continually challenging and raising Quality standards.
Ensure batch manufacturing records are accurately completed in real time to support timely documentation approval, with processes and procedures including online and in‑process quality checks - followed rigorously to deliver consistent, high‑quality products, while ensuring all team members adhere to SOPs and comply with individual cGMP responsibilities to prevent any deficiencies.
Carry out specific targeted training as required, and ensure Compliance Wire training requirements are carried out within specified due dates
Recommend improvements to the batch manufacturing process, SOP’s to increase process efficiency and effectiveness and maintain 5S and continuous improvement activities.
Ensure that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Catalent values.
Perform other duties as assigned.

The Candidate

Minimum Requirements

High School Diploma, GED/CAEC and/or educational credential assessment (ECA) is required
2 years or more of experience in a manufacturing environment is preferred
GMP work experience preferred
Pharmaceutical Manufacturing experience is an advantage
This role requires being clean shaven to wear a respirator, which is mandatory to meet Health & Safety requirement
Frequent standing, walking, climbing ladders/steps, reading written documents, and use of a computer monitor, as well as talking and listening; occasional stooping, kneeling, crouching, bending, carrying, reaching with hands and arms; occasional lifting and/or moving up to 25 kg; and may be exposed to inclement weather or required to work in environments that require the use of protective gear and heightened awareness of personal and others’ safety.

Preferred Skills & Background

Good math skills and ability to operate related computer applications
Ability to work independently and complete daily activities
Strong teamwork, clear communication, and effective listening skills
Good standard of oral and written English and ability to follow written instructions
Able to complete written batch records
Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency as determined by the Alliance of Credential Evaluation Services of Canada (ACESC) such as WES
This position does not qualify for sponsorship

Pay

The start hourly rate for this position is $26.93/Hr. Catalent is a global employer, and this compensation does not reflect positions that work in other countries.

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 Process Technician will maintain production schedules and ensure compliance with safety and quality standards while minimizing equipment downtime. They are responsible for accurately completing batch manufacturing records and supporting continuous improvement initiatives within the facility.

Requirements

Candidates must have a High School Diploma, GED, or equivalent, with at least 2 years of experience in a manufacturing environment. Experience in GMP and pharmaceutical manufacturing is preferred, and the role requires the ability to wear a respirator.

Skills

Pharmaceutical Manufacturing
GMP Compliance
Equipment Maintenance
Batch Manufacturing Records
SOP Adherence
Safety Standards
Quality Control
Continuous Improvement
5S Methodology
Technical Documentation
Computer Literacy
Teamwork
Communication Skills
Risk Assessment

Benefits

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Group Retirement Savings
Registered Pension Plan
Tuition Reimbursement
Professional Development

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical Manufacturing
GMP
Zydis Technology
Process Technician
Batch Manufacturing Records
SOP
5S
Continuous Improvement
Safety Standards
Quality Assurance
Equipment Maintenance
Risk Assessment
Compliance Wire
Manufacturing Facility
Oral Dosage Form
Respirator
Documentation

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