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Added 17 mins ago
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Contract Pharmaceuticals Limited

Process Engineering lll (Packaging)

Mississauga, ON, Canada

$95,000 to $100,000 CAD / year · Contract

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Job details

Pay: $95,000 to $100,000 CAD / year
Job type: Contract
Apply by: Dec 5, 2026
Experience: Minimum 8 years relevant pharmaceutical experience in similar roles, with focus on production floor support, technology transfer and Continuous Improvement initiatives.
Posting language: English
Posted: Nov 5, 2026

Original job description

Job Type

Current Vacancy (12-month Contract)

Who We Are

At CPL, we are passionate about pharmaceutical product development and contract manufacturing. Our aim is to be the top choice CDMO in the non-sterile liquid and semi-solid pharmaceutical products domain and ultimately bring benefits to the customers using our manufactured products.

For more than 30 years CPL has partnered with the world’s leading pharmaceutical companies to provide full-service product development and manufacturing, singularly focused on innovation and efficiency.

We recognize our employees are our number one asset and support their career growth. We also offer a benefits program, deferred profit-sharing plan, paid time off, employee’s assistance program, work/life balance, employee recognition program, on-site parking, discounted gym membership.

Job Summary

Provide technical process engineering expertise to support Manufacturing, Packaging and Maintenance departments.

Manage manufacturing and packaging Capital and Continuous Improvement (CI) projects, including the introduction of new manufacturing and packaging technology, new processes and corresponding qualification/validation activities

Job Responsibilities

Actively supports the day-to-day operations of the Manufacturing, Packaging and Maintenance departments. Provides senior technical expertise and guidance in resolving issues and champions sustainable improvement opportunities.
Manages assigned critical capital projects, supports new product launches and is the voice of the Engineering department in all internal and external forums.
Prepares and executes qualification documents in accordance with GMP and CPL’s Validation Master Plan.
Develops and actively leads strategic Engineering projects using sound project management principles, including identification, justification, risk assessment, ROI, cost management, time management, scope management and resource management.
Prepares User Requirement Specifications (URS) for new equipment and participates in FAT (Factory Acceptance Testing) and installation processes.
Participates in the development of capital budgets, OPEX initiatives and prioritization of Continuous Improvement projects.
Generates manufacturing and packaging instructions for new/existing products and/or processes by adapting customer processes to CPL’s equipment and operational requirements through data obtained during line and process test runs. Uses gained knowledge to assist in the development and optimization of routings.
Provides senior engineering support and leads troubleshooting efforts on the production floor with the help of the Maintenance department.
Participates in customer process optimization and investigations, equipment selection and customer audits/visits.
Supports operation of Global Track & Trace functions at CPL from customer onboarding through to management of line-level systems / equipment.
Manages, documents and executes line trial activities.
Stay abreast of latest process technology developments. Contribute innovation and lean thinking into manufacturing and packaging processes.
Other duties as assigned.
Provide technical guidance to junior engineers.

Education

REQUIRED QUALIFICATIONS:

Bachelor’s Degree in an Engineering discipline.
Professional Engineer (P. Eng) designation preferred

Experience

Minimum 8 years relevant pharmaceutical experience in similar roles, with focus on production floor support, technology transfer and Continuous Improvement initiatives.

Knowledge, Skills, Abilities

Good understanding of relevant unit operations in the pharmaceutical industry, their capabilities and associated processes. High preference for liquid and semi-solid dose operations.
Working knowledge of automated / integrated production equipment and computerized systems.
Understanding of qualification and validation of equipment, facility and processes. Capable of writing qualification documentation with minimal supervision.
Proven ability to execute medium- to large-scale projects with minimal supervision.
Experience managing customers, vendors and contractors with minimal supervision/guidance.
High problem-solving capabilities, ability to address arising issues and make technical decisions within normally established guidelines with minimal supervision from management.
Good understanding of application of codes and regulations governing the implementation of process and equipment under OBC, OHSA, Fire Code and MOE.
Solid understanding of project management principles including project identification, justification, risk assessment, ROI, cost management, time management, scope management and resource management.
Proficiency in Microsoft Office applications including MS Project.
Excellent verbal and written English communication skills.
Demonstrated leadership capabilities/competencies, ability to manage teams and reach goals without formal reporting relationships.

Physical Demands/Working Conditions

Office environment (in person) and support in production area.
Occasional off-shift hours as needed to support production schedule

CPL is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. CPL is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us.

We thank all applicants for their expression of interest; however, only those selected for an interview will be contacted. No phone calls or agencies please.

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More about this job

Responsibilities

Provide senior process engineering support to manufacturing, packaging, and maintenance, including production troubleshooting, process optimization, and technical guidance. Lead capital and continuous improvement projects, product launches, equipment qualification and validation, line trials, and related customer and vendor activities.

Requirements

A bachelor’s degree in an engineering discipline is required, and a Professional Engineer designation is preferred. The role requires at least eight years of relevant pharmaceutical experience, strong knowledge of production operations, GMP qualification and validation, project management, and effective leadership and communication skills.

Skills

Pharmaceutical Process Engineering
Packaging Engineering
Production Floor Support
Technology Transfer
Continuous Improvement
Capital Project Management
GMP
Qualification And Validation
Troubleshooting
Process Optimization
Equipment Selection
Risk Assessment
Project Management
Factory Acceptance Testing
Microsoft Project

Benefits

Deferred Profit-Sharing Plan
Paid Time Off
Employee Assistance Program
Work-Life Balance
Employee Recognition Program
On-Site Parking
Discounted Gym Membership

Visa sponsorship

Not detected in the job text

Keywords

Pharmaceutical Manufacturing
Process Engineering
Packaging
Non-Sterile Liquids
Semi-Solid Products
Good Manufacturing Practice
Validation Master Plan
Qualification
Validation
Technology Transfer
Continuous Improvement
Capital Projects
Operational Expenditure
Factory Acceptance Testing
Equipment Installation
Line Trials
Process Optimization
Troubleshooting
Risk Assessment
Return On Investment
Project Management
Global Track And Trace
Automated Production Equipment
Computerized Systems
Microsoft Office
Microsoft Project
Ontario Building Code
Occupational Health And Safety Act
Fire Code

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