CP

Contract Pharmaceuticals Limited

Verified Job Source

Dedicated To Making It Better

Mississauga, Ontario

Pharmaceutical Manufacturing
201–500 people

About

CPL is a leading contract development and manufacturing organization (CDMO) that provides development, manufacturing, packaging, and testing of non-sterile liquid and semi-solid pharmaceutical and regulated OTC products. We have two facilities located in Mississauga, Ontario, Canada including our manufacturing & development site and our QC/office site. Our site segregation and controls allow for the handling and processing of many specialized materials including flammable materials, light or oxygen sensitivity, and hormones. Our facilities are registered with the FDA and Health Canada and are routinely audited by regulatory agencies as well as our customers. By offering a full-spectrum partnership – from development to commercial production – CPL creates strategic relationships with our customers that creates mutual benefits.

Open positions

Process Engineering lll

On-site · Mississauga

The role involves providing technical process engineering expertise to support manufacturing, packaging, and maintenance departments while managing capital and continuous improvement projects. Responsibilities include executing qualification documents, leading strategic engineering projects, and providing senior technical guidance to production teams.

Compounder

On-site · Mississauga

The Compounder is responsible for manufacturing pharmaceutical products in compliance with SOPs, GMPs, and safety standards. Duties include weighing raw materials, operating and cleaning manufacturing equipment, and maintaining accurate production documentation.

Process Engineering lll

On-site · Mississauga

Provide senior technical process engineering expertise to support manufacturing, packaging, and maintenance departments. Manage capital and continuous improvement projects while ensuring compliance with GMP and validation standards.

Compounder

On-site · Mississauga

The Compounder is responsible for manufacturing pharmaceutical products in accordance with work orders, SOPs, and GMP standards. They must also perform equipment sanitation, handle raw materials, and maintain accurate documentation for all manufacturing activities.

Production Cleaner Technician

On-site · Mississauga

The Production Cleaner Technician is responsible for the independent disassembly, cleaning, and sanitization of packaging equipment to ensure compliance with SOPs and GMP standards. They also assist in the re-assembly of critical equipment and maintain cleanliness records for manufacturing and packaging areas.

Planner/Scheduler

On-site · Mississauga

The Planner/Scheduler is responsible for coordinating and planning short-term and long-term production schedules while performing necessary administrative support functions. They must also monitor order status, manage material requirements in SAP, and ensure production priorities are met efficiently.

Senior Manager, Financial Planning & Analysis

On-site · Mississauga

The Senior Manager will lead financial forecasting, budgeting, and cost analysis while partnering with cross-functional teams to drive profitability. They are responsible for managing the FP&A team, developing financial models, and providing actionable insights to senior leadership and the board.

Supplier Quality Specialist I

On-site · Mississauga

Responsible for the sampling and inspection of raw materials, packaging components, and consumable materials in compliance with cGMP standards. Manages third-party laboratory testing, including purchase order creation and the handling of retention samples.

Facilities Maintenance Technician I

On-site · Mississauga

The Facilities Maintenance Technician I is responsible for the operation, maintenance, and repair of building systems and utilities to ensure facility efficiency and safety. This role involves collaborating with cross-functional teams to maintain compliance with cGMP regulations and company policies.