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 advantages 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:

To disassemble, clean and re-assemble packaging equipment ensuring that all packaging equipment and packaging lines are cleaned and sanitized according to the relevant Standard Operation Procedures SOPs. This is to ensure that cross contamination or bacterial contamination does not occur during the manufacturing and packaging process.

JOB RESPONSIBILITIES:

- Independent dis-assembly of all equipment and hardware in the equipment train.
- Independent cleaning of all equipment and hardware in the equipment train.
- Independent re-assembly of all equipment and hardware in the equipment train except for equipment deemed critical.
- Assisting the Mechanic lead in the re-assembly of primary filling equipment or equipment deemed critical. For example, filling machine nozzles and pumps.
- Independent cleaning and sanitizing of related wash up areas, filling and packaging rooms and lines.
- Ensure packaging equipment is cleaned and sanitized according to the specified cleaning SOPs and documented accordingly.




- Responsible for working in compliance with established safe work practices and procedures; using personal protection and safety equipment as required.
- Report any injury or illness immediately and notifies CPL of any hazards, unsafe acts or conditions in the workplace.
- Maintain the wash-up areas to ensure that it meets GMP Standards at all times.
- Maintain cleanliness of the Packaging and Manufacturing rooms and equipment storage rooms.
- Maintain cleaning records.
- Ensure that the correct cleaning supplies and sanitizing solutions are used during the cleaning process.
- Contribute to achieving Lean Goals and continuous improvement processes.
- Other duties as assigned.

REQUIRED QUALIFICATIONS:

Education:

- Completion of secondary education is required.

Experience:

- Minimum of 2-3 years of experience in a pharmaceutical / GMP production environment.

Knowledge, Skills, Abilities:

- Demonstrated competencies in CPL’s core values.
- Flexible with the ability to adapt, respond quickly and manage change in a fast-paced environment.
- Computer proficiency, strong attention to detail including demonstrated reading and numeracy skills.

PHYSICAL DEMANDS/WORKING CONDITIONS:

- Confined space entry may be required.
- Heavy lifting may be required.
- Repetitive hip and upper body twisting movements.
- Visual acuity necessary.
- Mechanical aptitude and manual dexterity necessary

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.

Afternoon Shift

📌 Production Cleaner Technician (Mississauga)
🏢 Contract Pharmaceuticals
📍 Mississauga