Compounder
- Mississauga, ON, Canada
$50,000 to $55,000 CAD / year · Contract
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Job details
- Pay
- $50,000 to $55,000 CAD / year
- Job type
- Contract
- Apply by
- Posting language
- English
- Posted
Original job description
Job Type
12-Month Contract (Current Vacancy)
Afternoon Shift - 1 position
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 and wellness program.
Job Summary
To manufacture products in accordance with the Manufacturing Work Orders. Ensure product quality by following the relevant Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs) as well as products are made to efficiency standards.
Job Responsibilities
REQUIRED QUALIFICATIONS:
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
12-Month Contract (Current Vacancy)
Afternoon Shift - 1 position
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 and wellness program.
Job Summary
To manufacture products in accordance with the Manufacturing Work Orders. Ensure product quality by following the relevant Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs) as well as products are made to efficiency standards.
Job Responsibilities
- Responsible for working in compliance with established safe work practices and procedures; properly uses personal protection and safety equipment as required by CPL; reports any injury or illness immediately and notifies CPL of any hazards, unsafe acts or conditions in the workplace.
- Responsible for correctly filling out all applicable manufacturing tags and documents accurately adhering to GDPs, GMPs and SOPs.
- Exercises “Right First Time” documentation practices on all documentation.
- Perform cleaning, sanitation and re-sanitation of manufacturing product-contact equipment, utensils and premises as per approved SOP to ensure GMP compliance. This includes disassemble, reassemble and storage of manufacturing equipment as per standard operating procedures.
- Weigh, verify and compound raw materials, performing set up and manufacturing of batches as per Manufacturing Work Order (MWO), while strictly adhering to GMPs, SOPs and labour standards
- Continue to acquire the necessary knowledge needed for all manufacturing activities and participate in continuous improvement initiatives
- Responsible for proper assembly, set up and use of equipment.
- Perform cleaning by entering Confined Space in compliance with Safety procedures and guidelines.
- Ensure that equipment and suites in the Manufacturing area are maintained in accordance with GMPs and SOPs.
- Checks meters, scales, load cells, temperature indicators, mix indicators and other manufacturing equipment for proper calibration/accuracy before use.
- Contribute to achieving Lean Goals and continuous improvement.
- Other duties as assigned
REQUIRED QUALIFICATIONS:
- Minimum post secondary education is required in a related field. Equivalent experience will also be considered.
- Minimum of one to two years of team based high volume pharmaceutical or regulated manufacturing experiences.
- Good English verbal and written communication skills.
- Flexible with the ability to adapt, respond quickly and manage change in a fast-paced environment.
- Ability to work under given timelines, multi-task and attention to detail with a high degree of accuracy
- Attention to detail, thoroughness, strong mechanical aptitude and proven technical competency is highly desirable.
- Demonstrate competencies in CPL’s core values Excellence, Rigor, Ownership, Integrity and Agility.
- May be required to manually handle heavy cases and drums of materials on and off skids without mechanical assistance.
- Push and pull automatic hand truck.
- Pulling, pushing, and pumping with manual pump truck, heavy skids.
- Confined space entry may be required.
- A properly fitted respirator must be worn in Manufacturing rooms.
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
More about this job
Responsibilities
Weigh, verify, and compound raw materials and manufacture batches according to work orders, while following GMPs, SOPs, safety procedures, and efficiency standards. Clean and maintain manufacturing equipment and areas, complete accurate production documentation, verify equipment calibration, and contribute to continuous improvement.
Requirements
A minimum of post-secondary education in a related field is required, although equivalent experience may be considered. Applicants need one to two years of team-based experience in high-volume pharmaceutical or regulated manufacturing, along with strong English communication, adaptability, accuracy, and mechanical aptitude.
Skills
- Pharmaceutical Compounding
- Batch Manufacturing
- Raw Material Weighing
- Good Manufacturing Practices
- Standard Operating Procedures
- Good Documentation Practices
- Equipment Setup and Operation
- Equipment Cleaning and Sanitation
- Quality Control
- Calibration and Accuracy Checks
- Safety Compliance
- Confined-Space Work
- Documentation Accuracy
- Mechanical Aptitude
- Attention to Detail
- Continuous Improvement
Benefits
- Paid Time Off
- Employee Assistance Program
- Work-Life Balance
- Employee Recognition Program
- On-Site Parking
- Discounted Gym Membership
- Wellness Program
- Deferred Profit-Sharing Plan
Visa sponsorship
Not detected in the job text
Categories
- Manufacturing
- Science & Research
- Security & Safety
Keywords
- Pharmaceutical Manufacturing
- Contract Manufacturing
- Pharmaceutical Compounding
- Manufacturing Work Order
- Batch Manufacturing
- Raw Materials
- Good Manufacturing Practices
- Standard Operating Procedures
- Good Documentation Practices
- Right First Time Documentation
- Quality Compliance
- Equipment Setup
- Equipment Assembly
- Equipment Cleaning
- Sanitation
- Re-Sanitation
- Confined-Space Entry
- Personal Protective Equipment
- Respirator
- Calibration
- Scales
- Load Cells
- Temperature Indicators
- Mix Indicators
- Lean Goals
- Continuous Improvement
- Regulated Manufacturing
- Safety Procedures
- Afternoon Shift
- 12-Month Contract