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Sterile Injectable Production Lead
Job Description & How to Apply Below
Guide sterile injectable cartridge production at Novocol Pharma, applying mechanical troubleshooting and GMP knowledge. Work in Cambridge, Ontario, supporting compounding and filling operations.
As Lead Hand III, you coordinate shift activities for Novocol Pharma’s sterile injectable manufacturing environment. You serve as an equipment, product, and process resource while organizing personnel, supplies, and production priorities. The position supports quality output, documentation compliance, training, and issue escalation.
Key Responsibilities:- Coordinate compounding or filling activities throughout the assigned shift
- Maintain component, operating supply, gown, and PPE availability
- Support new equipment and process introductions through training
- Inspect work areas and prevent cross-contamination risks
- Communicate priorities and issues with supervisors and other shifts
- High school completion, college certification, diploma, or ongoing completion
- Two years’ experience in pharmaceutical manufacturing or related environments
- Ability to work independently in high-pressure, varied conditions
- Strong written and verbal communication skills
- Flexibility to work occasionally outside normal hours
Use sterile manufacturing knowledge, production coordination, and troubleshooting ability to support compliant Novocol Pharma operations and product quality.
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