Support GMP production leadership at Septodont’s Novocol Pharma site with documentation expertise and proactive problem solving. Coordinate teams and equipment in Cambridge, Ontario.

The Lead Hand III helps deliver pharmaceutical batches on time and right the first time. Reporting to the Production Supervisor, this position coordinates shift resources, provides timely updates, and escalates risks. It also drives operator coaching, corrective actions, SOP revisions, and cross-functional project support.

Key Responsibilities:

- Organize teams around schedules, milestones, resources, and production priorities
- Act as subject matter expert for equipment, products, and processes
- Review documentation for completeness, accuracy, and GDP compliance
- Drive corrective and preventative actions for documentation errors




- Represent Production on cross-functional project teams and audits

Requirements:

- High school completion or college certification, diploma, or studies
- Two years’ pharmaceutical manufacturing or related environment experience
- Leadership and interpersonal skills supporting interdepartmental collaboration
- Proven ability to lead, execute, solve problems, and achieve goals
- Proactive, independent approach with creative problem-solving ability

Apply production leadership, GDP documentation, GMP compliance, and cross-functional coordination skills as Septodont’s Lead Hand III.

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📌 GMP Production Shift Lead (Cambridge)
🏢 Septodont
📍 Cambridge