TorontoFull TimeEngineering
Remotely
exceldocumentationms officecapagmpinternal auditschange controliso 17025
Job Description
📋 Description
- Review and determine status of quality documents (raw lab data, validation studies, logbooks
- Support maintaining Quality System; draft/update quality procedures
- Assist internal and external audits
- Ensure reports and raw data comply with GMP and ISO 17025; accurate per study protocol and SOPs
- Interact with staff to obtain information for reports and present deficiencies/improvements
- Log and review complaints; compile ISO 17025/GMP documents for evaluation
🎯 Requirements
- Knowledge of ISO 17025 and GMP requirements
- GMP experience is an asset
- Fluent English both written and spoken
- Excellent communication, organizational skills, attention to detail
- Ability to work independently and in a team; multitask and stay calm under pressure
- Professional demeanor; maintain discretion for confidential matters
🎁 Benefits
- Health & dental, life and disability insurance
- RRSP with 3% company match, paid holidays, paid time off
- Relocation: relocation to Mississauga, ON expected in 2026
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