**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
**Division/Site Specific Information:**
Our Mississauga facility covers all phases of drug product development from early-phase formulation development to clinical trial material ( commercial supply ( the same plant using scalable equipment for non-GMP and GMP work.
**Discover Impactful Work:**
Support the Technical Operations department in generation of protocols, master batch record review, batch analysis, Quality Investigation Report/Quality Deviation Report (QIR/QDR) follow-up, process execution and equipment procurement.
**Day in the Life:**
Technology transfer. Responsible for transfers and launches to the site. Includes process scale-up and process optimization.
Inves...