Process Engineering II
Location
Mississauga, ON
Job Type
Full-time
Category
other-general
Posted
June 18, 2026
**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 (https://www.patheon.com/us/en/our-capabilities/small-molecule/oral-solid-dose.html) to commercial supply (https://www.patheon.com/us/en/our-capabilities/small-molecule/oral-solid-dose.html) in 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...
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 (https://www.patheon.com/us/en/our-capabilities/small-molecule/oral-solid-dose.html) to commercial supply (https://www.patheon.com/us/en/our-capabilities/small-molecule/oral-solid-dose.html) in 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...