**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

**Job Description**

**Site Specific Information**

Our Whitby Site specializes in commercial manufacturing (https://www.patheon.com/us/en/our-capabilities/small-molecule/oral-solid-dose.html) for a full range of conventional dosage forms (https://www.patheon.com/us/en/our-capabilities/small-molecule/oral-solid-dose.html) with specialized capabilities, and houses a fully integrated pharmaceutical development services (PDS) facility.

**Discover Impactful work:**

To conduct internal, external and client Good Manufacturing Practices (GMP) audits.

**Day in the Life:**

+ Performinternal Good Manufacturing Practices audits of all departments asrequiredand prepare writtenreportsto document the findings.

+ Participate in thesite Fit and Finish Audit.
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