Scientist II Jr Scientific Technical Writer

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting
**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:**
Assist with preparation of analytical method validation protocols and reports, method transfer protocols and reports, analytical methods, and specifications used by the Development Laboratory ensuring they meet current regulatory, corporate and industry standards.
Perform bench work to support client projects.
**Shift schedule:**
Monday u2013 Friday 9 AM u2013 5:30 PM
**Day in the Life:**
Independently carryout LC/MS, HPLC, dissolution and physicaltesting analysisfollowing established ...