Employment 

Temporary Pilot Manufacturing Facility Operator - Ref # PS-1117

July 29, 2010

QLT Inc.

1. Follows Standard Operating Procedures (SOPs) and complies with cGMP and safety regulations for the production of clinical and development drug products.
2. Writes, updates, and maintains SOPs.
3. Operates and conducts basic troubleshooting of production equipment.< /LI>
4. Performs in-process and final product inspection of components and finished product.
5. Maintains complete and accurate records including equipment logs and investigation reports.
6. Completes batch records and complies with safety regulations and cGMPs.
7. Maintains inventory and assists with cycle counts and work orders.
8. Maintains housekeeping of PMF and equipment.
9. Collaborates and interacts with others in a mutually supportive and co-operative manner that reinforces the concept that staff at all levels are expected to seek ways in which they can support and assist others to achieve expected results, as well as to be effective in their own accountability areas.

1. Technology diploma or Life Science degree with up to one year of related experience, preferably in a clean room environment or an equivalent combination of education and relevant work experience.
2. Working knowledge of manufacturing and aseptic techniques, an understanding of process development, and a proven GLP / GMP standard is preferred.
3. Knowledge of Microsoft Office products, specifically Word and Excel.
4. Good oral and written English communications skills.
5. Proven team player, and motivator.
6. Excellent attention to detail.
7. Ability to lift up to 50 lbs and work extended hours while standing.
8. Ability to work flexible working hours with the possibility of future shift pattern hours.
9. As required by Canadian and pharmaceutical regulations and Good Manufacturing practices, anyone engaged in the manufacture and packaging of pharmaceutical products must complete annual medical examinations to confirm that they are in good health and free from communicable conditions. In addition, employees who are involved in visual inspection of the pharmaceutical products must also complete annual eye examinations to assess that they have good vision (with or without correction) and are not color blind.