Temporary Process Specialist 1 - Ref # PS-1116
July 29, 2010
QLT Inc.
QLT Inc. is a biotechnology company dedicated to the development and commercialization of innovative therapies for the eye. We are focused on our commercial product Visudyne® for the treatment of wet-AMD, developing drugs to be delivered in our proprietary punctal plug delivery system, as well as developing our synthetic retinoid program for the treatment of certain inherited retinal diseases. For more information, visit our website at www.qltinc.com.
DESCRIPTION
Under supervision and guidance, responsible for conducting clearly defined experiments which involve the development of processes and technologies for the manufacture of pharmaceutical products.
SPECIFIC ACCOUNTABILITIES
- Applies knowledge of development methodologies, techniques, processes and procedures in conducting clearly defined experiments.
- Under supervision and guidance, develops and performs a variety of elaborate and multi-step tests, determinations, analytical procedures, and investigations using both standard and special procedures, and equipment examinations.
- Makes detailed observations, maintains records, describes methods, prepares data, analyzes and summarizes results. Reviews experimental process and data with the Supervisor, and/or coworkers as appropriate.< /LI>
- Explains reasons for variances and may interpret results and make recommendations on findings. Prepares written reports and analysis of experiments.
- Uses designated computer programs to analyze data and develop graphic or tabular representation of results.
- Communicates results and analysis to working group.
- Suggests variations and/or modifications to standard procedures and methods.
- Writes operating procedures for developed methodology.
- Demonstrates equipment, techniques and procedures and standards to lab personnel.
- Develops awareness of literature related to specialized area of research.
- Prepares reagents, solutions and culture media as required. Maintains the lab and perform cleaning sterilization and other routine duties to keep laboratory neat, clean and in operational order.
- Conducts all activities in accordance with scientific standards, OH&S regulations, and established policies and practices.
- May participate in manufacturing processes in the PMF as well as routine procedures for PMF upkeep including changing of gowns, stocking daily supplies, and performing daily cleaning procedures.
- 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.
- Bachelor degree in Biological, Physical or Pharmaceutical Sciences and up to one year of related experience.
- Good oral and written communication skills.
- Good critical thinking and decision making skills.
- Proficient with Microsoft Office products, specifically Word, Excel, and Microsoft Project.
- Knowledgeable in general laboratory Occupational Health and Safety procedures.
- Topical, injectable and/or device process development experience an asset.
- Experience with hydrophobic drugs an asset.
How To Apply:
Apply online at www.qltinc.com - Ref # PS-1116
