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Quality Control Supervisor/ Biological Assays for Validation to 85 K

Joan Edgar careers at sympatico.ca
Wed Jun 16 04:47:23 EST 2004

We are currently seeking an experienced Quality Control Leader or 
Supervisor with a minimum of 3 years experience in drug development, 
medical device, or related biotechnology sector. You will be initiating 
QC for the Orthobiologic/Tissue engineering development group, implement 
QC procedures and methods in developing the companies orthopedic devices 
for bone and cartilage engineering.

The duties also include: developing and adapting analytical and 
Biological assays for Validation.  This will include the drafting and 
technical writing of methods and validation procedures for all 
development applications on Clinical design paths. You will be 
responsible for adherence to Regulatory guidelines such as FDA TPP, 
including the required documentation.

You must have:  Thorough working knowledge of GLP/GMP, Validation of 
biological and analytical assays, and regulatory documentation
requirements as well as an MSc. or BSc. with related experience.
Location: Toronto

Please call Joan Edgar 416 222-1909 for more details.

J. Edgar and Associates Inc. . . partners in technical search serving
local and international networks.

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