|Job Category||Office Admin & Legal|
|Application Deadline||May 31, 2020|
|Experience Required||3 years|
|Job Duration||1 year|
|Education Required||College Diploma|
Working as part of the Program Management Office, your responsibilities will include, but are not limited to:Manage Engineering Change Request documentation (DCP, DCO, etc.)Edit and manage project planning documents.Facilitate and document Design Reviews.Edit and process report type documents as required (e.g. Validations, Verifications, Engineering Files, etc)Research information in order to provide input to change requests and other documentation changes and system changes.Safeguard the environment and facilitate a safe and healthy workplace culture.Miscellaneous other duties as may be required.
To be considered for this position, you will have the following education, skills, and abilities:Post-secondary degree in Sciences or Arts3-5 years of related experience in Quality systems documentation.Ability to work independently and exercise judgment and initiative in dealing with a variety of duties and responsibilities.Ability to clearly, concisely and accurately convey communications.Ability to form and develop interpersonal, professional relationships; displays socially and professionally appropriate behavior.Ability to prioritize and handle multiple tasks.Ability to create GMP and GLP process documents in collaboration with subject matter experts.Ability to proactively address potential challenges created by changes in process documents.Ability to coordinate documentation which requires negotiation with multiple stakeholders.Basic knowledge of GMP, GLP and Quality Assurance requirements, and technical writing.Experience in quality report writing and corrective action preventative action an asset
If you are interested in this role, please contact
Only those who are qualified for the role will be contacted.