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Quality Assurance Reviewer Reporting to the Quality
Assurance Supervisor, you will be responsible for reviewing and approving all
raw materials, in-process products, including manufacturing and packaging
records as well as investigations associated with Incident Reports and Deviation
Notifications. You will participate in the daily maintenance of inventory
status, QA system controls and tracking databases. In your role as QA Reviewer
you will work with various departments within the facility on a daily basis. You
will assist with the maintenance of product trending reports and provide support
to the QA Compliance Group in investigations, internal audits, and annual
product reviews. Shift work will be required. The successful candidate
will have a BSc or a College Diploma in chemistry or related science, a minimum
of two years experience in a pharmaceutical manufacturing environment including
QA/QC procedures and knowledge of FDA and TPP cGMP regulations. Excellent
written and verbal communication skills are required. A working knowledge
of computer software programs, specifically MS Office applications is an
asset. If you are interested in
this exciting opportunity please submit a resume, specifying this role to:
Fax:
(204) 346-9388
Email: hrsteinbach@biovail.com Biovail is an equal
opportunity employer. Only those selected for
an interview will be contacted.
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