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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:

100 LifeSciences Parkway  Steinbach, MB R5G 1Z7

Fax: (204) 346-9388  Email: hrsteinbach@biovail.com

www.biovail.com

Biovail is an equal opportunity employer.

Only those selected for an interview will be contacted.

You may apply for this position online. Please complete all fields in the application form below. Be sure to attach your resume in the area provided. When you have completed the form, click 'Submit.'
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