Quality Document Control Associate - Charlottetown, Canada - BioVectra Inc.

BioVectra Inc.

Verified Company

Charlottetown, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

BIOVECTRA Inc. has opening for
Quality Document Control Associate. This is a permanent, full-time position
located at either
Nova Scotia or PEI.

Supporting the MasterControl Document Management System (Document control, Document Formatting, etc).
Servicing the document control mailboxes by responding to user queries in a timely manner.
Issuance and archival of Production Batch Records.
Design, control and issuance of Product Labels.
Ability to travel between NS and PE sites on frequent basis for training and support.
Archival, retention and disposal of Quality Management Records.
Participating in the internal audit program and supporting external audit requirements.
Monitoring and enforcement of GMP requirements during day to day operations within the department.
Prioritizing and timely completion of tasks to meet and exceed Key Performance Indicators.
Timely escalation of problems and issues to their supervisor to prevent any delays and risk compliance.
Preparing or assisting in the preparation of data and reports for KPIs.
Participating in document lifecycle activities of SOPs, and QA review and approval of SOP changes.
Adhering to BIOVECTRA's Health and Safety Policy as outlined in CP0010 Occupational Health and Safety Policy, Statements of Principle, and Responsibilities.
Additional duties assigned, based on business needs and the department supervisor's request.
Post-Secondary Education.
One year direct experience in a Quality Unit position.
Working knowledge of MS office tools such as Word, Excel, Outlook
Three years of work experience in a similar role in food or drug manufacturing company is an asset.