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Quality Assurance Associate

En personne
Temps plein
Expérimenté

BIOVECTRA Inc. has an opening for Quality Document Control Associate. This is a permanent full-time position located in Windsor, NS.

The candidate will be responsible for:

  • Supporting the MasterControl Document Management System (Document control, Document Formatting, etc).
  • Servicing the document control email mailboxes by responding to user queries in a timely manner.
  • Issuance and archival of Production Batch Records.
  • Creation and issuance of Product Labels.
  • 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.

The successful candidate for this position should have:

  • 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 a food or drug manufacturing company is an asset.
  • Strong written and oral communications skills are necessary, as this position requires interaction with various levels of management, as well as interaction with external technical support teams.
  • Candidate must be able to handle a variety of tasks simultaneously and must be able to prioritize work to meet deadlines.
  • Candidate must be prepared to travel between NS and PE sites on a frequent basis for training and support.
  • Candidate must be available to support on weekends or evenings, if required.

BIOVECTRA offers a competitive salary and benefit package. Interested candidates are asked to apply by choosing the "Apply Now" button

Closing Date: October 3, 2024

Numéro de concours: 6744
Site Web d'entreprise: http://www.biovectra.com/

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À propos BioVectra Inc.

À propos BioVectra Inc.

BioVectra is a contract development and manufacturing organization (CDMO) that serves pharmaceutical and biotech companies with full-service cGMP outsourcing solutions for intermediates and active pharmaceutical ingredients (APIs). With over 45 years of experience, we are a reliable and innovative partner, specializing in:

  • Microbial Fermentation
  • Complex Chemistry
  • High Potency APIs
  • Biologics
  • Process & Analytical Development
  • Drug Development
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