Facilities QA Associate

  • Category
    Industrial & manufacturing - Quality Control
  • Job type
  • Location
    Ottawa, Ontario

Adecco is currently hiring a full-time Facilities QA Associate for our Medical Manufacturing client in Ottawa West. This is a 1 year contract opportunity offering Full Time hours. The salary for this position will be determined based on education and experience.
As part of the Facilities Engineering team, the successful candidate will play in a key role overseeing quality adherence pertaining to Building, Facilities & Utilities Systems in a medical device manufacturing environment. Candidate will be considered the subject matter expert and use your knowledge to understand existing processes and implement continuous improvement initiatives. 
Facilities QA Associate Responsibilities:

  • Responsible for implementing and maintaining effectiveness of Quality System in Facilities;
  • Coordinate CAPA (corrective action, preventive action) system activities in a timely manner including effectiveness checks; these tasks include:
  • Generate (where required) and manage CAPA documents (ERs, PCs, CAs, PAs, Investigations);
  • Investigations into non-conformances (NCRs) and documentation of findings and Corrective Actions in Quality Reports (QRs);
  • Be the Initiator, Evaluator, Resolution Planner, Investigator to complete CAPA documents;
  • Support facilities and provide guidance on how to document and manage CAPA activities;
  • Prepare and present quality metrics on a daily, weekly and monthly basis;
  • Support and lead Quality improvement initiatives and lead cross functional quality projects;
  • Complete Design Change, Validation, Verification and Document Change processes and approvals;
  • Identify and evaluate ways to improve the organization (cost reductions, use of resources; policies/procedures, products); generating useful new ideas, approaches or techniques;
  • Ensure Quality System is maintained by updating and improving quality documents;
  • Identification, development and implementation of process improvement initiatives;
  • Develop change control packages to ensure facilities remain in qualified, validated state, including definition of appropriate requirements in change control documents, and tracking to completion the identified actions.
  • Facilities QA Associate Qualifications:

  • Bachelor’s Degree (Science, Engineering or related discipline);
  • 5+ years of related experience (such as Quality, Compliance, Engineering) within a regulated environment;
  • Knowledge of ISO 13485;
  • Knowledge of quality management techniques and the application and principles of quality engineering, strong knowledge and application of concepts, practices and procedures;
  • Experience with various quality system processes;
  • Experience in the Medical device, diagnostics or pharmaceutical industries is preferred;
  • Previous experience with regulatory agencies is preferred.
  • To be considered for this Facilities QA Associate opportunity in Ottawa West, please Apply Now!



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    Reference number CA_EN_1_021956_1355830

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