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Specialist Quality Document Intermediate
12 month contract

 
Positions are need to be filled ASAP. 

Location: Ottawa

CLOSING DATE: APRIL 30, 2020

Our client is a worldwide leader in fundamentally changing healthcare delivery at the point of care with solutions that are intuitive, innovative, reliable, and cost-effective for our customers. 

JOB DESCRIPTION:

Our client is currently seeking a Quality Document Specialist (Intermediate) for their Ottawa test cartridge manufacturing facility. The main responsibility in this role will be to maintain ongoing daily CAPA departmental activities, and provide assistance for Exception Report documentation to other areas of the company, as needed.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Coordinate meetings with other departments to ensure timely execution of Exception Reports.
  • Support CAPA investigation documentation activities with input from investigation owners.
  • Provide guidance and coaching for CAPA Owners and Investigation Owners.
  • Participate and support internal and external inspections and assist with implementing solutions to audit findings.
  • Track and trend CAPA metric data and create presentations for management reviews
  • Other tasks and duties as may be assigned.

EDUCATION:

An Undergraduate University Degree in Engineering, Science, or related discipline preferred, or equivalent experience.

SKILLS, KNOWLEDGE AND ABILITIES:

  • 1-5 years working experience in a related field.
  • Working knowledge of CAPA procedures
  • Ability or aptitude to work on complex problems/issues.
  • Demonstrated initiative and problem-solving skills; critical thinking skills.
  • Good analytical, communication and interpersonal skills.
  • Good development and technical writing skills.

Send Resume to:

Charlotte Quesnel: c.quesnel@maxsys.ca

 
 
 

COMPANY WEBSITE

Intermediate Engineer
Building/Facilities/Utilities Systems Quality Specialist

 
Positions are need to be filled ASAP. 

Location: Ottawa

CLOSING DATE: APRIL 30, 2020

Our client is a worldwide leader in fundamentally changing healthcare delivery at the point of care with solutions that are intuitive, innovative, reliable, and cost-effective for our customers. 

JOB DESCRIPTION:

As a member of the Facilities Department, you will play in a key role overseeing quality adherence pertaining to Building, Facilities & Utilities Systems in a medical device manufacturing environment.   You will be considered the subject matter expert and use your knowledge to understand existing processes and implement continuous improvement initiatives. 

  • 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
  • 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.
  • 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.

EXPERIENCE

  • Typically requires 2+ years of related experience (such as Quality, Compliance, and Engineering) within a regulated environment.
  • Experience with various quality system processes
  • Experience in the Medical device, diagnostics or pharmaceutical industries is preferred.
  • Previous experience with regulatory agencies is preferred.

KNOWLEDGE, SKILLS AND ABILITIES

  • Bachelor’s Degree in STEM, or equivalent;
  • 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.
  • Ability to influence and lead without direct authority;
  • Ability to collaborate effectively with multidisciplinary team members and also to work independently;
  • Experience in the development, validation, or quality review of high volume automation is an asset.
  • Experience with statistical software an asset.

Send Resume to:

Charlotte Quesnel: c.quesnel@maxsys.ca

 
 
 
 

COMPANY WEBSITE

Intermediate Quality Assurance Specialist

 

Working with designers, developers and product managers in an agile development environment to create new products and support WorldReach’s existing products.

Responsibilities:

  • Design, write, and execute various types of tests for regression, performance, load and functional acceptance tests both manual and automated with input from development and business analysts as required; validate the results.
  • Analyze, assess and create test scenarios and test cases. Monitor and validate results.
  • Assist in the development and maintenance of automated regression testing environment.
  • Contribute testing knowledge to aid in the definition of acceptance criteria during the requirements gathering process for waterfall projects and during sprint planning and review for agile projects
  • Work with development to ensure interoperability with third party products, operating systems, and existing software for testing.
  • Ensure issues found are properly tracked throughout the software lifecycle, from discovery to closure.
  • Assist in process improvement initiatives related to software testing.
 

MORE INFORMATION & APPLICATION - CLICK HERE!

Quality Manager

Location: Kingston, ON.

Key Responsibilities: The Quality Manager is responsible for ensuring that Quality System requirements are effectively established and maintained, and for reporting on the performance of the Quality System to management.  The Quality Manager manages compliance activities pertaining to Food and Drug Administration (FDA) Quality System Regulation, ISO Quality System standards, and other international harmonized standards/guidelines. 

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General Manager North American Training

Full-time.

Location: Guelph, ON.

Key Responsibilities: The Registrar Company, Inc. (TRC) in Guelph are looking for an individual with some significant experience in the training business to work with them to create and grow a new business.

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Manager, Quality Systems

Full-Time, Permanent Position.

Location: OMS Algoma - Ottawa, ON.

Key Responsibilities: Provide leadership and guidance to the Home Care operations teams in integrating quality, safety, and risk management practices within the workplace culture of the division. Responsible for the overall quality management system within the Home Care division. This position will manage a team of 3 associates. Only select applicants will be contacted regarding the position.

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