CANADIAN BLOOD SERVICES Senior Quality Engineer (Quality Management System Designer) Full Time in Halifax, NS

Overview

CANADIAN BLOOD SERVICES

Branch Halifax NS CA

Position:
Senior Quality Engineer (Quality Management System Designer)
Location:
Halifax, NS

Ten years of experience within a manufacturing (Pharmaceutical, Medical Device, Biologics or related) environment with at least 5 years of quality process…

Senior Quality Engineer ( Quality Management System Designer )

Locations throughout Canada

Are you forward thinking and drive for creative solutions? Can you inspire others towards developing quality processes and systems? Do you have the ability to interact with various levels of stakeholders?

The Challenge:
Canadian Blood Services is built on passion and holds a unique position in the health care industry as a biologics manufacturer committed to delivering a growing range of world class products and services to Canadians. We need someone like you as a core member of the senior Quality Team, using your sound business acumen to analyze and develop key process indicators to monitor the Quality Management System performance and implement quality process improvements.

If you are excited about working with a team of dedicated quality professionals to deliver results at an enterprise level; are energized by complex business transformation challenges; and want to work for an organization where you are challenged and recognized, then we want to talk with you!

Responsibilities:
Develops and matures the Quality Management System and processes.

Designs the corporate Quality Management System to meet Canadian Blood Services (CBS) needs and confirms its fitness for purpose.

Identifies and recommends process and procedural changes based on regulatory requirements or business standards.

Works with technical experts, across the business, toward continuous improvement in system design, process flow and procedures, taking into account unique environments, situations etc.

Simulates and tests processes before go-live to ensure processes are performing as expected.

Identifies gaps and develops solutions on sub-optimal quality management system process performance.

Drives accountability for optimization of the corporate quality management system through system design update and standardization of the procedures.

Required Skills

University Degree in Engineering or Life Sciences or in a relevant discipline from a recognized academic institution.

Training in Quality Management System (ISO or others) will be an asset.

Ten years of experience within a manufacturing (Pharmaceutical, Medical Device, Biologics or related) environment with at least 5 years of quality process management, design and/or development.

Ability to assess maturity levels at both the system and process management levels.

Experience in workflow process modelling and process improvement methodologies.

Proven expertise in process analysis and design.

Excellent organizational, communication (written and verbal) and interpersonal skills.

Ability to work in a challenging and fast-paced environment and ability to be patient with ambiguity.

Proven project management skills.

Experience auditing Quality Management System is an asset.

Apply Here