Quality Assurance Associate - Brampton, Canada - Canadian Blood Services

Canadian Blood Services

Verified Company

Brampton, Canada

3 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Job category:
Quality and regulatory affairs

Job posting ID: 5587

Employment status:
Regular full-time

Position's anticipated start date:

Classification:
PTS/MGT/IT B

Salary/Rate of pay:
$77,500 - $91,000

Application deadline:

Application requirements:

Your uptodate resume.
We recommend you save a copy of the job posting for reference throughout the recruitment process.

Together, we can make all the difference in the lives of others.
Be part of a dynamic, collaborative and caring organization committed to saving and improving lives.

Thousands of patients depend on us every day for reliable access to safe blood, plasma, stem cells and organs and tissues.

If you are looking for a rewarding experience with a values and mission-driven team, join Canada's Lifeline and make a meaningful difference.

We acknowledge that the work of Canadian Blood Services spans many Territories and Treaty areas across the country, and we are grateful for the Traditional Knowledge Keepers and Elders who have guided us in this important work. We recognize the land and waters that have inspired our work and offer gratitude to those Indigenous peoples on whose territory we work, live and play._

About the role
Canadian Blood Services is looking for a
regular full-time Quality Assurance Associate to join our dynamic
Quality Assurance team.

The
Quality Assurance team is accountable for the systematic efforts taken to assure that all Canadian Blood Services' products and services delivered to the customer meets expectations of the customer.

Formula for success

Capitalizing on analytical skills, you will assist the organization in monitoring and continuously improving product and service quality. This involves collecting and analyzing data, facilitating root cause analysis, investigations, and overseeing the implementation of improvements.
Demonstrating flexibility and teamwork, you will utilize your ability to support the afterhours oncall team on a rotational basis. This showcases a commitment to teamwork and organizational responsiveness.
Maintaining connectivity and responsiveness, you will capitalize on your requirement to carry a cellular phone to support the afterhours oncall team. This ensures timely and effective communication during critical situations.
Adapting to diverse responsibilities, you will perform other duties as required. This showcases your adaptability and versatility to contribute effectively across various tasks and responsibilities within the organization.

Desired education and skills

Postsecondary level education in a relevant discipline from a recognized academic institution, or equivalent experience is required.
Certification in Quality Management Systems and/or certified Quality Engineer designation is required. Will consider an applicant currently working on certification, or an agreement to obtain certification.
Minimum of 10 years' experience within a manufacturing or pharmaceutical environment following Good Manufacturing Practices, with at least 5 years of Quality Management and Continuous Improvement experience.
Comprehensive knowledge of Quality Management System elements is required.
Comprehensive analytical, problemsolving and decision making skills are required.
Effective interpersonal skills along with proven ability to exercise sound judgment, tact and discretion, coach and facilitate discussions that promote the Quality Management System.
Demonstrated ability to think systemically and anticipate impact on people, systems and processes.

What we offer you

4 weeks' vacation
Annual performance award up to 6%
Comprehensive group health, dental and vision benefits for you and your family
Defined benefit pension plan
Employee discounts, wellness program, professional resources

What you can expect

This role will work in a hybrid environment with requirements to be onsite at one Canadian Blood Services production site within Canada 40% of the time/2 days of the week.
You will work Monday to Friday, 37.5 hours per week, 7.5 hours a day, additional hours may be required depending on project requirements.
If you are located outside of Ottawa, you may be expected to travel to our office location in Ottawa Alta Vista Rd, Ottawa, Ontario, quarterly for inperson team meetings when required.

Diversity and inclusion play a vital role in ensuring health equity for patients across Canada.

We are committed to reflecting Canada's population in our organization and fostering an environment where all employees can be their authentic selves, with equal opportunities to succeed and contribute.

We thank all applicants for their interest. However, only those considered for an interview or those invited to participate in an assessment will be contacted. Applicants who require accommodation should discuss their needs with us.