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Baxter
Quality Associate-II, QA AssuranceBaxter • Alliston, Ontario, Canada
Quality Associate-II, QA Assurance

Quality Associate-II, QA Assurance

Baxter • Alliston, Ontario, Canada
30+ days ago
Salary
CA$86,400.00 yearly
Job type
  • Full-time
Job description

This is whereyour work makes a difference.

At Baxter we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today tomorrow and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together our community is driven by a culture of courage trust and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations and we hold each other accountable for delivering exceptional results.

Here you will find more than just a jobyou will find purpose and pride.

Your Team at Baxter

Within Quality every role matters. Baxters products are shipped worldwide to patients in need. Whether you build new processes or solve unique production challenges you have the trust and chance to bring creativity. No matter your role your work will impact part of our global operation.

The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds we will always choose quality. Our patients come first always.

The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves so does the way our team approaches work as it strives to build top-of-the-line products.

We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable ethical and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when theres a new insight or opportunity to improve something. This open dialog builds trust within the team and helps develop a better product for our customers.

What youll be doing

  • Provide front line day-to-day assistance on product quality issues to ensure GMP regulatory and procedural compliance to maintain high standards of quality.
  • Support during assigned Shift with the requirement to support plant overtime and planned shutdowns when applicable.
  • Provide technical assistance on review and approval of department-related procedural changes product quality concerns reinspections new product introductions and protocols.
  • Support timely follow-up on quality exceptions and their preventative/corrective actions.
  • Support initiation/investigation and approvals of non-conformance events in the Trackwise system.
  • Act as SME for Electronic Batch Record (EBR) and SPC or equivalent experience.
  • Perform change control assessments/executions and approvals.
  • Ensure control of defective WIP materials (quarantine retention and disposal areas) to keep segregation movement documentation and timely follow-up within the plant in sync with regulatory and compliance requirements.

What youll bring

Required:

  • University Degree or equivalent experience Bachelor of Science or equivalent experience.
  • 1 3 years experience in manufacturing and quality roles.
  • Prior experience working in a GMP setting.
  • Knowledge of cGMP ISO and regulatory standards.
  • Diligent with the ability to work effectively under pressure.
  • Strong written and verbal communication abilities negotiation capabilities and the capacity to collaborate with individuals at every level of the organization.
  • Ability to build positive relationships and partner with internal and external collaborators.
  • Strong ability to balance multiple priorities.
  • Strong analytical and problem-solving skills with critical thinking abilities.
  • Intermediate to Advanced proficiency in MS Office Suite.

Preferred:

  • 3 years with exposure to various areas of the manufacturing environment.
  • Experience in pharmaceutical healthcare or food manufacturing environments.
  • Experience with continuous improvement methodologies Lean 6S Kaizen TPM DMAIC.

Join us in our mission to make a global impact with your outstanding skills and dedication to quality!

Garbing Processes

We understand that compensation is an important factor as you consider the next step in your career. At Baxterwe are committed to equitable pay for all employees and we strive to be more transparent with our pay practices. The estimated salary range for this position is $86400 - $129600 annually which reflects base salary as wellas estimated target payout under the Management Incentive Compensation Plan. Individual pay will bedetermined based upon skills expertise and experience and the incentive which is contingent upon company andindividual performance outcomes. For questions about this our pay philosophy and available benefits please speak to the recruiter if you decide to apply and are selected for an interview.

This posting is for a current existing vacancy within our organization. We are actively seeking qualified candidatesto fill this open position. If you are interviewed for this position we will advise you within 45 days of the interview
as to whether or not you were successful in obtaining the position. Information submitted as part of the jobapplication process will be kept on file for 3 years from the date of submission in accordance with legislative
requirements.

As part of our recruitment process Baxter Corporation may use AI tools to assist screening candidates and assistin evaluating candidate qualifications. All final hiring decisions are made by the hiring manager and recruitmentteam

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race color religion gender national origin age sexual orientation gender identity or expression protected veteran status disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If because of a medical condition or disability you need a reasonable accommodation for any part of the application or interview process please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams where fraudulent parties pose as Baxter employees recruiters or other agents and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself review our Recruitment Fraud Notice.


Required Experience:

IC


Employment Type : Full-Time
Experience: years
Vacancy: 1
Yearly Salary Salary: 86400 - 129600
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Quality Associate-II, QA Assurance • Alliston, Ontario, Canada

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