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Added 41 mins ago
AA
Spécialiste en ingénierie de la sécurité des commandes de vol/Flight Controls Safety Engineering Specialist
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- Full-time
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Cencora

Quality Assurance Release Specialist

ON, Canada
Milton, ON, Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Oct 21, 2026

Original job description

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Job Details

This role is in support of Cencora’s patient and provider support and pharma commercialization services in Canada marketed through our Innomar Strategies business.

This job profile description is a standardized, non-contractual reference description and global reference tool provided for organizational consistency and talent architecture purposes across Cencora. It does not alter actual job duties, responsibilities, reporting lines, working conditions, grading, compensation, or other essential terms and conditions of employment.

Actual duties and responsibilities may vary based on business needs, local requirements, and operational practices. Where a team member's role is governed by an employment agreement, local terms and conditions, prior job description or collective bargaining agreement, those documents shall prevail in case of any inconsistency. Mandatory local laws shall also prevail.

Monitors adherence to QMS requirements and applicable good practices across assigned operational activities and programs.
Maintains controlled documents and quality records, including SOPs, work instructions, forms, templates, and retention logs.
Tracks deviations, complaints, and CAPAs through closure, including documented investigations, corrective actions, and effectiveness checks.
Prepares audit and inspection materials, compiles objective evidence, and tracks response actions to completion.
Generates routine quality metrics and prepares quality reports that identify trends, recurring issues, and improvement opportunities.
Delivers assigned quality training and maintains training matrices and compliance reporting for assigned populations.
Assists with supplier and subcontractor qualification activities and maintains documentation for ongoing supplier quality oversight.

Education:

Bachelor's degree in life sciences, business administration, supply chain, or a related field, or equivalent experience required.

Work Experience:

Less than 2 years of experience in quality assurance/quality management within a regulated and/or operational services environment (e.g., GxP/GDP, logistics/distribution, shared services, customer contact centers, or technology delivery), or a related field required.

Certifications:

Certified ASQ Certified Quality Auditor (CQA), Certified Professional in Healthcare Quality (CPHQ), ISO 9001 Lead Auditor (QMS), or equivalent preferred. Certified Lean Six Sigma Green Belt or Black Belt preferred. Certified ISTQB Certified Tester – Foundation Level (CTFL) or equivalent preferred.

Skills & Knowledge:

Knowledge in quality management system (QMS) concepts and documentation control.
Knowledge in applicable good practices and regulated-quality principles (e.g., GxP/GVP/GDP) and audit expectations.
Knowledge in CAPA fundamentals, including deviation/complaint handling, root cause methods, and effectiveness checks.
Knowledge in internal and external audit/inspection readiness practices and evidence requirements.
Knowledge in risk management and change control principles within a quality environment.
Knowledge in supplier/subcontractor quality oversight concepts and qualification documentation.
Knowledge in quality metrics and trend analysis concepts for continuous improvement.
Knowledge in data integrity and good documentation practices.
Ability to interpret and apply procedures, work instructions, and quality standards to operational scenarios.
Ability to document quality events and investigations with clear, complete, and traceable records.
Ability to organize and maintain training matrices, training records, and compliance reporting.
Ability to analyze quality data, identify trends, and communicate findings through standard reports.
Ability to prepare audit documentation packages and track actions to closure.
Ability to use common business applications and quality platforms (e.g., eQMS, document management systems) to manage records and workflows.

What Cencora offers

We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members’ ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.

Full time

Equal Employment Opportunity

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned

Accessibility Policy

Cencora is committed to fair and accessible employment practices. When requested, Cencora will accommodate people with disabilities during the recruitment, assessment and hiring processes and during employment.

This posting is intended to fill an existing vacancy for our Quality Assurance Release Specialist role.

Affiliated Companies:

Affiliated Companies: Innomar Strategies

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More about this job

Responsibilities

The Quality Assurance Release Specialist monitors adherence to QMS requirements and maintains controlled documents and quality records. They also track deviations, complaints, and CAPAs while preparing audit materials and generating quality metrics.

Requirements

Candidates must have a bachelor's degree in life sciences, business, or a related field. Less than 2 years of experience in quality assurance within a regulated environment is required.

Skills

Quality management system
Document control
GxP
GDP
CAPA
Deviation handling
Complaint handling
Root cause analysis
Audit readiness
Inspection readiness
Risk management
Change control
Supplier quality oversight
Quality metrics
Data integrity
Good documentation practices

Benefits

Medical care
Dental care
Vision care
Backup dependent care
Adoption assistance
Infertility coverage
Family building support
Behavioral health solutions
Paid parental leave
Paid caregiver leave
Training programs
Professional development resources
Mentorship programs

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
QMS
GxP
GDP
GVP
CAPA
SOP
Audit
Inspection
Root Cause Analysis
Risk Management
Change Control
Data Integrity
Good Documentation Practices
ASQ
CQA
CPHQ
ISO 9001
Lean Six Sigma
ISTQB
CTFL
eQMS
Document Management Systems
Compliance
Regulatory
Operational Services
Pharma Commercialization
Innomar Strategies
Cencora

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