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Added 4 days ago
Senior Manager - Global Compliance Quality Assurance Review (5344)
TD
Toronto, ON
Full-time
The Senior Manager, Global Quality Assurance Review is responsible for leading risk-based quality assurance review activities across TD’s global Compliance program, with a primary focus on…
Added 1 month ago
Audit Manager II, Quality Assurance and Improvement Program- IT Audit (1094)
TD
Toronto, ON
Full-time
The Internal Audit Division Quality Assurance and Improvement Program (QAIP) team is responsible for the development and execution of the QAIP annual plan as well as evolving the QAIP…
Added 25 days ago
Senior Manager, Quality Assurance (Operations)
goeasy Ltd.
Mississauga, ON
Full-time
The Senior Manager, Quality Assurance will build and lead a tech-enabled QA program across Centralized Operations, using AI-enabled monitoring, speech and interaction analytics, dashboards,…
Added 9 days ago
Audit Manager II, Quality Assurance and Improvement Program- IT Audit (1094)
TD
Toronto, ON
Full-time
The Internal Audit Division Quality Assurance and Improvement Program (QAIP) team is responsible for the development and execution of the QAIP annual plan as well as evolving the QAIP…
Added 1 month ago
Senior Manager, Quality Assurance Automation
Walmart Canada
Mississauga, ON
Full-time
Position Summary...The role provides oversight for technology quality and delivery by guiding planning, testing, automation, and continuous improvement. The work may align platforms, teams,…
Added 2 months ago
Expert(e) senior, assurance qualité / Expert Senior, Quality Assurance
Bell Flight
Mirabel, Quebec
Full-time
Programme d’assurances collectives et soins de santé virtuels
Added 1 month ago
Senior Manager of Program Operations
Ontario Soil and Crop Improvement Association
Guelph, ON
Full-time
The Senior Manager of Program Operations is responsible for the effective operational management and delivery of agricultural and environmental programs administered by the organization.…
Added 3 months ago
Gestionnaire / Gestionnaire principal, Opérations qualité / Manager / Senior Manager, Quality Operations
Jubilant Pharma Limited
Montreal, Quebec
Full-time
…salaire de base hautement compétitif, des régimes complets d’assurance médicale, dentaire et d’invalidité, un régime de retraite collectif, ainsi que des programmes de santé et de…
Added 9 days ago
Responsable principal, Assurance qualité / Senior Manager, Quality Assurance
Jubilant HollisterStier CMO
Montreal, QC
Full-time
As Senior Manager, Quality Assurance, you will provide strategic and operational leadership for site Quality Systems and Quality Operations. You will ensure compliance with GMP/cGMP…
Added 2 months ago
Expert(e) senior, assurance qualité / Expert Senior, Quality Assurance
Textron
Mirabel, Quebec
Full-time
Programme d’assurances collectives et soins de santé virtuels
Added 12 days ago
Academic Quality Assurance Manager
McGill University
Montreal, QC · McLennan Library
Full-time
Reporting to the Director, Operations and Academic Programs within Teaching and Academic Programs, the Academic Quality Assurance Manager is responsible for managing and advancing…
Added 1 month ago
Gestionnaire Senior, Amélioration Continue MRO | Senior Manager, MRO Continuous Improvement
Pratt & Whitney
Longueuil, QC · Saint-Hubert, QC
Full-time
Titre du poste: Gestionnaire Senior, Amélioration Continue MRO
Added 1 month ago
Gestionnaire Senior, Amélioration Continue MRO | Senior Manager, MRO Continuous Improvement
RTX
Longueuil, QC
Full-time
Titre du poste: Gestionnaire Senior, Amélioration Continue MRO
Added 11 days ago
Manager - Quality Assurance
Marshall Land Systems
Moncton, NB
Full-time
Marshall Land Systems is seeking a Manager – Quality Assurance to join our team in Moncton, NB. Reporting to the Senior Quality Manager, the Manager – Quality Assurance will be responsible…
Added 4 months ago
Senior Program Manager – Sustaining Capital Project Alliance
Wood
Edmonton, AB
Full-time
Wood is seeking a Senior Program Manager to join our Canada Projects business in Edmonton, delivering some of the world's boldest and most critical projects. This opportunity is Hybrid.
Added 23 days ago
Quality Assurance Manager
Avmax Careers - Canada
Calgary, AB
Full-time
The Quality Assurance Manager reports directly to the Director of Quality.
Added 26 days ago
QNX Senior Quality Manager
BlackBerry QNX
Ottawa, ON
Full-time
We're looking for a Senior Quality Manager to play a pivotal role in auditing, maintaining, and advancing the quality, safety, and cybersecurity processes behind QNX software products. In…
Added 1 month ago
Quality Assurance Manager
Infrapipes
Huntsville, ON
$74,000 to $95,000 CAD / year
Full-time
We are currently seeking a Quality Assurance (QA) Manager to work out of our Huntsville, Ontario manufacturing location. This role will be responsible for managing the inspection and…
Added 26 days ago
QNX Senior Quality Manager
BlackBerry
Ottawa, ON
Full-time
We're looking for a Senior Quality Manager to play a pivotal role in auditing, maintaining, and advancing the quality, safety, and cybersecurity processes behind QNX software products. In…
Added 23 days ago
Gestionnaire principal(e) de programme – Solutions d'entreprise ERP / CRM / SAP | Senior Program Manager – Enterprise ERP / CRM / SAP
Pratt & Whitney
Longueuil, QC
Full-time
Titre du poste : Gestionnaire principal(e) de programme – Solutions d'entreprise ERP / CRM / SAP
Added 1 month ago
Gestionnaire principal(e) de programme – Solutions d'entreprise ERP / CRM / SAP | Senior Program Manager – Enterprise ERP / CRM / SAP
Pratt & Whitney
Mississauga, ON
Full-time
Titre du poste : Gestionnaire principal(e) de programme – Solutions d'entreprise ERP / CRM / SAP
Added 1 month ago
Gestionnaire principal(e) de programme – Solutions d'entreprise ERP / CRM / SAP | Senior Program Manager – Enterprise ERP / CRM / SAP
RTX
Mississauga, ON · Longueuil, QC
Full-time
Titre du poste : Gestionnaire principal(e) de programme – Solutions d'entreprise ERP / CRM / SAP
Added 3 months ago
Sr. Project Manager, Quality Assurance (QA)
Evonik
Burnaby, British Columbia
Full-time
…alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also…
Added 3 months ago
Sr. Project Manager, Quality Assurance (QA)
Evonik
Burnaby, British Columbia
Full-time
…alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also…
Added 10 days ago
Assurance Learning and Development Senior Manager
Pwc Canada
Toronto, ON
Full-time
Working across Program Management, Compliance and Operations, the Senior Manager creates clarity, drives continuous improvement, strengthens decision-making and helps position Assurance L&D…

Evonik

Sr. Project Manager, Quality Assurance (QA)

Burnaby, BC, Canada

Job type: Full-time
Experience: With over 25 years of experience and having transacted business in about 50 different countries,
Posting language: English
Posted: Jun 5, 2026

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Original job description

Note: This is an on-site role with the flexibility to work from home in accordance with Evonik's Smart Work Program.

Target Salary Range:

$101,500 – $135,300 per year (salary to be determined by education, experience, knowledge, skills and abilities of applicant, internal equity, and alignment with market data)

EVONIK Vancouver Laboratories (VAN), the operating drug delivery service site of Evonik Canada Inc., is a Contract Development and Manufacturing Organization (CDMO) that provides CMC services to biotechnology and pharmaceutical companies engaged in the development and manufacture of complex delivery-based drug formulations.

EVONIK has a successful track record of helping Customers move their programs forward. Evonik’s Vancouver business operations is a development partner to the world’s pharmaceutical companies for parenteral lipid nanoparticle drug products. As an enabling contract development manufacturing organization (CDMO) partner, we offer drug formulation design, process development, scale-up, and clinical production.

EVONIK’s range of services extends from initial formulation prototype identification, manufacturing process development & scale-up, analytical method development & validation to support raw material, in-process, release and stability testing, all the way through to sterile product manufacturing under GMP for Phase I-II clinical trials. Products include the LIPEX® line of Extruders, which are designed to enable small-scale to commercial scale manufacturing of liposomal drug products. With over 25 years of experience and having transacted business in about 50 different countries,

WHY EVONIK? Evonik offers an excellent Total Rewards Program including:

Competitive base compensation & bonus; employer paid health & dental benefits complimented with wellness education sessions; Financial planning resources & savings plans including RRSP & Defined Contribution pension plans; Generous vacation and paid time off to support Community Volunteer activities; Financial assistant for fitness memberships. And there is more...access to a Comprehensive Health Promotion program and Regional and Global resources for ongoing training and development. Best of all, you will work within a great team of professionals in an engaging workforce who value trust and openness. Are you looking to join a dynamic company with an exciting and expanding future in the pharmaceutical industry? Then Evonik is the next step in your career. Grow with us!

Click here to learn more from our Vancouver Laboratories employees:

https://www.youtube.com/watch?v=s5X15sKUEzs

WHY VANCOUVER?

Vancouver has something for everyone! British Columbia is beautiful and exciting. From the people, to the mountains, to the sprawling coastline, everywhere you look. Nestled on the warm Pacific Coast with the Rockies blocking cold arctic winds. Vancouver has the good fortune of being spared the typically chilly winters associated with Canada. Vancouver is often called ‘two cities in one’ because people are equally prone to enjoy the bustling nightlife and experiencing a plethora of activities in the surrounding nature. Imagine enjoying a day-long trek through our world-renowned rain forests, then heading into the city for a night out. Vancouver truly is as beautiful as people say and more.

What we offer

Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us.

Click on the link below to learn what our employees have to say about Evonik:

https ://careers.evonik.com/en/about/meet-the-team/

RESPONSIBILITIES

Maintain and revise QA related procedures, as needed.
Maintain cGMP training systems and perform on-site team member training in Quality related matters
Ensure GxP support and oversight, as applicable, for relevant site functions and activities
Support QA team members with Senior QA level knowledge, experience, guidance, coaching and mentoring, as required
Perform QA batch record review and disposition of manufactured early phase clinical product batches.
Provide final QA approval of investigations and disposition of any impacted product batches.
Evaluate deviations and propose batch rejections, if applicable.
Perform QA review and approval of the following, as needed:
Environmental monitoring data in GMP cleanrooms and adjacent areas, as well as Clean Utility monitoring data
Investigation of non-conforming product
Investigation of out of specification (OOS) results
Manage and approve Change Controls, as required for facilities, equipment, systems and processes, Corrective Action/Preventive Action (CAPAs), and Deviations
Provide direct or provide QA resources to support process development teams
Perform or support internal audits/self-inspections
Perform or support qualification of suppliers
Perform QA review and approval of the following:
Facility and equipment qualification protocols and final reports
Cleaning verification protocols
Analytical test method validation documentation
Provide or support QA review and approval of analytical methods, standards and specifications
Support, coordinate and/or host customer audits as required. Support audit responses creation and execution, as needed.
Effectively communicate with client QA personnel as project support
Provide QA support for development of validation strategies and validation plans, including Computer System Compliance (CSC) efforts.
Establish and manage QA tracking and trending of program measures and the preparation of periodic reports for management review. Maintain appropriate KPI´s to monitor performance and improvement.
Propose and develop continuous quality initiatives to improve efficiency and/or improve the level of control and compliance.
Support and promote the company safety program by obtaining and using all personal protective equipment as appropriate, observing all safety procedures and practices, and assuring that other employees similarly use personal protective equipment. Perform other duties as may be required by management.

REQUIREMENTS

Minimum B.S. degree in chemistry, biology, microbiology, biomedical or chemical engineering or equivalent education.
Preferably ten (10) to twelve (12) years’ experience in Quality Assurance/Quality Control, in the biopharmaceutical or pharmaceutical manufacturing industry (early-phase and/or commercial), thereof at least 2 years in a leadership position.
Experience with hosting foreign and domestic regulatory inspections (US-FDA, EU authorities, Health Canada)
Knowledge of cGMP requirements and experience in the application and interpretation of cGMP requirements for finished dosage forms.
Strong organizational skills.
Advanced problem-solving skills.
Advanced written and verbal communication skills.
Excellent interpersonal skills.
Strong leadership skills
Knowledge of available Office software systems including Word, Excel and Access.
Proven experience in pharmaceutical regulatory requirements.
Experience enables job holder to deal with the majority of situations and to advise others.

Additional Competencies

Results Orientation

Redesigns practices and processes for breakthrough results
Significantly improves organization’s practices, processes and quality
Senior fluency in quality risk management principles and risk tool usage, including strong ability to mentor others in Quality Risk Principles and workflows

Role Orientation / Strategic Orientation

Leads improvement areas, redesigns processes and manages QA activities with best practices
Supports definition of standards for quality systems and compliance
Supports Director, Quality with setting the annual QA priorities and defining specific plans, with team involvement
Facilitates cross-functional team activities
Leads collaboration within organization
Sets model for collaborative culture and leadership
Understands and commits to demonstrating high emotional intelligence (self-awareness, self-regulation, empathy, social skills, motivation) and demonstrates medium to high emotional intelligence
Commitment to support and develop peers, as applicable, with the goal to reach full potentials

Collaboration and Influence

Facilitates cross-functional team activities
Leads collaboration within organization
Sets model for collaborative culture and leadership
Understands and commits to demonstrating high emotional intelligence (self-awareness, self-regulation, empathy, social skills, motivation) and demonstrates medium to high emotional intelligence
Commitment to support and develop peers, as applicable, with the goal to reach full potentials

Technical Proficiency / Business-Focused Proficiency

Advanced supervisor level expertise with broad, advanced knowledge of GMP requirements for Manufacturing control, batch records review, upstream, downstream and/or filling operations and product release requirements and quality systems.
Advanced level expertise with broad, advanced knowledge of Quality Systems (Change Control, Deviations, Investigations, Root Cause Analysis, CAPA and Risk Assessments).
Demonstrates excellent judgement, technical competence and knowledge critically essential for the role.
Ability to coach and mentor QA team members and other department colleagues in their area(s) of expertise.
Demonstrates broad awareness and efficiency in addressing diverse business, quality and organizational challenges
Acts with integrity, values others’ perspectives, ensures transparent, collaborative action and communication, actively listens, commits to active listening, holds themselves accountable

Your Application

To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at www.evonik.com/en/careers.html.

Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations.

Your Talent Acquisition Manager:

Robin Rose

Company is

Evonik Canada Inc.

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More about this job

Responsibilities

The role involves maintaining QA procedures, overseeing GxP compliance, and performing batch record reviews and product disposition. It also requires managing change controls, CAPAs, and hosting customer audits to ensure high quality and regulatory standards.

Requirements

Requires a minimum B.S. degree in a scientific or engineering field with 10-12 years of QA/QC experience in the pharmaceutical industry. Candidates must have leadership experience and a proven track record of hosting regulatory inspections from agencies like the FDA and Health Canada.

Skills

Quality Assurance
cGMP Compliance
Batch Record Review
Change Control Management
CAPA
Root Cause Analysis
Quality Risk Management
Internal Auditing
Supplier Qualification
Validation Strategies
KPI Tracking
Leadership
Problem Solving
Technical Writing
Interpersonal Communication
Project Management

Benefits

Competitive Base Compensation
Bonus
Employer Paid Health Benefits
Employer Paid Dental Benefits
Wellness Education Sessions
Financial Planning Resources
Savings Plans
RRSP
Generous Vacation
Paid Time Off For Community Volunteer Activities
Financial Assistance For Fitness Memberships
Comprehensive Health Promotion Program
Ongoing Training And Development

Visa sponsorship

Not detected in the job text

Hiring contact

Robin Rose

Keywords

cGMP
GxP
CDMO
Lipid Nanoparticle
FDA
Health Canada
EU Authorities
OOS
Environmental Monitoring
Clean Utility Monitoring
Computer System Compliance
CSC
Quality Risk Management
Biopharmaceutical
Pharmaceutical Manufacturing
Analytical Method Validation
Cleaning Verification
Equipment Qualification
KPI
Microsoft Word
Microsoft Excel
Microsoft Access

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