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Added 11 hours ago
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Senior Critical Environment Electrical Engineering
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Canada Impact+ Emerging Leader in AI-integrated Biomedical Devices
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be a registered professional engineer in Canada, or be eligible to apply for registration with the Engineers and Geoscientists of British Columbia (details available at www.egbc.ca);
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EHSS Officer
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EHSS Officer
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Burnaby, BC
- Full-time
Our success hinges on a diversity of ideas powered by people, not egos. Whether you’re a scientist or engineer, new to the team or established, in business, production, or anything in…

Evonik Oxeno

Plant Engineer

Burnaby, BC, Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 22, 2026
Posting language: English
Posted: Oct 22, 2026

Original job description

10/22/2026

Plant Engineer

Target Salary Range

$70,200 – $93,600 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

At Evonik, you’re part of a global chemical company working in many sectors that go beyond chemistry. From lipids for tomorrow’s medicines, biosurfactants for green detergents, additives for plastics recycling or membranes to help drive forward the energy transition, you’ll play an essential part in helping the world’s most essential industries succeed.

Our success hinges on a diversity of ideas powered by people, not egos. Whether you’re a scientist or engineer, new to the team or established, in business, production, or anything in between – we cheer each other on. Because we believe we can do anything. Explore everything. And Be Part of Something Special!

Find Out More About The Many Benefits We Offer

https://www.evonik.com/en/careers/why.html

Meet the team and get to know the people behind Evonik:

https://www.evonik.com/en/news/meet-the-team.html

Responsibilities

Execute assigned projects by effectively using Project Management methodologies in alignment with Good Engineering Practices (GEP).
Oversee and execute calibration activities for manufacturing equipment to ensure compliance with industry standards.
Implement maintenance schedules to maximize equipment reliability and minimize downtime.
Support commissioning, qualification, and validation (CQV) activities for new and existing equipment and processes and maintain appropriate documentation in accordance with regulatory requirements.
Collaborate with cross-functional teams to troubleshoot equipment/asset issues and implement effective solutions. Participate in root cause analysis and corrective action initiatives to address equipment failures or non-conformances.
Conduct regular inspections and audits of equipment and systems to ensure adherence to safety and quality standards.
Identify Continuous Improvement opportunities related to maintenance.
Read and review engineering drawings and provide technical input to design firms if necessary.
Follow SOP’s, cGMP, and GLP regulations and procedures; generate and maintain thorough and accurate documentation by using GDP in support of regulated activities.
Contribute to equipment design discussions and selection as directed by management.
Contribute to the development of site’s equipment strategy to ensure an optimal equipment life cycle is managed appropriately
Contribute to the site’s strategic capital projects
Responsible to meet fundamental cGMP requirements relating to conduct and work practices to ensure Safety, Identity, Strength, Purity, and Quality (SISPQ) of products manufactured at Vancouver Laboratories. This includes but is not limited to the following:
Initiate and/or support the creation and resolution of engineering related Deviations, CAPAs, and Change Controls.
Support with internal and client-driven audits during area inspections and follow-up observations
Review and approve maintenance reports.
Review and approve validation protocols.
Adhere to EHSS programs, rules, and procedures

Requirements

BS in a relevant Engineering field.
3+ years engineering/maintenance project execution and plant experience in a highly regulated industry, preferably the pharmaceutical or medical device industry.
Knowledge of FDA, ISO, ICH, EMA and Health Canada regulatory requirements and cGMP.
Knowledge of IT/OT and Computer System Validation is an asset
Knowledge and experience in the interpretation of GEP and ISPE standards.
Experience with risk assessments and mitigations, root cause analysis and risk/hazard/failure analysis.
Able to apply principles of Quality by Design, Design for Six Sigma, Lean Six Sigma, etc.
Experienced in the use of word processing, spreadsheet, and presentation software programs.
Effective written and verbal communication skills; ability to clearly and effectively communicate observations, results, and outcomes to more senior technical staff.
Conduct activities with consideration of budget, time schedules, and overall project goals and objectives.
Actively contribute to the improvement of policy, practices, and procedures.

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.

Apply now

Apply now

Job Details

Canada | Burnaby, BC

Full time

10/22/2026

Engineering

R52710

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Apply About employer

More about this job

Responsibilities

Execute engineering and maintenance projects, oversee equipment calibration and maintenance, and support commissioning, qualification, and validation activities. Maintain regulatory documentation and compliance, troubleshoot equipment issues, contribute to audits and corrective actions, and support equipment strategy and capital projects.

Requirements

A bachelor's degree in a relevant engineering field and at least three years of engineering or maintenance project execution and plant experience in a highly regulated industry are required. Candidates should know cGMP and relevant regulatory requirements, and have experience with risk assessment, root cause analysis, engineering standards, and continuous improvement methods.

Skills

Project Management
Equipment Calibration
Preventive Maintenance
Commissioning, Qualification, and Validation
Equipment Troubleshooting
Root Cause Analysis
Corrective and Preventive Actions
Continuous Improvement
Engineering Drawing Interpretation
Good Engineering Practices
cGMP Compliance
Good Documentation Practices
Risk Assessment
Quality by Design
Lean Six Sigma
Computer System Validation

Benefits

Competitive Base Compensation
Bonus
Employer-Paid Health Benefits
Employer-Paid Dental Benefits
Wellness Education
Financial Planning Resources
Savings Plans
RRSP
Vacation
Paid Time Off for Community Volunteering
Fitness Membership Assistance
Health Promotion Program
Training and Development

Visa sponsorship

Not detected in the job text

Hiring contact

Robin Rose

Keywords

Good Engineering Practices
cGMP
Good Laboratory Practice
Good Documentation Practices
FDA
ISO
ICH
EMA
Health Canada
IT/OT
Computer System Validation
ISPE Standards
Commissioning
Qualification
Validation
Calibration
Preventive Maintenance
Risk Assessment
Root Cause Analysis
Failure Analysis
Hazard Analysis
Quality by Design
Design for Six Sigma
Lean Six Sigma
Deviations
CAPA
Change Control
Capital Projects
Pharmaceutical Manufacturing

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