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Added 5 mins ago
BC
Head of Lighting
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- Full-time
Banff Centre is looking for a Head of Lighting to provide the operational support required for the delivery of Banff Centre programs and activities. The Head of Lighting supports the aims…
Added 5 mins ago
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- Full-time
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Added 5 mins ago
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- Full-time
Current NAIT employees are welcome to apply for this opportunity. To be considered, please submit your application through the NAIT Jobs Hub rather than the external career site.
Added 5 mins ago
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- Full-time
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Added 6 mins ago
M
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Evonik

Scientist II

Burnaby, BC, Canada

Full-time

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Applications open in a new tab.

Job details

Job type: Full-time
Experience: With over 25 years of experience and having transacted business in about 50 different countries,
Posting language: English
Posted: Nov 4, 2026

Original job description

Target Salary Range:

$77,900 Minimum – $103,800 Mid 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

Support and/or lead the management of innovation projects in close collaboration with the business. The focus of the projects will be on the parenteral drug delivery field, in particular on LNPs and the delivery of genetic drugs.
Support and/or lead the establishment of new formulation capabilities through conducting experiments, characterizing new formulations, and performance testing of new formulations
Provide thorough tabulation, descriptions, and summaries of experimental methods, data, observations, results, and conclusions both verbally and written.
Support the maintenance of the designated lab space and applicable equipment
Perform other duties as assigned

REQUIREMENTS

BSc, MSc, or PhD in Biochemistry, Biology, Chemistry, or Pharmaceutical Sciences
Work experience: PhD - 0-2 years of work experience in R&D, Formulation or process development, or a related relevant field (pharmaceutical industry experience is an asset)BSc/MSc 3-5 years of work experience in R&D, Formulation or process development, or a related relevant field (pharmaceutical industry experience is an asset)
Advanced knowledge of the design and development of complex parenteral formulations such as microparticles, polymeric nanoparticles, lipid nanoparticles, polymeric implants, liposomes and micelles. Experience in the field is a plus.

Knowledge of design and interpretation of pharmacokinetics studies (in vitro and in vivo)

Experience in the Design of Experiments (DOE) and Quality by Design (QbD) principles for formulation development

Knowledge of the scientific principles pertaining to and capable in the operation of standard laboratory and/or processing and manufacturing equipment including mixing, emulsification, microfluidics, flow control, drying, hot melt extrusion, spray drying, data collection, etc.

Knowledge of the scientific principles pertaining to and capable of data interpretation of analytical data including HPLC, UV/Vis spectrophotometry, particle size, IVR, viscometry, DSC, TGA, etc.

Knowledge and capability of executing documentation requirements associated with pharmaceutical development (e.g. laboratory documentation, development reports, specifications, protocols, batch records, etc.)

Able to work with minimal supervision in a multidisciplinary team environment

Must possess strong problem solving, organizational and documentation skills with a focus on details and results

Good mathematical and computer skills. Proficiency with MS Word, Excel, Power Point and Visio

The candidate should be self-motivated and possess good interpersonal, collaborative, and communication skills.

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 About employer

More about this job

Responsibilities

The Scientist II will support and lead innovation projects focused on parenteral drug delivery, specifically involving lipid nanoparticles and genetic drugs. They are responsible for establishing new formulation capabilities, conducting experiments, and maintaining laboratory equipment and documentation.

Requirements

Candidates must hold a BSc, MSc, or PhD in Biochemistry, Biology, Chemistry, or Pharmaceutical Sciences with relevant R&D or formulation experience. Proficiency in complex parenteral formulation development, analytical techniques, and GMP documentation standards is required.

Skills

Parenteral drug delivery
Lipid nanoparticles
Formulation development
Process development
Analytical method development
Design of experiments
Quality by design
HPLC
Particle size analysis
GMP compliance
Microfluidics
Data interpretation
Technical documentation
Problem solving
Collaboration
Communication

Benefits

Competitive base compensation
Bonus
Health benefits
Dental benefits
Wellness education sessions
Financial planning resources
Savings plans
RRSP
Generous vacation
Paid time off
Fitness membership assistance
Comprehensive health promotion program
Training and development

Visa sponsorship

Not detected in the job text

Hiring contact

Robin Rose

Keywords

Scientist
Parenteral drug delivery
Lipid nanoparticles
CDMO
CMC services
Formulation design
Process development
Scale-up
GMP
Analytical method development
HPLC
Design of experiments
Quality by design
Microfluidics
Biochemistry
Pharmaceutical sciences
Pharmacokinetics
DSC
TGA
Viscometry
Batch records
Laboratory documentation
R&D
Liposomes
Polymeric nanoparticles
Emulsification
Flow control
Spray drying
Hot melt extrusion
Data collection

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