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Associate II, GMP Manufacturing

Date: Sep 13, 2022

Location: Burnaby, British Columbia, CA

Company: Evonik Industries AG

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Associate II, GMP Manufacturing



Location: Burnaby, BC

Legal Entity: Evonik Canada Inc.

Business Line: Health Care



Evonik offers excellent benefits such as competitive compensation, benefit & pension plans, vacation and time off, and many wellness resources. 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! Why Vancouver?

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.   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.

Click here for a sneak peak of Evonik’s contribution to the COVID vaccine and how you could have a direct impact in helping our community

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  •  Supports Drug Product manufacturing in cleanroom environment according to appropriate GMP regulations and legal requirements (FDA, EU, Health Canada).
  • Executes preparation and compounding activities to manufacture Drug Products. Participates in core processes to support fill/finish activities.
  • Operates a variety of cleanroom and processing equipment including but not limited to autoclave, pumps, mixing vessels and particle monitoring systems.
  • Uses aseptic technique to minimize the risk of contamination when working in classified cleanroom environments.
  • Applies appropriate disinfection or sanitization methods to ancillary components and batching support materials.
  • Samples raw materials, active pharmaceutical ingredients and in-process control.
  • Performs cleaning, environmental monitoring and utility sampling associated with the maintenance and operation of the cleanroom.
  • Participates in the inspection, labeling, packaging and storing of Drug Products vials.
  • Documents GMP Manufacturing activities by completing forms, reports, logs, and records of equipment and batches.
  • Participates in opportunities for continuous improvement of core GMP Manufacturing processes.
  • Learns and follows SOPs, health and safety policies and GMP regulations through independent study and on-the-job training.




  • 2-5 years of experience working in manufacturing under current Good Manufacturing Practices or regulated environment.
  • Diploma or recognized qualification in a technical/science field.
  • Experience working in a cleanroom is preferred. Knowledge of aseptic technique is a definite asset.
  • Mechanical aptitude is preferred.
  • Able to work with minimal supervision in a multidisciplinary team environment.
  • Strict adherence to policies and procedures and ability to learn new techniques quickly and skillfully.
  • Strong attention to detail and commitment to right-first-time
  • Intermediate level of Microsoft Office applications.
  • Strong written and verbal communication skills.
  • Flexible work hours and schedule.  May be rquired to perform shift work to meet manufacturing requirements 

Your Application

To ensure the fastest process of your application and to protect the environment, please apply online via our careers portal at  referencing VACANCY REFERENCE NUMBER 147414

Evonik Corporation is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, gender, sexual orientation, national origin, disability status, protected veteran status or any other legally protected status.

Please note that Evonik will not accept any unsolicited application documents sent by staffing firms. Evonik works in conjunction with preferred service providers and will not pay any fee to staffing firms in the absence of an appropriate framework agreement. Should Evonik receive a candidate profile from a staffing firm with which it has no framework agreement, and should this candidate subsequently be considered in the recruitment process or offered employment, no claims from the staffing firm will be entertained in this regard.