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Senior Bio-Process Engineer - Biologics Manufacturing

Job in Kimberley, Cranbrook / East Kootenay, BC, Canada
Listing for: Placements24
Full Time position
Listed on 2026-10-15
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 90000 - 130000 CAD Yearly CAD 90000.00 130000.00 YEAR
Job Description & How to Apply Below
Location: Kimberley

About the Role

Our client is seeking an experienced Senior Bio-Process Engineer to join their dynamic Biologics Manufacturing team in Kimberley. This role is essential for the development, optimization, and scale-up of bioprocessing operations for therapeutic proteins and other biological products. You will be instrumental in ensuring efficient, robust, and compliant manufacturing processes, contributing directly to the production of life-saving therapies. This position offers a challenging and rewarding opportunity to apply your engineering expertise in a growing and innovative pharmaceutical manufacturing environment, working collaboratively with production, quality, and R&D teams.

Key Responsibilities
  • Develop, optimize, and scale-up upstream and downstream bioprocessing operations for therapeutic proteins, vaccines, and other biologics.
  • Design and execute experiments to improve process yield, product quality, and cost-effectiveness.
  • Troubleshoot and resolve process deviations, ensuring adherence to Good Manufacturing Practices (GMP).
  • Author and review process development reports, batch records, and validation protocols.
  • Collaborate with cross-functional teams, including manufacturing operations, quality assurance, and regulatory affairs, to ensure successful process transfer and implementation.
  • Stay current with industry trends and emerging technologies in bioprocessing and biotechnology manufacturing.
Requirements
  • Master's or Ph.D. degree in Biochemical Engineering, Chemical Engineering, Biotechnology, or a related field.
  • Minimum of 6 years of experience in bioprocess development and/or manufacturing within the biopharmaceutical industry.
  • Strong understanding of upstream (cell culture, fermentation) and downstream (chromatography, filtration) processing technologies.
  • Experience with process scale-up, technology transfer, and process validation is essential.
  • Proficiency in relevant software tools for process modeling and data analysis.
  • Excellent problem-solving, communication, and project management skills, required for working in a hybrid capacity in Kimberley.
Benefits
  • Highly competitive salary and bonus program reflecting experience and contribution.
  • Comprehensive health, dental, and vision insurance plans.
  • Generous paid time off, retirement savings plan, and other employee benefits.
  • Opportunities for professional development, continuous learning, and career advancement.
  • A collaborative work environment with access to cutting-edge manufacturing technologies.
Position Requirements
10+ Years work experience
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