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Scientist - Product Development, Therapeutics

Vancouver, BC · Science/Research

Title: Scientist - Product Development, Therapeutics
Location: Greater Vancouver, BC
Employment Type: Full-time, Permanent
Schedule: Onsite, Monday to Friday, 8-hour workdays
Reporting to: VP, R&D
Compensation: $85,000 - 110,000 Base Salary

Ready to drive life-changing therapies through monoclonal antibody and vaccine development? Looking for a new challenge in an innovative, collaborative biotech company making a real impact?

Company Overview

Our client, a leading biotechnology company based in Greater Vancouver, focuses on developing innovative monoclonal antibody and vaccine therapeutics to address global health challenges such as infectious and autoimmune diseases. With a collaborative and fast-paced culture, this company is ideal for professionals passionate about driving innovation in healthcare and creating transformative solutions.

If you’re a self-motivated team player who thrives in a dynamic environment and enjoys tackling complex challenges, this role is for you.
Scientist – Product Development, Therapeutics

Position Summary

As a Scientist in Monoclonal Antibody and Vaccine Therapeutics Development, you will drive innovation by advancing the company’s pipeline of antibody-based therapies and next-generation vaccines. You will lead experimental research, optimize therapeutic and vaccine-related assays, and solve production challenges, ensuring the development of effective, high-quality monoclonal antibody products and vaccines.

Your expertise in antibody characterization, vaccine development, assay optimization, and problem-solving will be critical to advancing the pipeline of therapeutic products targeting infectious diseases, autoimmune conditions, or inflammatory disorders. This role requires a detail-oriented, independent thinker with a deep understanding of virology and immuno-based therapeutics.

Key Responsibilities

  • Design, plan, and execute experiments and assays independently to support the development of monoclonal antibody products and vaccines.

  • Enhance and refine assays for antibody and vaccine development (e.g., ELISA, cell-based functional assays, neutralization assays, potency assays, immunogenicity testing, and pharmacokinetic (PK) and pharmacodynamic (PD) studies) to ensure robust and reliable performance.

  • Ensure compliance with ISO 13485 for quality management systems, ICH Q6B for specifications and testing, and ICH Q5A for viral safety.

  • Contribute to standardizing laboratory procedures in line with ICH Q8 for pharmaceutical development and ICH Q9 for quality risk management.

  • Collaborate with regulatory and quality teams to support risk management activities in accordance with ISO 14971 and GMP standards.

  • Participate in validation studies to confirm monoclonal antibody and vaccine performance standards and ensure compliance with ICH Q2 for method validation.

  • Characterize monoclonal antibodies and vaccines through binding, specificity, immunogenicity, and functional assays to support clinical and regulatory submissions.

  • Analyze and summarize data critically, generating comprehensive reports and presentations for internal and external stakeholders.

  • Provide technical guidance to troubleshoot and resolve issues, mentoring junior staff as needed.

  • Develop a thorough understanding of virology’s role in autoimmune and infectious diseases and its integration into monoclonal antibody and vaccine therapies.

  • Manage laboratory operations, including equipment maintenance and adherence to safety protocols.

Qualifications and Experience

  • MSc or PhD in Virology, Immunology, Biotechnology, or a related life sciences field, with at least 5 years of industry experience in monoclonal antibody or vaccine development.
  • Experience and familiarity with ISO 13485, ISO 14971, ICH Q5A, ICH Q6B, and ICH Q2 standards, as well as GMP/GLP guidelines for therapeutic and vaccine validation
  • Experience with hybridoma and recombinant antibody technologies is an asset.
  • Knowledge of vaccine platforms such as mRNA, protein subunit, or viral vector-based systems is an asset.
  • Exceptional communication, coordination, and problem-solving skills.
  • Demonstrated ability to prioritize multiple tasks and excel in a fast-evolving environment
  • Legal authorization to work in Canada.
#MonoclonalAntibodies #VaccineDevelopment #BiotechJobs #TherapeuticDevelopment #Virology #SeniorScientist #LifeSciences #R&DJobs #AntibodyTherapeutics #BiotechNorthAmerica #DrugDevelopment #Biologics #BiotechHiring #Vancouver #TalentSphere

 #VaccineDevelopment #AntibodyTherapeutics #Biologics #TherapeuticDevelopment #BiotechJobs #Virology #R&DJobs #LifeSciences #ClinicalResearch #BiotechCareers #LabTechnician #GMPJobs #PharmaceuticalJobs #Vancouver #TalentSphere
Contact Carla Campbell, TalentSphere  - Life Sciences at ccampbell@talentpshere.ca for further information on this opportunity.


TSSHP LI-TS1
Job Posting ID (#16606077)

 


Thank you for your interest in this job posting.

We look forward to hearing from you.

TalentSphere Staffing Solutions
talentsphere.ca

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