Cell Culture Research Associate

1 week ago

Moncton, New Brunswick, Canada OCT Biopharma Inc. Full time

Location:
Moncton, New Brunswick, Canada

Job Type:
Full-Time In-Person

Department:
Quality Control / Quality Assurance

Reports To:
QC Manager / Senior QC Scientist

Job Summary:

We are seeking a detail-oriented and proactive
Cell Culture QC Associate
with
1 year of hands-on laboratory experience
to support our Quality Control team. This role focuses on executing and documenting cell-based assays to ensure the integrity, consistency, and compliance of products and materials used in research or biomanufacturing.

Key Responsibilities:

  • Perform routine quality control testing of cell cultures including viability, morphology, and contamination checks (e.g., mycoplasma, endotoxin, sterility)
  • Maintain and monitor control cell lines and reagents used for QC assays
  • Conduct functional cell-based assays to assess potency, identity, and other critical quality attributes
  • Assist in the qualification, calibration, and maintenance of lab instruments (e.g., incubators, biosafety cabinets)
  • Accurately document all QC testing activities in compliance with GMP standards
  • Support data analysis, deviation reporting, and investigation processes
  • Participate in the development and revision of SOPs, protocols, and other QC documents
  • Collaborate with cross-functional teams (e.g., Production, QA, R&D) to ensure product quality and release timelines

Qualifications:

  • Master's degree in Biotechnology, Microbiology, or a related scientific discipline
  • Minimum 1 year of practical experience
    in a QC or laboratory setting with a focus on mammalian cell culture
  • Proficient in aseptic technique and standard tissue culture procedures
  • Familiarity with quality standards such as GMP or ISO 9001
  • Strong documentation and organizational skills
  • Ability to follow SOPs and regulatory guidelines with high attention to detail
  • Basic data analysis and reporting skills using Excel or LIMS systems

Preferred Qualifications:

  • Experience with cell-based potency assays, ELISA, or flow cytometry
  • Familiarity with electronic lab notebooks (ELNs) and/or quality management systems (QMS)
  • Understanding of ICH, or Health Canada regulatory expectations

Working Conditions:

  • Work primarily in a cleanroom or biosafety level 2 laboratory
  • Regular handling of biological materials and reagents under sterile conditions
  • 6 day week and occasional overtime work may be required based on project needs

Compensation and Benefits:

  • Opportunity to work in a cutting-edge research environment
  • Contribute to significant advancements in therapeutic research
  • Competitive salary based on experience
  • Health, dental, and vision insurance
  • Casual and sick leave
  • Professional development opportunities
  • Opportunities for growth and continuing education

To Apply:
Please submit your CV to

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