Cell Culture Research Associate (Quality Control)

OCT Biopharma Inc.; City of Moncton; On-site; CAD 60,000 - 80,000; Full time

Job summary

A leading biopharmaceutical company in Moncton seeks a Cell Culture QC Associate. The role involves routine quality control testing, documentation per GMP standards, and collaboration across teams. Candidates should have a Master's degree in a scientific field and practical experience in QC. This position offers a competitive salary, health benefits, and opportunities for professional development in a cutting-edge research environment.

Benefits

Health insurance

Professional development opportunities

Casual and sick leave

Qualifications

• Minimum 1 year of practical experience in a QC or laboratory setting with a focus on mammalian cell culture.
• Familiarity with quality standards such as GMP or ISO 9001.
• Ability to follow SOPs and regulatory guidelines with high attention to detail.

Responsibilities

• Perform routine quality control testing of cell cultures including viability and contamination checks.
• Accurately document all QC testing activities in compliance with GMP standards.
• Collaborate with cross-functional teams to ensure product quality.

Skills

Aseptic technique

Standard tissue culture procedures

Basic data analysis

Organizational skills

Education

Master's degree in Biotechnology, Microbiology, or a related field

Tools

Excel

LIMS systems

Job description

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 opportunitiesOpportunities for growth and continuing education

To Apply

Please submit your CV to [e-mail]