GMP QA Associate II – Cell Therapy Compliance

OmniaBio; Hamilton; On-site; CAD 75,000 - 85,000; Full time

Job summary

A biotechnology company is looking for a Quality Assurance Associate II on an 18-month contract. This role involves ensuring compliance with GMP for cell and gene therapy production, conducting audits, and collaborating with manufacturing teams. Candidates should have a bachelor's degree in science and 4-6 years of experience in related fields. The position demands strong leadership, analytical skills, and a detailed understanding of GMP regulations. The successful candidate will engage with clients and contribute to maintaining high-quality standards.

Qualifications

• 4-6 years of experience in GMP production within relevant industries.
• Knowledge of cell manufacture processes and technologies.
• Excellent communication skills for auditing and client interactions.

Responsibilities

• Deliver quality-related services to clients.
• Collaborate with teams for quality compliance.
• Conduct internal audits and participate in client audits.

Skills

Experience in cell therapy/viral quality

Understanding of GMP regulations

Leadership experience

Analytical skills

Detail-oriented

Education

Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology)

Master’s degree preferred

Job description

A biotechnology company is looking for a Quality Assurance Associate II on an 18-month contract. This role involves ensuring compliance with GMP for cell and gene therapy production, conducting audits, and collaborating with manufacturing teams. Candidates should have a bachelor's degree in science and 4-6 years of experience in related fields. The position demands strong leadership, analytical skills, and a detailed understanding of GMP regulations. The successful candidate will engage with clients and contribute to maintaining high-quality standards.