Quality (QA) Lead - CDMO

Join Mytos, a revolutionary biotech company, as a Quality Assurance Lead to help scale cures to patients faster. You'll work with a world-class team to ensure quality moves in hand with business vision, collaborating with advisors and establishing quality at the world's first automated CDMO for Regenerative Medicine.

Requirements

• Significant QA experience (>5 years) in a GxP environment, ideally in ATMPs, biologics, or cell therapy
• Strong understanding of MHRA and EU GMP, with hands-on experience preparing for inspections
• Experience with PQS systems covering document control, deviations, CAPA, change control, validation, and training
• Meet MHRA requirements to be a Quality Controller on the MIA(IMP) license
• Experience in auditing and being audited
• Comfortable working in a fast-paced environment
• Excellent written and verbal communication skills

Benefits

• Competitive salary with stock options
• Lunch covered daily
• Collaborative team environment with high potential to learn new skills
• 24 days holiday (excluding bank holidays)
• Pension