Quality Lead, Regenerative Medicine CDMO

Mytos & Aspen; Greater London; On-site; GBP 150,000 - 200,000; Full time

Job summary

A pioneering biotechnology firm is seeking an experienced Quality Assurance Lead to oversee compliance and lead the path to MHRA MIA licensing. As part of this role, you will establish quality protocols and ensure that production aligns with stringent regulations. The ideal candidate will have significant experience in quality assurance, a strong knowledge of MHRA and EU GMP, and thrive in fast-paced environments. This position offers a competitive salary along with benefits including stock options and opportunities for professional growth.

Benefits

Competitive salary

Stock options

Professional growth potential

Qualifications

• Significant QA experience is required.
• Strong knowledge of MHRA and EU GMP is essential.
• Ability to establish quality protocols is critical.

Responsibilities

• Oversee compliance and lead MHRA MIA licensing processes.
• Establish quality protocols in production.
• Ensure production aligns with stringent regulatory standards.

Skills

Quality Assurance experience

Knowledge of MHRA

Understanding of EU GMP

Ability to thrive in fast-paced environments

Job description

A pioneering biotechnology firm in Greater London seeks an experienced Quality Assurance Lead to oversee compliance and lead the path to MHRA MIA licensing. This role will involve establishing quality protocols and ensuring production aligns with stringent regulations. Ideal candidates have significant QA experience, strong knowledge of MHRA and EU GMP, and thrive in fast-paced environments. Competitive salary with benefits including stock options and professional growth potential.