Overview:
Our client, a leading CDMO specialising in biologics and sterile manufacturing is hiring an Associate Director, GxP Quality to oversee QA operations across multiple client projects. This remote-friendly role includes regular travel to European sites.
Key Responsibilities:
Act as the senior QA lead for audits and regulatory inspections
Provide strategic QA input across tech transfer and manufacturing
Lead risk assessments and quality KPI implementation
Mentor junior QA staff and harmonise quality systems across locations
Requirements:
10+ years in GxP quality roles, ideally within CDMO or biotech
Strong track record in audit management and regulatory engagement
Willingness to travel across Europe
Why Join?
Join a global CDMO with cutting-edge manufacturing capabilities and diverse client base
Influence quality standards across complex, multi-site operations
Flexible remote setup with regular international collaboration
Highly competitive compensation, travel allowance, and leadership opportunities
Equal Opportunities Employer
Axion is an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
We specialise in recruitment across multiple sectors – let’s talk.
