Hobson Prior are looking for a QA Specialist (GMP)to join a top biotechnology organisation on a permanent basis in Stevenage. Our client concentrates on developing pioneering gene therapies to enable people living with chronic diseases live a better life.
Evaluate executed batch manufacturing records for compliance with GMP.
Responsible for QA approval of manufacturing PPM and calibration activities.
Perform room release checks prior to manufacturing activities.
In charge of compiling Product Specification Files (PSFs).
Review facility EM trends for approval by QA Manager (GMP).
Assist with internal & external audits of GMP manufacturing activities.
Main point of QA contact for all CGT-related GMP deviations and change control assessments.
Responsible for overseeing the receipt of biological raw materials.
Accountable for the approval/rejection of raw materials for use in manufacturing at CGT.
Assist with validation/qualification activities as required.
Excellent planning and organisational skills.
Ability to work in a small team in a dynamic environment.
Experience with biologics/ATMP.
Excellent interpersonal skills.
Excellent verbal and written communication.
Educated to degree level or equivalent in a scientific discipline.
Prior experience with the approval of raw materials.
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.