QA, Quality, GMP, audit, QMS, batch, documentation
Your new company
This award winning biopharmaceutical based in Cambridge is at the forefront of the gene editing industry. They engineer modified cells that are applied to research and have a rapidly growing line of products that advance human health. The company also have a strong R&D pipeline and are looking to rapidly expand. They have recently undergone numerous acquisitions that have resulted in increased headcount.
They are looking to strengthen their Global Quality team through the appointment of a QA Specialist at their site based in Cambridge.
Your new role
Your new job role as QA Specialist will be to lead the QA activities onsite including production documentation and assisting with batch and product release. You will also ensure regulatory and quality requirements are met at all times. You will take part in internal/external audits and support deviations/ CAPAs and carry out SOP activities. Validation preparation will also be part of this position; protocols and reports. Reviewing QMS will also be part of your role.
What you'll need to succeed
In order to be considered for this Senior QA Officer position you will need previous experience in working in a similar position and carrying out the QA activities such as QMS, Validation, batch/ documentation.
Outstanding written and oral skills are needed as well as the ability to work well within a dynamic team whilst using your initiative. You will also have knowledge of Microsoft tools.
In return for this you will be given the opportunity to develop in a leading biopharmaceutical company, along with a competitive salary and benefits package.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.