A well-established company are searching for a Qualified Person to join the team on a permanent basis. This is a fantastic opportunity for a motivated individual to join who has great communication skills. The role will involve a variety of different job responsibilities and will involve assisting in the delivery of autonomous and innovative Quality management.
Qualified Person – Job Description:
To review batch manufacturing documentation to ensure compliance with EU GMP and the Product Specification File
To undertake audits in EU and third countries to ensure that sponsor manufacturing sites are operating in general compliance with EU GMP
To certify Medicinal products for use in the EU and outside the EU (where relevant)
To review company project files (PSFs, commercial project files etc.) to ensure compliance with the current regulatory requirements and procedures.
Qualified Person – Role Requirements:
Extensive QA experience within the medicinal products/pharmaceutical industry
Communication and stakeholder relations
Strong leadership qualities
Willingness to undergo security checks as appropriate
Please apply here or contact Hattie at X4 Life Sciences by ringing (phone number removed) or emailing if you wish to find out more information about the role.
If this role is not quite what you are looking for but would be interested in hearing about new job opportunities please don’t hesitate to contact myself. I have recently moved into the Quality & Regulatory team within X4 Life Sciences and I purely specialise in placing Quality and Validation Professionals on a permanent basis in the Pharmaceutical industry. Please feel free to get in contact with myself and you can find me on LinkedIn below.
Job Type: Permanent
To apply for this job please visit www.cv-library.co.uk.