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"We are currently looking for a Senior QA Specialist to join a leading Bio-Pharmeceutical company based in the Berkshire area.<br /><br />KEY DUTIES AND RESPONSIBILITIES: <br /><br />Your duties as the Senior QA Specialist will be varied however the key duties and responsibilities are as follows:<br /><br />1. Utilise knowledge of GMP and quality processes within the functional areas to Manage and escalate Major and Critical compliance issues through the site QMS processes e.g. deviations and CAPAs<br /><br />2. To provide shoulder to shoulder review, approval and support for the management of quality records e.g. Deviations, CAPA, Change Controls, Investigations<br /><br />3. Provide QA Technical support to key business partners for the management of quality records e.g. Deviations, CAPA, Change Controls, Investigations<br /><br />4. Maintain and promote a state of audit readiness<br /><br />ROLE REQUIREMENTS:<br /><br />To be successful in your application to this exciting opportunity as the Senior QA Specialist we are looking to identify the following on your profile and past history:<br /><br />1. Relevant degree in a  science related subject<br /><br />2. Proven industry experience in Quality assurance working to GMP regulatory standards<br /><br />3. A working knowledge and practical experience with supply chain - manufacturing. <br /><br /><br />Key Words: GMP, QA, Quality Assurance, Biologics, pharmaceuitcal, sterile, ATMP, FDA, Team lead, Biopharmaceutical, QMS, GxP<br />"
<https://jobs.chemistryworld.com/job/33950/senior-qa-analyst/>