Well Established Pharmaceutical CMO is Seeking to add to the Quality Team by Recruiting a Quality Assurance Officer, who Will Work Full Time, On-Site, at a State-of-the-Art Facility in a Highly Conducive Environment ROLE Controlling and Amending Master BPR’s and BAR’s Preparation of Product Quality Reports Controlled Document Management Authoring and Reviewing Controlled Documents eg Manufacturing Logs, SOP’s Reviewing and Approving Batch Record BOM’s, (Work Orders) Vendor Management, Collection of Required Quality Documents Management of Technical Agreements Artwork Proofing and Management, Including Liaison with Regulatory Affairs and Third Parties Risk Assessments and Gap Analysis Managing Monthly KPI’s Contributing and Assisting in Regulatory Inspections and External Audits Raising and Assessing Deviations, Change Controls and CAPA’s Reviewing Specifications, Methods and Ensure Effectiveness Handling Supplier Complaints Reviewing BOR’s to Ensure Conformance with Registered Licenses Ensuring Self-Inspections are Performed at Appropriate Regular Intervals, and Necessary Corrective Measures Introduced Supporting Regulatory Team, with Compilation of CTD Modules, Prior to MHRA Submissions Ensuring Established Quality Management System is Maintained and Sufficient for Accreditations Held REQUIRED Bachelor’s Degree (or Equivalent) in Relevant Field Minimum 3 Years QA Experience, Working in the Pharma Sector Sound Knowledge of Quality Assurance Terminology, Methods, and Tools Excellent Computer Skills, Including Database Management Analytical, Problem-Solving, and Decision-Making Skills