in technology recruitment across niche markets including Information Technology, Digital TV, Digital Marketing, Project and Programme Management, SAP, Digital and Consumer Electronics, Air Traffic Management, Management Consultancy, Business Intelligence, Manufacturing, Telecoms, Public Sector, Healthcare, Finance and Oil & Gas. More ❯
Corsham, Wiltshire, United Kingdom Hybrid / WFH Options
Experis
in technology recruitment across niche markets including Information Technology, Digital TV, Digital Marketing, Project and Programme Management, SAP, Digital and Consumer Electronics, Air Traffic Management, Management Consultancy, Business Intelligence, Manufacturing, Telecoms, Public Sector, Healthcare, Finance and Oil & Gas. More ❯
in technology recruitment across niche markets including Information Technology, Digital TV, Digital Marketing, Project and Programme Management, SAP, Digital and Consumer Electronics, Air Traffic Management, Management Consultancy, Business Intelligence, Manufacturing, Telecoms, Public Sector, Healthcare, Finance and Oil & Gas. More ❯
Quality Assurance (QA) Validation- Contract Role (Sterile Pharma, Swindon - Onsite) Your new company A leading pharmaceutical organisation specialising in sterile manufacturing is seeking a skilled QA Validation expert to support a high-impact project. With a strong commitment to quality and regulatory compliance, this company offers a dynamic and collaborative environment for experienced contractors. Your new role As a Quality … you will serve as a Document Reviewer for Commissioning, Qualification, and Validation (CQV) activities. You'll be responsible for reviewing technical documentation related to equipment used in sterile pharmaceutical manufacturing, ensuring alignment with cGMP, FDA, and EMA standards. You'll collaborate with cross-functional teams to identify gaps, recommend corrective actions, and support continuous improvement efforts. What you'll need … to succeed Experience in a quality assurance validation role within sterile pharmaceutical manufacturing Strong knowledge of FDA, EMA, and cGMP regulations Exceptional attention to detail and analytical skills Proficiency in document management systems and quality management software Excellent communication skills and the ability to work independently Familiarity with risk-based validation approaches What you'll get in return A More ❯
