6 of 6 GMP Jobs in the East of England

Importance Extensive experience in facilities management, focusing on support services and operations Essential Strong track record in contract management, supplier performance monitoring, and budget oversight Essential Extensive knowledge of GMP catering contract models Essential Proven ability to lead security, soft services, insurance administration, and business continuity functions Essential Strong experience in Soft FM and building management Essential Extensive experience in More ❯

sufficient for an individual to meet the requirements of the role. Required Skills/Experience Process Automation : Experience in automation within the biopharmaceutical or pharmaceutical industry or another industry. GMP experience required. Good understanding of the biopharmaceutical/pharmaceutical development process. Expertise in commissioning and validation of automation systems. Understanding of device networking and communication protocols. Experience in installing and More ❯

of quality excellence across the business. Conducting supplier audits, internal inspections, and management reviews. Key Requirements: Proven experience in a GMDP or similar regulated environment. Strong knowledge of GDP, GMP, ISO 9001, and ISO 13485 standards. Excellent organizational, communication, and stakeholder management skills. A positive attitude toward promoting quality across all departments. Proficiency in MS Office applications (Word, Excel, PowerPoint More ❯

that the relevant documents have been completed, e.g., hold log, non-conformance log. Reporting any complex issues to QA Supervisor. Hygiene Audits, micro swabbing, and micro sampling product Formal GMP and Process Control document completion About the shift pattern: This Monday - Friday QA role is based in our technical department but working in all areas of the factory as required More ❯

that the relevant documents have been completed, e.g., hold log, non-conformance log. Reporting any complex issues to QA Supervisor. Hygiene Audits, micro swabbing, and micro sampling product Formal GMP and Process Control document completion About the shift pattern: This Monday - Friday QA role is based in our technical department but working in all areas of the factory as required More ❯

at East Suffolk and North Essex NHS Foundation. You will be based at Colchester Hospital, however you will be required to work across at Ipswich Hospital. You will have GMP experience within a pharmaceutical manufacturing facility. You will be a team player, joining an established department with a multi-disciplinary team. Our team have various professional scientific backgrounds, including different … licence, performing Quality Control analysis on raw materials and manufactured products, and maintaining Quality Assurance functions within Pharmacy Technical Services in line with Standard Operating Procedures and current Good Manufacturing Practice (cGMP) requirements. You will be expected to support the Pharmacy Quality Assurance team in ensuring that the regulatory requirements and standards set by the Medicines and Healthcare products Regulatory … Job description Job responsibilities For full details of the responsibilities and duties of this role please see the attached job description. Person Specification Experience Essential Previous experience of pharmaceutical GMP in NHS manufacturing unit or pharmaceutical industry as required by MHRA guidance for specials manufactures for batch release Demonstrated experience of multi- disciplinary working Handling of high risk medicines Desirable More ❯