10 of 10 GMP Jobs in the South East

Key responsibilities: Supporting the Head of QA & RA, QA Managers, Responsible Persons and Qualified Persons with the implementation and maintenance of the Quality Management System in accordance with the GMP and GDP guidelines and GPhC, ISO 9001 and ISO 13485 standards. Supporting the ongoing compliance with relevant standards, legal requirements, regulations and the PSDL documented policies and procedures. Promoting a … of the Quality standards required and able to promote a positive Quality culture within the company. Excellent knowledge of Word, Outlook, Excel, PowerPoint, and Teams. Good knowledge of GDP, GMP and GPhC regulations, ISO 9001 and ISO 13485 standards. More ❯

intermediate product release while maintaining an efficient service in line with customer demands for the release of manufactured batches. Give advice and assistance across site on a range of GMP topics. May be expected to carry out GMP or corrective training. Review and approve documents as the Quality representative such as SOPs and technical reports. Support validation document review and More ❯

team in Milton Keynes. As a senior contributor, you'll lead the design and implementation of cutting-edge process control systems-PLC, DCS, HMI, SCADA-for a high-performance, GMP-regulated manufacturing environment. This is an exciting opportunity to make a direct impact on the setup and development of a new facility, work on high-value capital projects, and support More ❯

team in Milton Keynes. As a senior contributor, you'll lead the design and implementation of cutting-edge process control systems-PLC, DCS, HMI, SCADA-for a high-performance, GMP-regulated manufacturing environment. This is an exciting opportunity to make a direct impact on the setup and development of a new facility, work on high-value capital projects, and support 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 ❯

extensive and successful work with RNA manipulation, RNA constructs and a good understanding of transcriptomics and/or viral genomics is essential. Experience in RNA-related biopharma methodologies or GMP is also desirable. The role also requires 2-3 years of prior managerial experience overseeing experimental work of junior team members. We encourage the successful candidate to liaise with senior … QC data and sequencing data to support sample prep methodologies as they are developed and investigated Working with relevant partners to deliver methodologies congruent with Q-line and regulatory GMP practices What We're Looking For We will expect you to have a PhD and postdoctoral experience (or equivalent experience) in a molecular biology/biotechnology-based field, and/ More ❯

to working in a customer-focused service business. Accuracy and attention to detail. Excellent customer service and communication skills. Good written and arithmetic skills to comply with audits and GMP standards. Understanding of GMP/GLP standards. Ability and confidence to work alone on a customer site without supervision and as part of a multi-disciplined team. BSc or equivalent More ❯

as Studio5000 & FactoryTalk Software especially FT View SE, FT Batch). Knowledge of Batch Process Control, ISA-S88 standard programming. Knowledge of GAMP, 21 CFR Part 11, ASTM E2500, GMP, etc Knowledge of Virtualisation technology. What We Offer: Comprehensive mindfulness programs with a premium membership to Calm Volunteer Paid Time off available after 6 months of employment for eligible employees More ❯

development life cycle methodologies, 21 CFR Part 11, and GAMP. Development of detailed specification, engineering documents, SOP and operating standards. Ownership and administration of process control automation in a GMP regulated manufacturing setting. Lead technical root cause analysis, incident investigations, and troubleshooting on process control issues related to electrical, instrumentation and control systems. Design and test of newly installed and More ❯

business areas, processes, functions. Excellent initiative and self-management skills as well as ability to lead teams, influence others and manage conflict. Experience working in a regulated industry (i.e. GMP) and delivering within that environment. Desire and ability to operate at multiple levels (detail and strategic). Excellent communication skills, using a variety of methods in diverse forums. Desire and More ❯