9 of 9 GMP Jobs in the South East

Root Cause Analysis using problem solving tools such as Fishbone, 5 Whys etc. Authors, reviews, and approves Controlled Documents in accordance with procedures. Will support in delivering the site GMP training as required. Will conduct the internal audit programme. Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required. … or supplier complaints are satisfactorily investigated and communicated. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experienced in batch review and batch release GMP QA experience is essential! Ideally in a Pharmaceutical setting or similar Experience in CAPA, deviations, change controls, internal auditing (preferred) etc Strong interpersonal skills, we are looking for Candidates who More ❯

systems. Your main accountabilities will include understanding and applying relevant standards so that Bakkavor, Customer and Legal requirements are achieved and maintained. This role is key to driving improved GMP Audits across the site. Role Accountabilities Understand and apply relevant standards and codes of practice so that Bakkavör, Customer, BRC and legal requirements are achieved and maintained. To ensure that More ❯

and embedded analytics for production KPIs Exposure to SAP IBP, PP/DS, or advanced scheduling tools is highly desirable Awareness of industry manufacturing standards and regulatory compliance frameworks (GMP, ISO, etc.) Stakeholder & Soft Skills Strong engagement skills with manufacturing stakeholders: Heads of Production, Plant Managers, and COOs Ability to translate complex operational processes into streamlined SAP-enabled solutions Excellent More ❯

z2bz0 years in programme/project management, ideally in pharmaceutical manufacturing or supply chain Strong background in managing large-scale planning or capital investment programmes Knowledge of GMP, tech transfers, regulatory frameworks, and operational readiness Skills: Excellent at critical path planning and integrated project time-lines Confident managing senior stakeholders and driving decisions Robert Half Ltd acts as an employment More ❯

looking for professionals with these required skills to achieve our goals: Degree level qualification (or strong equivalent experience) in an appropriate scientific, technical or engineering discipline. Thorough knowledge of GMP and Regulatory requirementsin a pharmaceutical environment. Thorough operational knowledge of manufacturing unit operations and plant/laboratory equipment Ability to communicate and influence effectively at all levels of the organisation 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 ❯

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 ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯