18 of 18 GMP Jobs in the South East

technologies like ERP, LIMS, MES, RPA, or data analytics platforms. Knowledge of methodologies such as Agile, Waterfall, or hybrid delivery approaches. Awareness of pharmaceutical regulations and standards, including GxP, GMP, GDP, or equivalent. Proficiency in using business process modelling tools such as BPMN, Visio, ARIS, or Lucidchart. Robert Half Ltd acts as an employment business for temporary positions and an More ❯

as QA Manager will take ownership of Quality Assurance. Duties Lead and manage the QA team across the Abattoir and Boning Hall. Be responsible for delivering high levels of GMP, food safety and integrity standards within the factory. Support in driving food safety, compliance, and quality improvements across site. Update and maintain the QMS, conduct audits and ensure any corrective 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 ❯

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 ❯

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 ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Participate in Technical audits including customer and Group Technical, ensuring all relevant raw material information is available and completed in the required timescale Audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence, effectively communicated to enable the operational teams to take the appropriate and necessary corrective action & to follow More ❯

Unix-based operating systems, use of the command line and SQL is advantageous but not essential as training will be provided. * Strong knowledge of Contracting Out Requirements such as GMP * Strong Defined Benefit Knowledge, including historical knowledge of UK Pensions Legislation. Equal Opportunity Employer More ❯

transform, and cleanse member data Design and implement tools and processes to resolve client data issues Review and quality-check the technical work of others Support projects such as GMP reconciliation, rectification exercises, and data audits Manage multiple projects simultaneously, ensuring delivery on time and within scope About You Strong knowledge of DB pensions administration systems and their data structures 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 ❯

pension rectification projects. Location: London, Reigate, Bristol, Birmingham, Manchester, Leeds, or Edinburgh Work Style: Hybrid and flexible options available The Role: Design and tailor bulk data rectification approaches for GMP and other correction projects Communicate complex technical issues to various internal and client audiences Demonstrate sound judgement in balancing the need for accuracy and pragmatism in solutions Guide a team More ❯

Unix-based operating systems, use of the command line and SQL is advantageous but not essential as training will be provided. Strong knowledge of Contracting Out Requirements such as GMP Strong Defined Benefit Knowledge, including historical knowledge of UK Pensions Legislation. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy. More ❯

Excel Knowledge of technical actuarial concepts, specifically principles underlying bulk annuity pricing Awareness of DB buy in/buy out market, life insurance/relevant regulation. Any experience of GMP would be a distinct advantage Support Head of True up, DB Actuary and DB Senior Actuarial Analyst in accurate and timely delivery of data true ups. Carry out all necessary More ❯

the functioning of the QMS, providing oversight to key stakeholders alike (including senior staff members). Accountability across (but not limited to); change control, stability, documentation control, internal audits, GMP, supplier approval, complaints, PQRs, NPI, route cause analysis and controlled drug returns. Ensuring compliance/correct documentation practices, i.e batch records, laboratory tests and quality agreements too. Overseeing supplier verification … batch review process. Keeping abreast of evolving UK & EU retained regulations (for the purposes of pharmaceutical and/or food/ingredients manufacturing). To ensure compliance with EU GMP standards & BRC food safety requirements. Managing the preparation process (and heavily involved in hosting activities) for MHRA inspections, customer (third party audits) and acting as the lead person. Enrsuring quality … bodies. Deputising for the HOQ when required. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experience managing QA team/s in an GMP/Pharmaceutical setting. Management experience essential (will consider Team Leader or similar). Experienced in batch review and batch release Experience in auditing and audit hosting Experience in CAPA, deviations More ❯

We are seeking an experienced Quality Operative/GMP Co-ordinator to join … a leading food manufacturing business, ensuring products meet strict safety, hygiene, and compliance standards. In this MondayFriday role, youll carry out quality checks, support production teams, and maintain Good Manufacturing Practice across all processes. With steady hours, full PPE, and the potential to go permanent, this is a great opportunity to build on your food industry expertise. What Youll Be … Doing: Carrying out GMP and quality checks across production processes Collecting and testing product samples to meet exacting standards Conducting hygiene audits to maintain compliance Supporting and mentoring colleagues on quality procedures Printing and verifying labels for accuracy and compliance Working in a temperature-controlled environment (811C) to ensure product integrity What Were Looking For: Proven experience in quality within More ❯

product in a timely and cost effective manner. Analyse production data to identify trends, deviations, and performance metrics. Assist in the execution of cleaning validation protocols in line with GMP requirements. Bring in SQL/Power BI approaches to improve the site approach to data. Support sampling, documentation, and coordination of validation activities. Your Background : GMP experience is essential Have … degree (e.g., Biochemistry, Biotechnology, Chemical Engineering, Pharmaceutical Sciences). Understanding of cleaning validation principles and documentation practices. Experience with data handling and analytics Knowledge of HSE, bio-safety standards, GMP regulations as well as main tools and principles of operational excellence Company: Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one More ❯

product in a timely and cost effective manner. Analyse production data to identify trends, deviations, and performance metrics. Assist in the execution of cleaning validation protocols in line with GMP requirements. Bring in SQL/Power BI approaches to improve the site approach to data. Support sampling, documentation, and coordination of validation activities. Your Background : GMP experience is essential Have … degree (e.g., Biochemistry, Biotechnology, Chemical Engineering, Pharmaceutical Sciences). Understanding of cleaning validation principles and documentation practices. Experience with data handling and analytics Knowledge of HSE, bio-safety standards, GMP regulations as well as main tools and principles of operational excellence Company: Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one More ❯

We are seeking an experienced Quality Operative/GMP Co-ordinator to join … a leading food manufacturing business, ensuring products meet strict safety, hygiene, and compliance standards. In this MondayFriday role, youll carry out quality checks, support production teams, and maintain Good Manufacturing Practice across all processes click apply for full job details More ❯