26 to 39 of 39 GMP Jobs

impact digital transformation projects in the Pharmaceutical industry? This opportunity offers the chance to work on cutting-edge MES implementations and validation strategies within GMP-regulated environments in the UK. Due to upcoming project needs, we are looking for a Senior Consultant – MES & Validation (Siemens Opcenter Execution Pharma … Opcenter Execution Pharma Contribute to the definition of Validation Master Plans and overall validation strategy Review and assess validation documentation to ensure compliance with GMP requirements and project standards Evaluate the system integrator’s project methodology and assess the quality and consistency of deliverables Ensure alignment with project expectations, regulatory ...

Accentuate Staffing is partnering with a leading pharmaceutical manufacturing organization to identify a Technical Writer to support documentation and compliance efforts within a GMP-regulated environment. This individual will play a key role in developing, editing, and maintaining critical documentation to support quality, validation, and manufacturing operations. The ideal candidate … maintain technical documentation including SOPs, work instructions, validation protocols, and reports Collaborate with Quality, Manufacturing, and Engineering teams to ensure documentation aligns with GMP standards and operational processes Support documentation related to validation activities, including process, equipment, and cleaning validation Ensure all documentation meets regulatory requirements (FDA, cGMP) and internal ...

quality, and regulatory compliance. You will be responsible for maintaining high quality and compliance standards across the business, ensuring all products meet regulatory and GMP requirements. Sector – Pharmaceutical Manufacturing Non-Negotiable Requirements of the QA Officer Previous QA experience Experience working within a pharmaceutical or regulated environment Requirements … background Experience supporting regulatory submissions Knowledge of batch record review and product quality reviews Experience working with Quality Management Systems (QMS) Strong understanding of GMP and regulatory standards (MHRA, ISO) Experience with documentation control and SOP writing Ability to manage deviations, CAPAs, and change controls Strong attention to detail ...

product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder … Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft applications) Good interpersonal skills ...

PAYE | £42 UMB Overview: We’re looking for a detail-oriented System Specialist to manage and support our Document Management System (DMS) within a GMP pharmaceutical environment. This role will focus on document lifecycle management, system coordination, and supporting a migration to Veeva Vault. Key Responsibilities: Manage … validation docs) Act as DMS Super User: workflows, permissions, master data, and reporting Support DMS cleanup and migration activities Monitor periodic reviews and ensure GMP compliance Coordinate document translations across global teams Provide user support, training, and troubleshooting Requirements: Degree in Life Sciences or related field 3+ years in document ...

quality within a regulated environment. You'll play a key role in ensuring products are manufactured and distributed to the highest standards, supporting GMP compliance, managing quality documentation, and working closely with cross-functional teams to resolve issues and drive continuous improvement. The Role Promote GMP and quality standards across … distribution Inspect, sample and approve incoming materials and packaging Review batch records and support product release Investigate deviations, non-conformances and CAPAs Maintain accurate GMP and quality documentation Support shop floor compliance through audits, checks and training Assist with complaints investigations and root cause analysis Work closely with Production, Supply ...

providing control system engineering support to troubleshoot, maintain and improvement projects of Automation and Controls systems for the Automated Equipment in a dynamic GMP regulated environment, requiring minimal downtime of the machinery. Responsibilities include fast response for troubleshooting to sustain machinery uptime when unscheduled downtime occurs, identification of improvements … develop the necessary contingency plans to improve business continuity. Performs troubleshooting and modifications to the automated equipment adhering to Pharmaceutical and Medical Devices GMP change control standards and policies. Creates and modifies system specifications and standard operating procedures for the systems supported. Trains users and peers on systems. Supports software ...

providing control system engineering support to troubleshoot, maintain and improvement projects of Automation and Controls systems for the Automated Equipment in a dynamic GMP regulated environment, requiring minimal downtime of the machinery. Responsibilities include fast response for troubleshooting to sustain machinery uptime when unscheduled downtime occurs, identification of improvements … conflicts and develop the necessary contingency plans to improve business continuity.Performs troubleshooting and modifications to the automated equipment adhering to Pharmaceutical and Medical Devices GMP change control standards and policies.Creates and modifies system specifications and standard operating procedures for the systems supported.Trains users and peers on systems.Supports software life cycle ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

safety standards in line with Greencore, customer, and legal requirements, with guidance from the QA Supervisor or Manager. Role Accountabilities • Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure • Apply an inquisitive audit mindset to identify root causes and reduce repeat … actions • Work safely at all times, promoting strong health, safety, and environmental standards What we're looking for • A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment • A proactive, detail-focused approach with a natural curiosity to challenge and improve standards • Confidence working hands ...

ensure maximum productivity. This position is under the direction of the Sanitation Supervisor. The Lead is responsible for following and enforcing all safety, GMP and SQF policies/procedures, as well as adherence to PPE/hygiene policies, in cooperation with the supervisor. The Lead is required to ensure that … shifts, cleaning and sanitizing tools and receptacles and other custodial functions as needed. Train new employees on standard operating procedures (safety, GMP AND SQF policies/procedures, PPE/hygiene policies) Coach all employees to follow Hello Fresh policies and procedures Support the production department by cleaning and preparing ...