101 to 115 of 115 GMP Jobs

ensure the delivery of safe and legal cannabis. Curaleaf International’s network includes a clinic, pharmacy, and laboratory in the UK; cultivation and EU-GMP processing facilities in Portugal; an EU-GMP processing, quality assurance and research site in Spain; Four20 Pharma wholesaler and distributor in Germany; a Polish wholesaler … clinic; and the EU-GMP producer Northern Green Canada. Curaleaf International is part of Curaleaf Holdings, Inc., a leading international producer and distributor of consumer cannabis products. Our Values: Our Values: Lead & Inspire, Commit to Win, Driven to Deliver Excellence, Customer Obsession, One Curaleaf Equal opportunity Curaleaf International ...

require someone with direct hands-on experience and expertise in any of the following: Working in a regulated lab environment such as GLP, GMP, and with EPA/FDA GLP or GMP method validation and product characterization. Responsibility for analytical instrument method development, maintenance, supplies, repairs, purchases, and analyses ...

architectures supporting business- critical production systems. Develop target-state architectures and migration strategies for large-scale technology modernisation initiatives. Ensure solutions comply with GMP/GxP requirements, validation standards, cybersecurity frameworks, and industry best practices. Experience required Extensive experience as a Solutions Architect, Enterprise Architect, or Technical Architect within regulated … environments, including industrial systems, plant infrastructure, and manufacturing technology. Proven experience delivering complex IT infrastructure transformation and migration programmes. Significant cybersecurity experience within GMP/GxP-regulated environments. #J-18808-Ljbffr ...

function, support and develop the QA team, and make sure products meet customer, legal and internal quality standards. You'll also be involved in GMP, audits, quality control, continuous improvement and working closely with Production to resolve quality issues. As QA Team Leader, you'll work closely with the Operational … quality concerns are identified and reported promptly. Carry out additional quality assessments, including dry matter and hot box testing, where required. Manage the site GMP audit system and participate in internal auditing activities. Support preparation for internal and external audits. Assist with recording and monitoring weekly quality KPIs. Support ...

choose the right tooling Experience in a highly regulated manufacturing environment. Medical device or ISO 13485 experience is a plus. Working knowledge of GMP Strong GD&T, blueprint reading, and knowledge of sampling and inspection plans Comfort with precision measuring instruments Proficiency with AutoCAD, SolidWorks, MS Office, and production … choose the right tooling Experience in a highly regulated manufacturing environment. Medical device or ISO 13485 experience is a plus. Working knowledge of GMP Strong GD&T, blueprint reading, and knowledge of sampling and inspection plans Comfort with precision measuring instruments Proficiency with AutoCAD, SolidWorks, MS Office, and production ...

ours in Milton Keynes. The Ideal candidate would be proactive, detail-oriented and comfortable working in a fast-paced manufacturing environment. Key Responsibilities: - GMP and hygiene audits. Production start-up checks. Product quality assessments and taste panels. Allergen verification and environmental monitoring activities. Completion and review of quality documentation. Supporting … food safety standards. Requirements: - Previous experience in a food manufacturing environment, ideally within Quality Assurance, Quality Control, or Food Safety. Good understanding of GMP, hygiene standards, allergen control, and food safety requirements. Experience completing factory inspections, quality checks, product assessments, and documentation would be beneficial. Confident using Microsoft Office applications ...

computer systems, processing warehouse transactions, writing professional emails, organising documentation and ensuring stock and warehouse records are accurate. Pharmaceutical experience would be preferred, especially GMP or GDP knowledge, but this is not essential. Strong SAP, ERP, warehouse administration and computer skills are the key requirements. The Role As a Warehouse … emails and communicating clearly with internal and external contacts Maintaining high levels of accuracy, organisation and traceability across warehouse documentation Working in line with GMP, GDP and pharmaceutical compliance standards where required What Were Looking For We are looking for candidates who: Have previous experience in warehouse administration, logistics, distribution ...

context switching between multiple projects and on-call responsibilities Preferred Qualifications Experience managing open source projects Prior experience with SOC2/ISO 27001/GMP/CFR Part 11 Prior experience at a hardware startup or robotics company Familiarity with biomanufacturing or lab automation Experience working in regulated environments (e.g. … GMP, FDA, ISO standards) Physical & Working Conditions Standard work schedule with occasional evenings, weekends, or on-call support for critical issues or time-sensitive maintenance Perks & Benefits Total Rewards & Life at Multiply Labs Competitive Compensation: Salary range of $175,000 - $230,000 plus meaningful early-stage equity. We want ...

Sharp Services, LLC seeks a Computerised Systems Validation Specialist to oversee CSV status of GMP IT systems at the Rhymney site, with onsite or hybrid working and travel to European sites. You will maintain validation master plans, prepare documentation, and coordinate validation activities with IT, Operations, Supply Chain and QA. … role requires GMP knowledge, experience in pharma environments, and the ability to travel regularly to Sharp sites in Belgium and the Netherlands. #J-18808-Ljbffr ...

Contract. Job Purpose The Temporary QA Document Control Associate supports the Quality Assurance (QA) department by assisting with the digitization, organization, and verification of GMP documentation. This position is responsible for scanning controlled documents and ensuring that electronic records are complete, legible, and are an accurate representation of the original … data integrity and document accuracy. Principal Accountabilities Ensure compliance with all relevant laws and regulations as well as company procedures, policies, and SOPs. Scan GMP documentation using approved/appropriate document scanning procedures. Verify that scanned electronic documents are complete, legible, and accurately represent the original paper documents and compliant ...

critical production systems. The role is remote with an initial 6-month contract for a high-impact life sciences programme, requiring extensive experience in GMP/GxP and cybersecurity within #J-18808-Ljbffr ...

stopped, as the ozone may bleach the fish if loading speed is not maintained. Maintain tidy work environment. Comply with all facility GMP rules and policies and all processes and requirements of the Food Safety and Quality Management System as applicable. Complete other tasks at request of Medium Care Supervisor. … Requirements: Preferred Qualifications Previous experience in food manufacturing or food production. Knowledge of Good Manufacturing Practices (GMP), HACCP, and food safety practices. Previous experience working with seafood, salmon, or other food products. Previous experience in food packaging or on production lines. Ability to work effectively in a fast-paced production ...

play a key role in data preparation in advance of transactions (e.g. buy‐ins); 2) conduct data audits, benefit audits and calculations; 3) undertake GMP projects. For this reason, prior GMP experience is essential. You will also have a good understanding of the technical aspects of defined benefit pensions, with ...

dedicated Quality Analyst to support the digital transformation journey of a manufacturing site, focusing on implementing and maintaining IT systems that align with GMP regulations. This role will primarily involve working with Quality Systems such as LIMS, CDS, and other QC equipment applications, while also supporting broader manufacturing IT needs. ...

into delivery, processes and capability Own commercial performance, identifying growth opportunities and supporting pitches Provide technical leadership across analytics, tagging, MMM, BI and GMP Lead and develop a senior leadership/practitioner team, with responsibility for a large wider function Represent the data practice with C-suite clients and senior … multiple data/marketing disciplines Agency experience preferred, particularly within the media/marketing ecosystem Technical credibility across analytics, BI, MMM and/or GMP - you don't need to be hands-on day-to-day, but must be able to challenge and guide technical teams A strong commercial track ...