1 to 14 of 14 GxP Jobs in the UK with Remote Work Options

heavily focused on quality, and experience in the pharmaceutical or medical industry is highly desirable. Key Responsibilities: Ensure successful client and regulatory audits of GxP activities across EMEA sites. Report and investigate quality and safety-related incidents and audits in a timely manner. Implement efficient, standardised systems and processes. Perform … Belgium, Switzerland, or Netherlands. Experience: Solid background in a quality or HSE role within the pharmaceutical or life sciences environment. Familiarity with a regulated GxP environment is essential. Qualifications: EU Quality or HSE qualification. ISO Lead Auditor qualification is desirable. Skills: Excellent communication, influencing, and facilitation skills. Ability to work more »

Pharmaceutical production or development environment, to include QC and working with staff on issues arising within a production environment. Familiar with the concepts of GxP systems and other pharmaceutical terms and acronyms. Experience of managing Tech transfers, troubleshooting and product development of product change projects including process, analytical, planning, documentation more »

other managers and staff and provide training, tools and techniques to enable others to achieve quality standard. Key Skills and Requirements: Significant understanding within GxP operational and quality roles. Operational experience in at least one of the following areas: Biostats, Data management, Clinical Trial Supply and Logistics, IRT, Pre-clinical more »

for CMC activities on drug substance, drug product both towards FDA and EMA is mandatory Solid experience with working in a regulated environment under GxP and with adherence to Company SOPs, policies and guidelines Updated knowledge of ICH GMP is required Excellent communication, presentation, and interpersonal skills. Self-driven and more »

supporting and improving business capabilities for Quality Systems within a regulated pharmaceutical environment . This role includes system ownership and service management for key GxP applications, such as Veeva Quality Vault (Document and Quality Management) and JazzLearn (the primary learning management system supporting GxP training). Essential Functions/Responsibilities … validation test protocols, such as IQ/OQ/PQ Collaborate with other System Owners, Jazz Digital QA and IS Compliance to ensure that GxP systems are operating as expected and are maintained in accordance with regulatory requirements and Jazz SOPs Work with IS Business Partners, Business Process Owners and … for a pharmaceutical company. Knowledge of Veeva Systems (advantageous) Knowledge of Learning Management Systems (particularly in the Pharma industry) Experience as System Owner for GxP systems Maintains knowledge of cGxP, IS Compliance, IS Security, SOX, data privacy & integrity, and other risk management considerations, and ensures they are embedded in projects more »

Delivery Consultant - GxP/MSP London - Liverpool Street £28K - £32K + Commission per placement i-Pharm Consulting is looking to hire a Delivery Consultant with a background in resourcing or delivery for key accounts. The Delivery Consultant will work within our GxP/Delivery Team sourcing Life Sciences professionals for more »

platform for Pharmaceutical and Biotech customers. This is groundbreaking work, reinventing the MES concept. So, as well as knowledge and experience of MES and GxP IT projects, you absolutely must be open to working in new ways with a flexible and creative mindset in tight collaborative teams with colleagues and … customers. Factorytalk has unique experience and know-how in creating, building, and validating GxP Apps using this modern digitalization tool. You will receive extensive training on Tulip, attain certification, and additional training on Factorytalk’s specialist App design, building, and validation methods to deliver Tulip solutions for GxP use. This more »

is heavily focused on quality, and experience in the pharmaceutical or medical industry is highly desirable.Key Responsibilities:Ensure successful client and regulatory audits of GxP activities across EMEA sites.Report and investigate quality and safety-related incidents and audits in a timely manner.Implement efficient, standardised systems and processes.Perform ad hoc assignments … Spain, Belgium, Switzerland, or Netherlands.Experience: Solid background in a quality or HSE role within the pharmaceutical or life sciences environment. Familiarity with a regulated GxP environment is essential.Qualifications: EU Quality or HSE qualification. ISO Lead Auditor qualification is desirable.Skills: Excellent communication, influencing, and facilitation skills. Ability to work across international more »

do business. The Opportunity Dechra Pharmaceuticals are looking for an experienced auditing professional to join our manufacturing division on a remote basis. Support the GxP and Regulatory compliance of Dechra Products by developing audit systems which will ensure process and product compliance with applicable GMPs/GDPs throughout the product … lifecycle. Develop, approve, and monitor the risk based GxP audit programme and budget for Dechra DPMS. Develop and support inspection readiness at Dechra Internal Manufacturing sites, sustaining their ability to successfully conclude regulatory inspections for Dechra's products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide … and review or preparation of responses to deficiencies) and on-site presence as required. Develop audit systems to ensure key elements of the Dechra GxP Quality Management System and the requirements of the product licences/marketing authorisations are effectively implemented throughout the internal and external manufacturing network (as required more »

We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who has previous regional experience with some auditing experience. The role is based from home and … for leading the output from a team of QSHE people based in the region. Key responsibilities and activities Successful client and regulatory audits of GxP activities across the EMEA sites. Timely reporting and investigation of quality and safety related incidents and audits. Added value to the business through implementing efficient … working on other Global Pharmaceutical accounts. The group is responsible for conduct of audits, training, and quality/safety investigations, all of which ensure GxP and SHE regulations are satisfied. This position is home based, however travel is expected within EMEA to visit the relevant client sites. Essential Solid grounding more »

PMDA and other global regulatory agencies. Who We Are Zigzag Associates partners with companies across the entire drug discovery and development process to improve GxP Quality against global regulatory standards. We are a global, certified woman owned company who put people first and forge lasting relationships to bring deep impact more »

in a fast-paced, agile-working environment Significant experience focusing on commercial country and product launches and being accountable Experience in the delivery of GxP projects and systems as several platforms will require GxP related changes and will be subject to Computer System Validation (CSV) Please call Edward Laing here more »

We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who has previous regional experience with some auditing experience. The role is based from home and … for leading the output from a team of QSHE people based in the region. Key responsibilities and activities • Successful client and regulatory audits of GxP activities across the EMEA sites. • Timely reporting and investigation of quality and safety related incidents and audits. • Added value to the business through implementing efficient … working on other Global Pharmaceutical accounts. The group is responsible for conduct of audits, training, and quality/safety investigations, all of which ensure GxP and SHE regulations are satisfied. • This position is home based, however travel is expected within EMEA to visit the relevant client sites. Essential • Solid grounding more »

re particularly keen to hear from those who have/are: Extensive Pharmaceutical Industry with hands on experience in development/quality in a GxP environment. Proven track record of implementing phase appropriate quality strategies Direct experience proving quality oversight of CDMOs Excellent working knowledge of FDA and EU GMPs more »