26 to 43 of 43 GxP Jobs

solver who can work through complex issues • Good attention to detail • Experience of working with databases and computer systems • Experience of working in a GxP environment, experience of Computer Systems Validation Interested? Apply now for immediate consideration or contact Elias Adem on eadem@planet-pharma.co.uk We are an equal opportunities more »

play a pivotal role in connecting the business needs for designated process areas with requirements of both formal and informal learning in a regulated GxP environment. You will Connect with stakeholders of all levels of seniority to ensure a fully inclusive, sustainable learning solution is created to support the long more »

validating computer systems in a Biopharmaceutical setting. A Degree (or equivalent experience) in a Science or related discipline . Experience in the validation of GxP software and Laboratory systems. Prior ERP integration experience would be advantageous, but not essential. more »

and small projects. Provide support to other team members in accordance with experience and competencies. To ensure documentation required for statutory, H&S and GxP standards are completed and filed. Arrange contractor site inductions and enabling work to start safely. Propose ideas/initiatives for continuous Improvement to streamline, increase more »

business users, establish and maintain a positive professional relationship with users and clients Participate in testing, documentation and implementation of assigned projects Execution of GxP-related activities in adherence to standard operating procedures Additional duties as and when required, travel to other sites as required Essential Skills: Desktop operation and more »

business users, establish and maintain a positive professional relationship with users and clients Participate in testing, documentation and implementation of assigned projects Execution of GxP-related activities in adherence to standard operating procedures Additional duties as and when required, travel to other sites as required Essential Skills: Desktop operation and more »

Manage, coach and mentor more junior members of staff. Provide clear scientific and technological leadership to direct reports. Comply with all relevant safety and GxP procedures. Plan and prioritise own, and team’s work with input from senior manager when required. Involve in CRO’s selection process. Provide an oversight more »

be a part of these roles. Good understanding/knowledge of software engineering (should come with above) Designing strategy and setting strategy Knowledge of GxP procedures and familiarity with ISO9001/ISO27001 Technologies they use: Frontend, React or python. Backend is Golang. If you're interested in working for a more »

Quality Business Analyst BA in charge of being the link with business stakeholders and the Quality/BA Team. Experience as a BA - circa 5+ years to work independently. Experience with Veeva and other quality systems. Must understand GXP. Order 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 »

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 »

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 »

join the Digital Organization reporting to the Director of Digital Lab Systems. The engineer will be responsible for implementing and supporting IT systems in GXP Lab and Manufacturing sites. The Engineer will collaborate with the digital team to develop effective approach to integrate IT architecture into the labs. The Engineer … with automation engineers, plant engineers, lab engineers, scientists, and operations teams to design, develop, and support the lab IT systems. As this is a GXP environment, the candidate must be familiar with the GXP process and the IQ/OQ/PQ Validation process for IT systems. In addition, the … IR35 contract and is onsite 5x a week Must Haves: Proven experience working in IT Infrastructure in manufacturing and lab systems Familiar with the GXP process and the IQ/OQ/PQ Validation process for IT systems. Experience with implementing IT Applications and troubleshooting IT applications Degree in Computer 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 »

leading continuous improvement of quality and regulatory systems. The role will support and ensure that the site and related functions are in compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The … tracking of site compliance commitments and follow up actions. Coordinate and support the delivery of Quality Compliance Metrics/KPIs to key stakeholders. Identify GxP trends and communicate these to relevant stakeholders. Support compliance risk management activities and implementation of risk mitigation plans. Working with the wider site functions to … procedures according to internal guidelines and UK/EU/US/ICH and other region specific guidance. Lead Quality Management Review meetings highlighting GxP areas of concern and working to support and track actions that are to be taken. Support quality related investigations, assist in the development and approval more »

Piramal Grangemouth and maintenance of Regulatory Registrations/Licenses/Certifications. The role will support the site and related functions in maintaining compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The … documentation according to internal guidelines and UK/EU/US/ICH and other region specific guidance. •Lead Quality Management Review meetings highlighting GxP areas of concern and working to support and track actions that are to be taken. •Support quality related investigations, assist in the development and approval more »

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 »

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 »