1 to 10 of 10 GxP Jobs with Remote Work Options

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 »

with a focus on FDA & EMA regulations Excellent interpersonal, verbal, and written communication skills with the ability to diplomatically address quality issues Experience with GXP QA systems, processes, and procedures such as documentation and record management, change control, deviations, investigations, training, and CAPA Bachelor s degree in a scientific discipline 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 »

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 »

be beneficial to your application, but is not essential: Bachelors degree (or equivalent) in a scientific or technical discipline Worked within a pharmaceutical/GxP environment in a Quality related role Familiarity with the production of solid dose oral products Management of electronic & physical documentation systems Reward For the successful more »

awareness program (SETA) across all business functions. Manage external resources supporting the security awareness activities. Desirable Experience: Implementing controls and managing compliance risks regarding GXP regulated systems, data protection regulations such as EU and UK GDPR, CCPA, and cybersecurity regulations such as the EU NIS2 and USA SEC Disclosure Requirements. more »

Laboratory Information Management Systems, and are keen to develop their skills in an Information Technology environment. Knowledge of the different Pathology disciplines Knowledge of GxP regulations and system validation The ability to speak Welsh is desirable for this post; Welsh and/or English speakers are equally welcome to apply. 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 »

support in a team responsible for the delivery of the scientific and technical activities of the Immunoassay Group (IAG) and other groups within the GxP test facility when required. This post sits within the IAG Team. The successful candidate would be educated in degree level in a relevant subject area … of the application of serological assays to support clinical trials and/or product characterisation would be an advantage. Experience of working within a GXP environment is highly desirable. This post is not suitable for biomedical scientist accreditation. About us We pride ourselves as being an employer of choice, where more »