overall group objectives and development of staff. Ensure that own work, and that of the team, complies with GMP, Good Documentation Practice (GDP) and GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g., SOP's, Protocols, etc). Requirements Experience working in a Pharmaceutical/ more »
a track record in Leading the HSE function across multiple companies in a Pharmaceutical environment. It is key that you have experience within a GXP/GMP environment. Purpose of the Job Health, Safety & Environment Lead and provide oversight and Global strategic leadership covering health, safety, and environment across the more »
opportunity to go permanent) Our client a Biotechnology Research company are currently hiring for a Labware Developer who has preferably worked in a GCP, GXP environment. Requirements; Experience with LIMS SQL Skills Understand Lab Processes The client are looking to hold interview ASAP, please apply if this role would be more »
serve as a consultant to the Clinical Development teams, providing guidance on GCP activities related to quality. Primary Responsibilities: Defining, maintaining, and monitoring the GxP Quality Management System (QMS). Making sure the QMS meets all the necessary regulatory requirements, with a strong focus on GCP compliance. Supporting and guiding … the Clinical Development teams in defining compliant procedures within GxP functions and effectively managing quality issues. Handpicking and documenting responsibilities for external contracted organizations that support the GxP activities. Keeping a close eye on the performance of the GxP service providers to ensure they meet the relevant quality standards. Taking more »
City of London, London, United Kingdom Hybrid / WFH Options
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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 »
Business Administrator for Veeva eQMS, oversee quality associated records and ensure these activities conform to regulatory requirements. Manage the controlled document scheme, act as GxP archivist, and deliver QA training activities. duties within Quality function. It is desirable, but not essential for the candidate to have a comprehension of basic … reports and dashboards in Veeva. Provide eQMS training to ensure competence across the business and maintain associated controlled documents. Ensure the appropriate storage of GxP documentation. Act as the primary company archivist by coordinating and preparing documentation for the offsite archive. Ensure appropriate process in place for the recall of … documents when requested. Administration of the quality assurance logs such as signature, notifications, QTA and audits. Document owner for GxP documents such as policies and the quality manual. Manage the controlled document scheme, including issuance and reconciliation. Provide information for Batch Record Review, QP certifications, Sponsor Release as and when more »
