QA Batch Release Associate - Life Sciences - Liverpool
Our clientis a global biopharmaceutical company manufacturing plasma-derived, and recombination therapeutic products, who in turn deliver high-quality medicines that treat people with rare and serious diseases and we are now searching on an exclusive basis with the client to appoint aQA Batch Release Associate to join their busy and rewarding team on a contractual basis for a period of 12 months.
Responsibilities: Ensure that batch specific documentation and data, including batch release packs and lot release protocols, are reviewed and compiled for QA Manager/QP release. Ensure compliance with licensed and cGMP requirements, identification and resolution/escalation of issues that may impact batch release, and timely release of batches in order to meet strict supply demands. Ensure that other team objectives are achieved and to monitor this progress, suggest and support execution of required work, and suggest and implement improvements. Perform PTC /AE activities, as required, to ensure root cause investigations are completed in a timely manner and critical items are escalated to management. Assist with site quality systems, deviations, change controls, SOPs and self-inspections. Actively maintain and promote a cGMP compliant culture, ensuring the highest standards of Housekeeping and Safety are applied in the team, in accordance with current regulations and procedures
Requirements: Experience of working in a cGMP environment Experience of Quality Assurance systems, procedures and industry practices desirable A relevant degree
If this role is of interest to you, please apply now!
#LI-TE1 #J-18808-Ljbffr
Our clientis a global biopharmaceutical company manufacturing plasma-derived, and recombination therapeutic products, who in turn deliver high-quality medicines that treat people with rare and serious diseases and we are now searching on an exclusive basis with the client to appoint aQA Batch Release Associate to join their busy and rewarding team on a contractual basis for a period of 12 months.
Responsibilities: Ensure that batch specific documentation and data, including batch release packs and lot release protocols, are reviewed and compiled for QA Manager/QP release. Ensure compliance with licensed and cGMP requirements, identification and resolution/escalation of issues that may impact batch release, and timely release of batches in order to meet strict supply demands. Ensure that other team objectives are achieved and to monitor this progress, suggest and support execution of required work, and suggest and implement improvements. Perform PTC /AE activities, as required, to ensure root cause investigations are completed in a timely manner and critical items are escalated to management. Assist with site quality systems, deviations, change controls, SOPs and self-inspections. Actively maintain and promote a cGMP compliant culture, ensuring the highest standards of Housekeeping and Safety are applied in the team, in accordance with current regulations and procedures
Requirements: Experience of working in a cGMP environment Experience of Quality Assurance systems, procedures and industry practices desirable A relevant degree
If this role is of interest to you, please apply now!
#LI-TE1 #J-18808-Ljbffr
