Get new jobs by email
- ...newly assembled team and help contribute towards the development of their site. Responsibilities Serve as the point of contact for quality at both the site level and with external inputs, coordinating and attending Quality working group meetings. As QA specialist,...SuggestedContract workFlexible hours
- ...Quality Assurance Specialist - Ireland, Sligo - 12 Month Contract Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for aQuality Assurance Specialist to join their state-of-the-art pharmaceutical facility. They have invested $...SuggestedContract work
- ...Our Client , a leader in the Pharmaceutical Industry is seeking a Quality Assurance Specialist/QP to join their team i n their Sligo facility | 12 month contract. Responsibilities: · Comply with EudraLex Volume 4 EU Guidelines for Good Manufacturing Practice for...SuggestedContract work
£87.1k - £104.6k per annum
...Manufacturing Practice (GMP) for products manufactured * Ensure that products are manufactured in accordance with the relevant GMPs. * The Quality Assurance Specialist / Qualified Person (QP) is responsible for the disposition of bulk product manufactured at site as acceptable...SuggestedContract work- ...Quality Operations Compliance Specialist - Ireland, Sligo - 12 Months Contract Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for aQuality Operations Compliance Specialist to join their state-of-the-art pharmaceutical facility...SuggestedContract work
- ...documents are maintained to support technology transfers and new product introduction project timelines. * Ensure application of Quality Risk Management principles as applicable. * Act as the QA in QA activities in project work-streams involving cross-functional, multidepartment...SuggestedContract work
- ...onsite role offering the opportunity to work in a collaborative and dynamic environment. The successful candidate will play a key role in Quality Assurance activities supporting the qualification and validation of manufacturing operations, while ensuring compliance with GMP and...SuggestedPermanent employmentFull time