Smart4 Sciences are currently working with a Pharmaceutical Company in North Wales to recruit a QA Officer to... Read more
Smart4 Sciences are currently working with a Pharmaceutical Company in North Wales to recruit a QA Officer to join a small team responsible for all aspects of GDP and GMP compliance.
This QA Officer position is a brilliant opportunity for candidates with 1+ years GDP/GMP experience to further their career within QA with a company who can provide strong progression opportunities
Key Responsibilities
Respond to and action quality enquiries and quality management activities including deviations, change controls, risk assessments, complaints etc.Support internal and external GDP/GMP auditsAuthor, review and archive quality documentation including SOPs, PQRs, supplier agreementsEnsure GMP/GDP compliance at all timesKey Requirements
Prior GDP/GMP experience within the pharmaceutical/medical device industries is essentialPrior experience working with Pharmaceutical Quality Management Systems is essentialA pro-active, can do attitude is essentialInterviews for this QA Officer position are imminent so please apply now or contact Gareth Gooley at Smart4 Sciences for more information.
Read lessSmart4 Sciences - QA Manager/RP/RPi - London - hybrid positionSmart4 Sciences are currently partnered with a Global Biopharmaceutical... Read more
Smart4 Sciences - QA Manager/RP/RPi - London - hybrid position
Smart4 Sciences are currently partnered with a Global Biopharmaceutical company looking to recruit a QA Manager/RP/RPi to join their team on a hybrid basis at their UK Head Office in London.
As a QA Manager/RP/RPi you will responsible for the upkeep of the QDA wholesale licence for the company, working closely with CMOs across the EU on supplier quality incidents and releasing finished product in line with RP/RPi requirements.
Key Requirements.
RPi certification with experience operating on and managing a WDA LicenceA strong background in all aspects of GMP/GDP Quality Assurance within the Pharmaceutical/Biopharmaceutical industryA strong background in supplier quality, managing CMOs, audits, inspections etcIf this role sounds of interest please apply today or contact Gareth Gooley at Smart4 Sciences for more information
Read lessSmart4Sciences are currently working with a global analytical research and testing provider to recruit a Quality Manager GMP... Read more
Smart4Sciences are currently working with a global analytical research and testing provider to recruit a Quality Manager GMP their MHRA, FDA AND UKAS regulated facility in Kent.
As a Quality Manager you will be a key part of the site leadership team and responsible for all QA functions including processes, systems and staff - liaising with other Quality Managers across the group to ensure a unified approach to quality across all global sites.
Key responsibilities
Oversee the site QA function, ensuring compliance with GMP, ISO 17025, FDA 21 CFR 820, and other regulatory standards.Lead a team of Quality Specialists, promoting a positive culture of quality compliance and upskilling staff members through regular coaching/trainingLead investigations, audits, non-conformances, and supplier quality to drive continuous improvementKey Requirements
Significant experience in GMP Quality Assurance from the Pharmaceutical and/or Medical Device industries including management and leading of teamsA demonstrable background in continuous improvement with a proficiency in Six Sigma and Lean MethodologiesPrior experience in a CRO/CDMO environment with the ability to manage multiple priorities in busy project based environments.Interviews for this Quality Manager position are imminent so please apply today or contact Gareth Gooley at Smart4Sciences for more information
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