Skills/education
~ BSc or equivalent experience – Life Science or QA discipline~2-4 years’ experience for QA Specialist 2 in pharmaceutical or CDMO industry in QA relevant roles~5-6 years’ experience for QA Specialist 3 in pharmaceutical or CDMO industry in QA relevant roles~ Document management experience”, “datePosted”: “2026-05-23”, “hiringOrganization”: { “@type”: “Organization”, “name”: “SRG”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__439465020__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “” } } }
Job title: QA Specialist 2/ QA Specialist 3 Location: Slough Contract Length: 5 months Working Hours: 37.5 hours/week Pay Rate: up to £19.66 / £25.55 p/h ( DOE) About the Role Working as part of QA system team, responsible for the implementation of global quality systems, including clean-up activities, on-site training, cross department communication, and preparation of initiatives. Additionally, overseeing the implementation and maintenance of global standards processes while supporting the management of documentation procedures. There are 2 vacancies available and candidates will be considered by experience level . Key Responsibilities Setting up and assisting in the implementation of new DMS and quality records global systems, including clean-up activities, preparation work, validation and qualification support, enrolment in the online training program, and alignment with stakeholders to ensure a robust system implementation. Provide regular updates on the project realization to line manager and/or Senior leadership team where required. Monitoring internal quality records to ensure timely completion, where applicable. Perform and support deviation or investigation where applicable Performing all business-related activities as reasonably requested and instructed by the line manager or senior management team. Taking personal responsibility for fostering a strong quality culture.
Skills/education
~ BSc or equivalent experience – Life Science or QA discipline~2-4 years’ experience for QA Specialist 2 in pharmaceutical or CDMO industry in QA relevant roles~5-6 years’ experience for QA Specialist 3 in pharmaceutical or CDMO industry in QA relevant roles~ Document management experience…
