- 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
- 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
…