I'm currently looking for a CSV Specialist to join a leading product development business based in the Glasgow area. This is a fantastic opportunity to be able to work across multiple different projects across various different pharmaceutical and biological areas. As the CSV Specialist, you will be responsible for the following:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CSV Specialist will be varied, however the key duties and responsibilities are as follows:
1.Identify and document computer systems that impact GxP requirements, helping with the performance of the validation of identified systems across the facility.
2.Validation of a brand new tablet filling line for the facility, including the qualification of the SCADA, MES, Dashboarding and Scheduling systems.
3.Action the CSV schedule to ensure all quality, manufacturing and engineering systems remain to GxP and GAMP5 requirements.
4.Support others in the generation of the lifecycle CSV deliverables for each computer system, including validation plans and risk assessments.
To be successful in your application to this exciting opportunity as the CSV Specialist we are looking to identify the following on your profile and history:
1.Educated to degree level, either within Pharmaceutical, IT or Life Science subjects.
2. Proven industry experience working on practical CSV and Validation projects.
3. A working knowledge and practical experience of significant CSV experience, operating within a GMP environment.
Key Words: CSV, Validation, Computer Systems Validation, GMP, GAMP5, GxP, SCADA
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.