CSV Specialist responsible for site validation life cycle of computerised systems.
Are you a CSV Specialist professional with pharmaceutical experience? An opportunity has arisen for a CSV Specialist to join a team in North London - on a permanent basis.
About the organisation:
You will be working for an organisation that specialises in the development of pharmaceutical products.
About the Job:
As CSV Specialist you will take ownership of onsite validation of computerised systems. You will be responsible for both automated and IT systems.
You will be the site subject matter expert for CSV. You will provide support and ensure compliance of system specification, design, testing and decommissioning.
The role is permanent and comes with good benefits.
- You will have a degree (or equivalent) in Engineering, Science or similar.
- You will have significant validation experience within a pharmaceutical or biopharmaceutical manufacturing area. (API/Fill finish)
- You will have good understanding of GAMP5 and GMP
- You will have a sound understanding of pharmaceutical technology and have previously helped teams build a compliant CSV base.
How to apply:
Apply now via the SRG website.
If this role is not quite right for you, but might be for somebody in your network - please forward this onto them. SRG pay a referral fee for any successful candidates.
Loz Mitchell - Pharma
0161 868 2215
your application has been submitted
Back to job search