Computer Systems Validation Consultant

Our client is an exciting and innovative start-up company, developing ground breaking technology, using Blockchain and AI software solutions for the Pharmaceutical / Healthcare sector. Currently looking for a CSV Contractor/Consultant to join the company based in the Essex area. You will be responsible for a number of projects requiring validation work in a GMP environment.

Duties & Responsibilities -

Your duties as the CSV Contractor will be varied however the key duties and responsibilities are as follows:

1. As the CSV Contractor, you will be responsible for validating various computer systems which will include a variety of ERP based systems and Laboratory systems within a GMP environment.

2. Your role as the CSV Contractor will be to work on projects that include networking standalone systems, and the addition of new instruments to ensure that they are compliant to GAMP5 and regulatory guidelines.

3. You will have significant experience across CSV within the pharmaceutical industry. This will be across both Laboratory and ERP systems.

4. You will utilise your experience and knowledge of GAMP5 regulations, Annex 11 and CFR Part 11 to ensure that computer systems are validated in a timely manner.

Role Requirements -

To be successful in your application for this exciting opportunity as the CSV Contractor our client is looking to identify the following on your profile and past history:

1. Relevant degree in a Scientific or Technical discipline.

2. Proven industry experience in a CSV role within the pharmaceutical industry.

3. A working knowledge and practical experience with CSV for laboratory and ERP systems as well as required compliance within the pharmaceutical industry.