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Computer Systems Validation Engineer

WiltshirePermanent
£40,000 - £50,000 per annum
Job Reference: J5634240
Updated On: 05/01/2021
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Software, IS&T

Skills: IS&T - Change Management, IS&T - Controls, IS&T - Systems Engineering, Quality Assurance - Compliance, Quality Assurance - Validation, Quality Assurance - CSV, IS&T - Data Integrity, IS&T - Testing

Job Information

Role Overview

We are currently looking for a Computer Systems Validation Engineer to join a leading pharmaceutical company based in the Wiltshire area. As the Computer Systems Validation Engineer you will be responsible for supporting?Computer Systems Validation (CSV)?activities regarding new and existing GxP systems supporting the site regulated business process

Key Duties and Responsibilities

Your duties as the Computer Systems Validation (CSV) Engineer your role will be varied however the key duties and responsibilities are as follows:

1. Your main focus as the CSV Engineer will be to support?Computer Systems Validation (CSV)?activities regarding new and existing GxP systems supporting the site regulated business process

2. You will provide specialized knowledge and information to guarantee the proper computerised system Life cycle from installation, to retirement ensuring the compliance with relevant regulatory requirements including FDA 21 CFR Parts 11 and 211 and EU GMP Annexes 11 and 15 and MHRA Guidance with a focus on the ER/ES compliance and DI principles.

3. You will be responsible for validation activities following a risk-based approach in accordance to GAMP 5 guide and the CS life cycle methodology are incorporated and documented appropriately for the systems in accordance with company standards and site procedures

4. You will work closely with all functions and in particular with project leaders, Engineering, IT, DI, QC and Quality

Role Requirements

To be successful in your application to this exciting opportunity as the Computer Systems Validation Engineer we are looking to identify the following on your profile and past history:

1. Good Knowledge of GAMP5 guide and MHRA ‘GXP Data Integrity Guidance and Definitions, FDA 21 CFR Part 11, EMEA Annex 11 regulations

2. Proven industry experience in Computer systems within the pharmaceutical industry

3. Experience with automation, computer and manufacturing systems especially in the sterile environment

Key Words: CSV, Computer System Validation, GXP, Data Integrity, GAMP5, Validation
David Powell
Your Recruitment ConsultantDavid Powelldavid.powell@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant 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 processionals and scientists. We look forward to helping you with your next career moves.