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CSV Validation Specialist

WiltshirePermanent
£40,000 - £45,000 per annum
Job Reference: J5632697
Updated On: 28/01/2020
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical

Skills: Engineering - Validation Perm, Quality Assurance - GMP, Quality Assurance - Validation, Quality Assurance - CSV, Validation - Process Validation, Validation - Equipment Validation, Validation - Cleaning Validation, Validation - Facilities/Utilities Validation

Job Information

Role Overview

We are currently looking for a CSV Validation Specialist to join a leading pharmaceutical company based in the Wiltshire area. As the CSV Validation Specialist you will be responsible for or performing qualification, validation and engineering activities in a GxP (GMP / GLP) environment.

Key Duties and Responsibilities

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

1. As the CSV Validation Specialist you will be performing your activities in a GxP environment in close contact with QC, Engineering, Production and QA.

2. The CSV Validation Specialist will write, review and finalize validation documentation for new and existing lab equipment and computerised systems in the GxP environment.

3. As the CSV Validation Specialist you will optimize and maintain operational procedures in validation, calibration and the life cycle of systems based on regulations and guidance documents.

4. The CSV Validation Specialist will interact with internal and external suppliers in function of design, validation, implementation, maintenance and calibration of systems.

Role Requirements

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

1. Relevant degree in a relevant field of sciences.

2. Proven industry experience in Validation in the Pharmaceutical Industry.

3. A working knowledge and practical experience with Validation in a Pharmaceutical Environment


Key Words: Validation Specialist / Validation Engineer / Validation / IQ / OQ / PQ / GMP / MHRA / HVAC / Biologic / Manufacturing / FDA / Serialisation / Laboratory Systems / Control Systems / Pharmaceutical / cGMP / Computer Systems / CSV / GxP / CSV Validation Specialist / LIMS
Jack Turnell
Your Recruitment ConsultantJack Turnelljack.turnell@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.