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Hyper Recruitment Solutions
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Validation Engineer

KentPermanent
£28,000 - £42,000 per annum
Job Reference: J5632205
Updated On: 17/09/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Contract Manufacturing Organisation

Skills: Chemistry - Analytical - Instrument Validation, Chemistry - Analytical - Development and Validation Analyst, Validation - Process Validation, Validation - Equipment Validation

Job Information

Role Overview

Hyper Recruitment Solutions are currently looking for a Validation Engineer to join a leading Pharmaceutical company based in the Kent area. As the Validation Engineer you will be responsible for providing technical and validation support for site engineering activities.

Key Duties and Responsibilities

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

1. You will be responsible for the development of detailed design specifications for new or modified Automated Process Control (APC)/ Equipment / Facilities / Utilities to satisfy user requirements.

2. You will generate and execute Design, Installation and operational Qualification protocols and reports in accordance with company policies and procedures. As the Validation Engineer you will provide input to the project plans detailing all validation activities and timings.

3. You will identify validation requirements for capital projects and modifications to existing validated APC, equipment, facilities and utilities in conjunction with the Validation Specialist / Site Validation Manager.

4. You will advise relevant user departments to ensure that implemented changes to production equipment / facilities are incorporated in to basic operating procedures.

Role Requirements


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

1. Relevant degree in a Chemical Engineering field.

2. Proven industry experience in validation of pharmaceutical equipment, facilities and utilities and control systems.

3. A working knowledge and practical experience with working to cGMP, MHRA / FDA regulatory requirements.


Key Words: Engineering / Validation / Equipment / Pharmaceutical / cGMP / APC / CDMO
Ben Walsh
Your Recruitment ConsultantBen WalshBen.Walsh@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.