Hyper Recruitment Solutions
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Cleaning Validation Engineer

United KingdomContract
£40 - £60 per day
Job Reference: J5631482
Updated On: 14/05/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Biotechnology, Bioprocessing

Skills: Validation - Process Validation, Validation - Cleaning Validation

Job Information

Role Overview

We are currently looking for a Cleaning Validation Engineer to join a leading Biopharmaceutical company based in the UK.

As the Cleaning Validation Engineer you will be responsible for both hands on Cleaning Validation activities and problem solving / creating a Cleaning Validation strategy within a Sterile environment working with Biological pharmaceutical products.

Key Duties and Responsibilities

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

1. Provide Cleaning Validation expertise and understanding working with sterile biological products and formulations in a GMP pharmaceutical environment working with aseptic processes.

2. As the Cleaning Validation Engineer you will contribute to Cleaning cycle Development and Verification, and Cleaning Validation Protocols. This may include parameter selection, determining order of operations, troubleshooting, sampling, and data analysis.

3. You role as the Cleaning Validation Engineer will be to plan and help to execute the Validation strategy for CIP systems to ensure cleaning of product contact surfaces.

4. You will bring your Cleaning Validation experience and initiative / problem solving skills to a fast paced pharmaceutical environment in order to offer different solutions and potentially change Validation Processes.

Role Requirements

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

1. Relevant degree or qualification in a Scientific or Engineering discipline

2. Proven Cleaning Validation experience within the pharmaceutical industry.

3. A working knowledge and practical experience with Cleaning Validation in a sterile, aseptic and biological GMP environment is beneficial.


Key Words: Cleaning Validation / Sterile / GMP / Pharmaceutical / Validation / CIP / Validation Master Plan / Qualification / Process Validation / Equipment Validation / Validation Engineer / Biopharmaceutical
Georgia St John-Smith
Your Recruitment ConsultantGeorgia St John-SmithGeorgia.smith@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.