Working within a small team, the Validation Engineer role will primarily involve preparing and executing validation/ qualification protocols.
Inizio Engage have the pleasure of working with one of the fastest growing privately owned businesses in the UK involved in the development, manufacture and testing of pharmaceutical and biotechnology products and medical devices.
The ideal candidate will have a good understanding of manufacturing practice and background knowledge of clean rooms but our Client will also consider new to industry candidates with a science degree for this role.
Testing of gel electrophoresis products according to pre-assigned testing and validation protocols, identifying and investigating any detrimental trends via good attention to detail and root cause analysis.
General
They are seeking a dynamic individual to undertake validation activities relating to gel electrophoresis product development in a timely and efficient manner as directed by the New Product Development Manager and with reference to the appropriate procedures / guidelines.
Opportunity to work for a leading and well established medical diagnostic company.
Experience needed: Experience of working in manufacturing engineering or process engineering within a complex engineering or manufacturing environment such as defence, aerospace, automotive, robotics and similar.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a Senior QC Analyst to join the QC Technical Services Team on a contract basis.
This opportunity is for a QC Analytical Validation Specialist to join the QC Technical Services Team on a contract basis.
The duration of the contract will be 23 months.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.