Entrust Resource Solutions Group - Validation Engineer (Contractor)
Job Title:
Validation Engineer (Contractor) Category:
Technical roles Closing Date:
28/02/2025 VALIDATION ENGINEER (CONTRACT ROLE) 12 - 18 MONTH CONTRACT CENTRAL SCOTLAND Are you a meticulous professional with a passion for precision and quality? A leading organisation in Central Scotland is seeking a dedicated Validation Engineer for a 12-month contract role, driven by recent and future expansion. This is an exceptional chance to contribute to a dynamic team, ensuring the highest standards in product and process validation. Imagine working in a stimulating environment where your expertise is valued and your contributions make a tangible impact. Responsibilities: Support the validation of equipment, processes, and systems to ensure compliance with industry standards and regulatory requirements. Develop and execute validation protocols. Conduct risk assessments. Maintain detailed documentation. Minimum Requirements: Degree in Engineering, Life Sciences, or a related field. Substantial experience in validation within a regulated industry, such as pharmaceuticals, biotechnology, or medical devices. Proficiency in validation methodologies, including IQ, OQ, and PQ. Strong analytical skills and the ability to troubleshoot complex issues. Thorough understanding of GMP regulations. Experience in Aseptic processing is very desirable. Skills: Excellent communication skills, both written and verbal. Ability to work effectively within a team. Methodical mindset with a proactive attitude. To find out more about this opportunity, please contact Lynsey today on 07712412095 or send an up to date copy of your CV to Lynsey@entrustrs.com
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Job Title:
Validation Engineer (Contractor) Category:
Technical roles Closing Date:
28/02/2025 VALIDATION ENGINEER (CONTRACT ROLE) 12 - 18 MONTH CONTRACT CENTRAL SCOTLAND Are you a meticulous professional with a passion for precision and quality? A leading organisation in Central Scotland is seeking a dedicated Validation Engineer for a 12-month contract role, driven by recent and future expansion. This is an exceptional chance to contribute to a dynamic team, ensuring the highest standards in product and process validation. Imagine working in a stimulating environment where your expertise is valued and your contributions make a tangible impact. Responsibilities: Support the validation of equipment, processes, and systems to ensure compliance with industry standards and regulatory requirements. Develop and execute validation protocols. Conduct risk assessments. Maintain detailed documentation. Minimum Requirements: Degree in Engineering, Life Sciences, or a related field. Substantial experience in validation within a regulated industry, such as pharmaceuticals, biotechnology, or medical devices. Proficiency in validation methodologies, including IQ, OQ, and PQ. Strong analytical skills and the ability to troubleshoot complex issues. Thorough understanding of GMP regulations. Experience in Aseptic processing is very desirable. Skills: Excellent communication skills, both written and verbal. Ability to work effectively within a team. Methodical mindset with a proactive attitude. To find out more about this opportunity, please contact Lynsey today on 07712412095 or send an up to date copy of your CV to Lynsey@entrustrs.com
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