Validation Engineer

We are currently looking for a Validation Officer to join a leading pharmaceutical company based in the East Sussex area. As the Validation Officer, you will be responsible for ensuring that all processes, equipment, cleaning methodologies, utilities/facilities, computer systems, and analytical methods are validated. Effectively managing and executing...

We are currently looking for a Validation Officer to join a leading pharmaceutical company based in the East Sussex area. As the Validation Officer, you will be responsible for ensuring that all processes, equipment, cleaning methodologies, utilities/facilities, computer systems, and analytical methods are validated. KEY DUTIES AND RESPONSIBILITIES: Your...

Process Engineer / Validation Engineer, Medical Device Location: Coventry Type: Permanent role Hours: Monday to Friday (days), flexible hours & potential for early finish on a Friday Salary: Very competitive (open to discussion on this) Additional: 25+ BH holidays, income protection, life insurance, enhanced pension scheme Our client, a global medical...

About the RoleWe are seeking a highly experienced Senior Manufacturing Engineer to lead our global standards and validation efforts at CHEP. As a key member of our engineering team, you will be responsible for establishing and maintaining manufacturing standards, validation processes, and documentation practices across our global operations.Key...

Key Responsibilities: Requirements : Experienced Verification Engineer with:  Minimum of 5+ years of relevant experience at IP level verification  Expertise in verification languages in particular SV and UVM methodology  Available to work on long-term contract (at least one year)  A good listener who will gain a clear knowledge of what is...

Key Responsibilities: Requirements : Experienced Verification Engineer with:  Minimum of 5+ years of relevant experience at IP level verification  Expertise in verification languages in particular SV and UVM methodology  Available to work on long-term contract (at least one year)  A good listener who will gain a clear knowledge of what is...

Key Responsibilities: Requirements : Experienced Verification Engineer with:  Minimum of 5+ years of relevant experience at IP level verification  Expertise in verification languages in particular SV and UVM methodology  Available to work on long-term contract (at least one year)  A good listener who will gain a clear knowledge of what is...

Key Responsibilities: Requirements : Experienced Verification Engineer with:  Minimum of 5+ years of relevant experience at IP level verification  Expertise in verification languages in particular SV and UVM methodology  Available to work on long-term contract (at least one year)  A good listener who will gain a clear knowledge of what is...

Key Responsibilities: Requirements : Experienced Verification Engineer with:  Minimum of 5+ years of relevant experience at IP level verification  Expertise in verification languages in particular SV and UVM methodology  Available to work on long-term contract (at least one year)  A good listener who will gain a clear knowledge of what is...

Process Engineer / Validation Engineer, Medical Device Type: Permanent role Hours: Monday to Friday (days), flexible hours & potential for early finish on a Friday Additional: 25+ BH holidays, income protection, life insurance, enhanced pension scheme Our client, a global medical devices company, is looking to appoint a Process Engineer (PE) to work at...

Key Responsibilities: Have you got what it takes to succeed The following information should be read carefully by all candidates.Requirements : Experienced Verification Engineer with:  Minimum of 5+ years of relevant experience at IP level verification  Expertise in verification languages in particular SV and UVM methodology  Available to work on...

Key Responsibilities: Requirements : Experienced Verification Engineer with:  Minimum of 5+ years of relevant experience at IP level verification  Expertise in verification languages in particular SV and UVM methodology  Available to work on long-term contract (at least one year)  A good listener who will gain a clear knowledge of what is...

Job Summary:Calibre Scientific is seeking a highly skilled Regulatory Validation Specialist to join our team. As a key member of our environmental validation services team, you will be responsible for conducting testing and inspection at client sites, troubleshooting, and repairing systems as necessary, and preparing accurate reports and documentation of...

Job Summary:Calibre Scientific is seeking a highly skilled Regulatory Validation Specialist to join our team. As a key member of our environmental validation services team, you will be responsible for conducting testing and inspection at client sites, troubleshooting, and repairing systems as necessary, and preparing accurate reports and documentation of...

Job Summary:Calibre Scientific is seeking a highly skilled Regulatory Validation Specialist to join our team. As a key member of our environmental validation services team, you will be responsible for conducting testing and inspection at client sites, troubleshooting, and repairing systems as necessary, and preparing accurate reports and documentation of...

Job Summary:Calibre Scientific is seeking a highly skilled Regulatory Validation Specialist to join our team. As a key member of our environmental validation services team, you will be responsible for conducting testing and inspection at client sites, troubleshooting, and repairing systems as necessary, and preparing accurate reports and documentation of...

Job Summary:Calibre Scientific is seeking a highly skilled Regulatory Engineer to join our team in the role of Environmental Validation Solutions Specialist. As a key member of our team, you will be responsible for conducting testing and inspection at client sites, troubleshooting, and repairing systems as necessary, and preparing accurate reports and...

As a Senior Manufacturing Engineer for Standards Validation Documentation at CHEP, you will lead efforts to establish and maintain manufacturing standards, validation processes, and documentation practices across our global engineering and future automation teams. Leveraging your expertise in engineering standards, validation methodologies, and documentation...

As a Senior Manufacturing Engineer for Standards Validation Documentation at CHEP, you will lead efforts to establish and maintain manufacturing standards, validation processes, and documentation practices across our global engineering and future automation teams. Leveraging your expertise in engineering standards, validation methodologies, and documentation...

As a Senior Manufacturing Engineer for Standards Validation Documentation at CHEP, you will lead efforts to establish and maintain manufacturing standards, validation processes, and documentation practices across our global engineering and future automation teams. Leveraging your expertise in engineering standards, validation methodologies, and...