QA Validation Specialist - Limerick
1 week ago

Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
Working with the QA Validation team you will be responsible for validating systems and processes in accordance with regulatory requirements. Your role will involve supporting, following and implementing company manufacturing standards policies and procedures. · Have demonstrated ...
1 week ago
+Validate systems and processes in accordance with regulatory requirements. · ...
1 week ago
The QC Validation Specialist is responsible for the validation and technology transfer of novel and established test methods for the analysis of gene therapy products. · To support the development and validation of established and novel analytical test methods. · Generate validat ...
4 weeks ago
We're supporting a growing gene therapy manufacturing site in Shannon with the hire of a QC Validation Specialist to strengthen analytical method validation and transfer into GMP QC laboratories. · ...
4 weeks ago
Ensuring analytical excellence at the forefront of gene therapy innovation. · ...
4 weeks ago
We're supporting a growing gene therapy manufacturing site in Shannon with the hire of a QC Validation Specialist to strengthen analytical method validation and transfer into GMP QC laboratories. · This is a hands-on onsite role suited to someone who has direct experience writing ...
4 weeks ago
Ensuring analytical excellence at the forefront of gene therapy innovation. · Lead the design, authorship, execution, and review of analytical method validation studies. · ...
4 weeks ago
The QC Validation Specialist is responsible for the validation and technology transfer of novel and established test methods for the analysis of gene therapy products. · Degree or Master's in human health or Sciences. · Experience in an analytical methods/validation role. · ...
1 month ago
The QC Validation Specialist is responsible for the validation and technology transfer of novel and established test methods for the analysis of gene therapy products and associated materials used for manufacturing EU and FDA GMP requirements. · Generate validation test protocols ...
1 month ago
The QC Validation Specialist is responsible for the validation and technology transfer of novel and established test methods for the analysis of gene therapy products and associated materials used for manufacturing EU and FDA GMP requirements. · ...
4 weeks ago
The QC Validation Specialist is responsible for the validation and technology transfer of novel and established test methods for the analysis of gene therapy products and associated materials used for manufacturing EU and FDA GMP requirements. · To support the development and val ...
1 week ago
We are seeking a Test Method Validation Specialist to lead the creation and development of comprehensive test method validation/transfer programs. · Lead the creation and development of test method validation/transfer programServe as QC single contact between test method transfer ...
2 weeks ago
You will lead the following functions within the Quality Team concerning customer and quality requirements to develop Organic Light Emitting Diodes: test method validation/transfer, test method qualification/verification, definition of method LOD/LOQ and system suitability requir ...
1 month ago
++Computer system validation specialist required for multinational life sciences client in Limerick. · ++Validation Planning and Execution, · Regulatory Compliance. · Testing and Verification. · , ...
1 month ago
This is a contract role on an initial 12 month contract. Hybrid working available with minimum 3 days on site in Limerick required. · ...
1 month ago
Looking for experienced Senior Validation Engineers to support commissioning, qualification, and validation activities at a pharmaceutical site. · ...
1 month ago
We are looking for kind enthusiastic dedicated individuals who are passionate about working with children to join our team. · Accompany the child · Help them develop their social skills · Encourage them to use a positive communication style · ...
1 month ago
We're looking for a Principal Operations Specialist (IT Business Process Automation) to lead ServiceNow and ProcessX automation for IAM and QAR in a GxP environment. · Design, build, and maintain automated workflows in ServiceNow and ProcessX to improve operational efficiency an ...
2 weeks ago
About Direct Medics · This year, we're proud to celebrate our 25th anniversary, marking a quarter-century of placing healthcare professionals in locum roles across both the public and private sectors in the UK and Ireland. Our long-standing reputation speaks to the trust and reli ...
1 week ago
This position will primarily be based in Limerick and the role of Project Manager - Civil Construction is to develop and maintain detailed project schedules using industry-standard planning software. · ...
1 month ago