1 job found in tullamore, offaly

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    • tullamore, offaly
    • temporary
    • €30,000 - €35,000 per year
    • full-time
    We are currently recruiting for a number of exciting roles in Offaly. Our client is one of the leaders in global pharmaceuticals and is growing substantially. We are looking for QC Analysts, QA Specialists, Analytical Scientists, Production Operatives, Process Scientists and Technical Reviewers to join this fantastic team. Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D. POSITION SUMMARYProvide scientist level expertise to support analytical technology covering a range of active pharmaceutical ingredients. POSITION RESPONSIBILITIES Key objectives of this position include:Perform testing of in-process, final product, and stability of drug substance and drug product samples using a suite of protein-specific analytical methods (CGE, SEC-HPLC, cIEF, ELISA) and general analytical methods (appearance analysis, pH, conductivity, etc.).Microbiological analysis including Environmental Monitoring, Endotoxin and Bioburden testing, growth promotion, and other associated tests.Support the technical transfer of analytical test methods to and from the Tullamore facility.Creation and revision of documents including test methods, SOPs, material requirement specifications, forms, and other quality system documentation to allow the execution of the analysis in a GMP environment. This will include trending data, monitoring Out of Specifications and participating in laboratory investigations.Work closely with the process development group to support the development of a robust manufacturing process.Work closely with specialist contract testing service providers to ensure excellent collaboration is maintained throughout the project.Support raw material testing (and outsourcing activities) to E.P./USP monographs when required for GMP manufacture.Input into the identification of equipment requirements and work with vendors to ensure execution of all deliverable, including equipment qualification and validation.Provide technical reports upon completion of QC projects.Participate in Quality and Safety regulatory audits. EDUCATION AND EXPERIENCE BS degree in chemistry, or analytical / chemical engineering is required; a post-graduate qualification within analytical sciences may be advantageous.Industry experience, minimum of 1 years of process chemistry experience.Mastery of scientific principles, practices and theories with broad analytical experience, such as method development / troubleshootingFamiliarity with commercial scale processes and analytical techniques is desiredSkilled in applying statistical methods to analytical method performance characteristics Demonstrated ability to work effectively in a cross functional and culturally diverse work environment. This is a 12 month contract role with a view to permanency and progression. If you would like to learn more about this opportunity please contact Dannielle or Lisa, our Life Science Specialists. dannielle.beggs@randstad.ie lisa.mccarrollquinn@randstad.ie Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
    We are currently recruiting for a number of exciting roles in Offaly. Our client is one of the leaders in global pharmaceuticals and is growing substantially. We are looking for QC Analysts, QA Specialists, Analytical Scientists, Production Operatives, Process Scientists and Technical Reviewers to join this fantastic team. Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D. POSITION SUMMARYProvide scientist level expertise to support analytical technology covering a range of active pharmaceutical ingredients. POSITION RESPONSIBILITIES Key objectives of this position include:Perform testing of in-process, final product, and stability of drug substance and drug product samples using a suite of protein-specific analytical methods (CGE, SEC-HPLC, cIEF, ELISA) and general analytical methods (appearance analysis, pH, conductivity, etc.).Microbiological analysis including Environmental Monitoring, Endotoxin and Bioburden testing, growth promotion, and other associated tests.Support the technical transfer of analytical test methods to and from the Tullamore facility.Creation and revision of documents including test methods, SOPs, material requirement specifications, forms, and other quality system documentation to allow the execution of the analysis in a GMP environment. This will include trending data, monitoring Out of Specifications and participating in laboratory investigations.Work closely with the process development group to support the development of a robust manufacturing process.Work closely with specialist contract testing service providers to ensure excellent collaboration is maintained throughout the project.Support raw material testing (and outsourcing activities) to E.P./USP monographs when required for GMP manufacture.Input into the identification of equipment requirements and work with vendors to ensure execution of all deliverable, including equipment qualification and validation.Provide technical reports upon completion of QC projects.Participate in Quality and Safety regulatory audits. EDUCATION AND EXPERIENCE BS degree in chemistry, or analytical / chemical engineering is required; a post-graduate qualification within analytical sciences may be advantageous.Industry experience, minimum of 1 years of process chemistry experience.Mastery of scientific principles, practices and theories with broad analytical experience, such as method development / troubleshootingFamiliarity with commercial scale processes and analytical techniques is desiredSkilled in applying statistical methods to analytical method performance characteristics Demonstrated ability to work effectively in a cross functional and culturally diverse work environment. This is a 12 month contract role with a view to permanency and progression. If you would like to learn more about this opportunity please contact Dannielle or Lisa, our Life Science Specialists. dannielle.beggs@randstad.ie lisa.mccarrollquinn@randstad.ie Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003

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