Calling all innovators – find your future at Fiserv. We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations,
Job Description SummaryAs a Shift QA Specialist at GE HealthCare, you will play a key role in ensuring the highest quality and compliance standards across our manufacturing operations. Working closely with Operations, QC, and cross-functional teams,
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes
Calling all innovators – find your future at Fiserv. We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations,
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes
Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle
Job Description Are you passionate about biotechnology and eager to make a meaningful impact on patients lives? We are looking for a Senior Specialist in Manufacturing Science and Technology to join our Process Engineering team at
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter –
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Compliance Specialist - Make an Impact at the Forefront of Innovation! Position overview: The Compliance Specialist executes quality and compliance processes across the organization and
McDermott Laboratories Limited Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to
About the Role We are seeking an experienced Systems Engineer to support the technical upgrade of clients hosted Charles River Investment Management Solution (CRIMS) environments. This is a hands on technical role working across enterprise applications,
Job title: Quality Analyst Microbiology Location: Waterford, Ireland Contract type: Fixed term 12 months About the Job As Quality Analyst Microbiology within our QC Team, you’ll provide chemistry support and knowledge to the QC team and
Location: Waterford, Ireland Working pattern: Full-time, onsite, with some opportunity to work from home depending on the role and business needs Contract: 23-month Fixed-Term Contract Programme start: October 2026 About the opportunity Are you a recent
Job Title: Process Engineer (Pre-Filled Syringe Manufacturing) Location: Waterford, Ireland Job Type: 23-month Fixed Term Contract Work Arrangement: On-site Shift: Standard Days Role About the job As a Process Engineer, you will provide engineering support for
Job Title: Process Engineer in Fill Finish Fill Operations, 24/7 Location:Waterford, Ireland Job Type:23-month Fixed Term Contract Work Arrangement:On-site Shift:24/7 – 2 Days, 2 Nights, 4 Days Off (12-hour Shifts) About the role As a Process
Your mission As the QC Compliance Specialist, you will be responsible for ensuring continued Good Manufacturing Practice (GMP)-compliant activities within QC to support the manufacture of gene therapy products. Review and Approve QC documentation to support
Your missionAs QC Specialist, you will be responsible for ensuring continued Good Manufacturing Practice (GMP) – compliant activities within QC to support the manufacture and release of plasmids and gene therapy products. This role will be a
Your missionAs the QC Senior Compliance Specialist, you will be responsible for ensuring continued Good Manufacturing Practice (GMP)-compliant activities within QC to support the manufacture of gene therapy products. Review and Approve QC documentation to support
Are you an experienced Team Leader or Project Manager with an engineering, construction, MEP or electrical background looking for your next challenge? We’re looking for a commercially aware and delivery-focused Project Manager Team Lead to provide