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Life Science Consultants in Ireland is seeking a Quality Risk Management Lead for a 12-month contract at a state-of-the-art Limerick biopharma campus. If you want to know about the requirements for this role, read on for all the relevant information. You will design and implement a GMP-compliant QRM framework aligned with ICH Q9(R1), lead cross-functional...

Job Description Are you ready to be at the forefront of biotechnology excellence? LSC have a fantastic contract opportunity for a Quality Risk Management Lead to join an innovative and rapidly growing biopharmaceutical company at their state-of-the-art campus in Limerick. This company is transforming lives through groundbreaking medicines that treat serious...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with...

Basic Role Summary: For a complete understanding of this opportunity, and what will be required to be a successful applicant, read on. This role offers a unique opportunity to be an analytical method development scientist within a dynamic pharmaceutical R&D Medical team. You will be instrumental in supporting Chanelle Pharma's vision to be the most valued...

RegionalteamleiterIn Servicetechnik (100%) Dein Aufgaben- und Verantwortungsbereich: Do not wait to apply after reading this description a high application volume is expected for this opportunity. Du bist eine Führungspersönlichkeit mit Leidenschaft für exzellenten Service und einem Blick fürs Detail? Dann erwartet dich eine spannende Herausforderung...

QA QUALITY RISK MANAGEMENT LEAD, DIGITAL CORE IMPLEMENTATION required by CareerWise Recruitment for our Life Sciences client in Limerick.Initial 12 month contract on offer with site presence required 5 days per week on-site.This role sits within the Quality Assurance group.Strong knowledge of ICH Q9, digital manufacturing concepts required.Experience...

- Design and implement a modern, facility-wide Quality Risk Management (QRM) framework, aligned with ICH Q9(R1), supporting a fully digital plant. - Embed risk-based thinking into all aspects of facility startup, including manufacturing processes, digital systems, automation, data flows, and quality oversight. - Assess and manage risks related to dependency...

Workplace: on‑site (Limerick) While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required. Workload: Full‑time Type of Contract: B2B Key Responsibilities - - Design and implement a modern, facility‑wide Quality Risk Management (QRM) framework, aligned...

Charles River Laboratories is seeking an experienced Project Leader for its Biologics Division in Ballina, Ireland. The role involves leading analytical development activities, validating methods per ICH guidelines, and coordinating with Quality and clients to ensure GMP compliance and successful study execution.The candidate will design studies, manage...

Regeneron Pharmaceuticals seeks a Clinical Supply Operations Specialist to support the Clinical Drug Supply & Logistics team in a hybrid Dublin role. You will manage investigational product supply, inventory planning and documentation across multiple therapeutic areas, coordinating with QA, regulatory and external stakeholders to ensure uninterrupted study...

Thermo Fisher Scientific in Ireland seeks a Supervisor, Biopharma to lead the Biopharmaceutical team in our Analytical GMP labs, overseeing daily activities, staffing, and resource planning to meet quality and turnaround objectives. xlwxzce Please make an application promptly if you are a good match for this role due to high levels of interest. You will...

Hovione in Ireland seeks a Quality Control Supervisor to lead a highly technical QC team, ensuring high-quality analytical services and compliance with GMP/ICH. The role emphasizes developing people, pursuing operational excellence, and maintaining safety and quality standards across materials, intermediates, and finished products. You will drive continuous...

CareerWise Recruitment is seeking a QA Quality Risk Management Lead for a Life Sciences client in Limerick. This is a 12-month contract with on-site presence five days per week, within the Quality Assurance group, to implement a digital QRM framework across the facility.The successful candidate will bring extensive GMP QRM experience, strong ICH Q9...

IQVIA in Ireland seeks an Associate Director of Quality, Client Dedicated – Regional Clinical Compliance Inspection, to lead proactive risk management and sustained inspection readiness across clinical trials. Hit Apply below to send your application for consideration Ensure that your CV is up to date, and that you have read the job specs first. The role...

Cardinal Health Ireland seeks a Medical Writer to develop regulatory and scientific documents for regulatory filings including CTD Module 2 summaries and CSRs. Do you have the right skills and experience for this role Read on to find out, and make your application. You will work with submission teams and document specialists to ensure accuracy and timely...

Regeneron Pharmaceuticals, Inc. in Dublin seeks a Senior Manager for Global Patient Safety to shape safety strategies for molecules in development and post-marketing. You will lead signal detection and evaluation, and prepare DSUR/PSUR/RMP while collaborating with cross-functional teams. The role requires 7+ years in risk management in pharma/biotech,...

Fastnet is seeking an Analytical / QC Technology Transfer Specialist for a 12-month contract in Tralee, Co. Kerry. You will own the analytical workstream for product transfers, focusing on method transfer and verification within a GMP environment.The role requires 4+ years of QC/Analytical experience, familiarity with analytical method transfer/verification...

EFOR seeks a seasoned CQV Lead to manage end-to-end Commissioning, Qualification, and Validation activities for pharmaceutical manufacturing projects with DeltaV automation. Experience in spray dryer operations is highly preferred.You will develop CQV documentation, lead cross-functional teams, and ensure GMP readiness for regulatory audits. The role...

McKesson is seeking a Drug Safety & Pharmacovigilance Specialist based in Cork, Ireland to lead day-to-day safety activities for our private label portfolio. You will log, assess, investigate, and report adverse events, maintain safety data exchange with suppliers, and ensure FDA/ICH compliance within a growing Regulatory Affairs team.The role requires...

DPS Group Global is seeking a Process Engineer to support capital projects on site, providing technical oversight of CQV activities and ensuring GMP principles are applied throughout project delivery.The successful candidate will have a Bachelor's degree in Engineering and at least 5 years' CQV experience in a regulated pharma setting, with strong CQAs/CPPs,...