27/04/2024 | Fulltime | Longford | CV-LibraryFor vendor and client Perform IQ,OQ,PQ, FAT's, SAT's, GMP reviews, Risk Assessments, Change Controls, and regulatory auditsAbout you Qualification in Engineering, Science, or equivalent Manufacturing experience across Medical Devices or Plastics A minimum of 2 years' experience as a Validation Engineer
Save for later23/04/2024 | Fulltime | Dublin | CV-Library | €47 - €52 / Hour Generation, Clean Steam, Waste Inactivation. - Knowledge of Process systems; Centrifuge, Parts Washers, Autoclaves. - An understanding of applicable regulations such as Annex 11, GAMP and 21 CFR Part 11. - 7+ years’ experience in a GMP environment, preferably Pharma/Biopharma. - Strong problem solving skills
Save for later04/04/2024 | Fulltime | Athlone (Leinster) | TipTopJob Ireland | And professional manner. To scope out and or assist in the scoping out of Projects. To get quotations and pricing agreements from the necessary contractors Ensure the firstclass performance and further development of the site, managing specialist subcontractors to meet our contract KPIs/SLAs. GMP/GxP Quality
Save for later05/04/2024 | Fulltime | Kildare | CV-Library | €22 - €28 / Hour To work safely in industrial environments Knowledge of Good Manufacturing Practices (GMP) working environment Strong mechanical aptitude, troubleshooting skills, and or hands-on electrical/electronic experience Proficient in using MS Office (Excel, PowerPoint, Word) Excellent communication skills
Save for later09/04/2024 | Fulltime | Louth | CV-LibraryOf the organization. If you are a confident, experienced, and adaptable Health & Safety professional looking for a challenging yet rewarding opportunity, we encourage you to apply today! Key Words H&S, health and safety, EHS, manufacturing, production, plant, GMP, NEBOSH, IOSH, risk assessment, hazards, root cause
Save for later01/03/2024 | Fulltime | Dublin | CV-Library· Prepare contract documentation, specifications, and drawings. · Ensure alignment with project requirements and industry standards. Requirements · Bachelor's Degree in Engineering or Relevant Experience · Typically, 3+ years engineering experience, preferably within a GMP manufacturing environment
Save for later05/03/2024 | Fulltime | Dublin | CV-Library• Review batch records, both master production/packaging records and executed batch records ensuring compliance with GMP and registration requirements. • Manage change control requests. This includes, as necessary • Process product complaints. • Review, edit, negotiate improvements to, and approve
Save for later16/01/2024 | Fulltime | Dublin | CV-LibraryIn CSV and/or CQV for laboratory systems and instrumentation - Experience in regulatory audits. - Working knowledge of biologics analytical methods and specifications and Good Manufacturing Practice (GMP). - Strong CSV experience with analytical instrument maintenance - Excellent understanding of data
Save for later20/11/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGOf responsibility. The Quality Specialist, Compliance will provide training and analytical support in the operation of the relevant GMP systems (MasterControl, SAP etc.). The Quality Specialist, Compliance is responsible for supporting the onboarding of new hires including participation in the Induction Programme
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