01/03/2024 | 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
Save for later13/11/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGRequirements - Must have a third level qualification in Engineering/Quality/Science. - Must have 2+ years work experience in a Medical Device manufacturing environment. - A working knowledge of quality systems such as ISO 13485 is essential. Experience and knowledge of 21 CFR Part 820 and EU GMP
Save for later16/06/2021 | Fulltime | Dublin | JobsIrelandPractice, rules & regulations are in place & operating on site. • Conduct traceability exercises as required. • Provide regular Supplier quality performance reports to assist production managers eliminate non-conformance. • Hygiene checks and GMP throughout floors. • Generating MSR’s for Held stock
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