08/01/2021 | Fulltime | Dublin | CV-LibraryAnd suggestions to improve standard laboratory techniques, improve protocols, processes and equipment Execute microbiological validations as needed for products and processes Ensure products and processes with Micro laboratory comply with procedures and the principles of GMP Support and assist in internal
Save for later11/01/2021 | Fulltime | Dublin | CV-LibraryManagement of capital projects in the Pharma industry. Ability to manage either a significantly large project or portfolio of projects and demonstrated ability to achieve results Proven knowledge, appreciation and experience of working in a strongly regulated GMP environment. Experience in lean six sigma
Save for later07/01/2021 | Fulltime | Dublin | CV-Library | €45,300 - €72,500 / Year Departments and locations regarding GMP Document review and finished product releases. In particular, this will involve partnering with major stakeholders such as Operations, QC, Facilities, Engineering and Supply Chain to optimize patient supply. What you will be doing - Provide quality and cGMP input
Save for later06/01/2021 | Fulltime | Dublin | CV-LibraryRole must ensure effective interaction with other departments and locations regarding GMP Document review and finished product releases. In particular, this will involve partnering with major stakeholders such as Operations, QC, Facilities, Engineering and Supply Chain to optimise patient supply. Role
Save for later07/01/2021 | Fulltime | Dublin | CV-Library | €63,400 - €90,600 / Year Or equivalent in Biological - Chemical sciences, or a related pharmaceutical science field or equivalent experience in a regulated industry - Minimum of 10 years’ experience in a cGMP environment preferably within a Quality Management role within biopharma - Direct experience of GMP documentation management
Save for later07/01/2021 | Fulltime | Dublin | Adaptive HVM Ltd | This key role must ensure effective interaction with other departments and locations regarding GMP Document review and finished product releases. In particular, this will involve partnering with major stakeholders such as Operations, QC, Facilities, Engineering and Supply Chain to optimize patient supply
Save for later22/12/2020 | Fulltime | Dublin | CV-LibraryProtein Concentration, Polysorbate, Moisture and Device testing) GC (Gas Chromatography) testing is a good one, moisture testing, use of a UV. At least 4 of the ones called out need experience with. GMP pharma is a MUST, right first time, good documentation practices. Ideal candidate with had continuous
Save for later04/12/2020 | Fulltime | Dublin | CV-LibraryOf microbiological techniques, including but not limited to Bioburden, Endotoxin, Sterility (in an Isolator), Environmental Monitoring, Rapid Micro techniques, Microbial Identification, Media prep, Water Sampling. Understanding and application of principles, concepts, theories and standards of GMP QC microbiology
Save for later08/12/2020 | Fulltime | Dublin | CV-Library | €59,300 - €63,900 / Year Relevant qualifications in Facilities Management, Engineering or Technical Services would be an advantage. - Familiarity with pharmaceutical, FMCG or GMP processes. - Experience leading Facilities Management projects from start to finish. - Able to liaise with colleagues and clients to manage relationships
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