01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | With ICH guidelines, where appropriate. Draw up study plans and implement studies in strict accordance with study plan ensuring full GMP regulatory compliance as appropriate. Liaise with the Quality Department for the generation of audit responses, deviation reports and for the compilation of study
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | In a relevant science discipline (e.g. Cell Culture or Immunoassays) A minimum of 2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry. Experience in invitro bioassays and project management highly
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | Generation of GMP compliant Data capture forms, SOPs, Protocols and reports.- Carry out data calculations and simple statistics. Assist in internal, regulatory and client visits/audits and respond to findings Sourcing, purchasing and stocking consumables, standards and reagents required for testing
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | Microplate assays or client specific immunoassays. Safe and compliant disposal of all laboratory generated waste. Profile and Requirements The following are minimum requirements related to thisPosition; A minimum of 2 years relevant experience in Scientific Research preferably within a GMP regulated
Save for later01/05/2024 | Fulltime | Ballina (Connacht), Ballina (M | TipTopJob Ireland | regulatory requirements are fulfilled. - Manage direct reports to assure that Quality Assurance responsibilities of applicable regulations are fulfilled. - Assure staff receives
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