16/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | In compliance with regulatory and corporate requirements. A significant feature of this role is to minimize equipment downtime thus optimizing overall plant performance. Responsibilities stylemarginbottom4.0px;margintop4.0px Provide high level technical support in a highvolume environment and work
Save for later08/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Support to other functions including Global Marketing, Regulatory Affairs, Engineering and Manufacturing. Managing project schedules, conducting product and project risk analysis and ensuring successful and timely completion of project activities. Working with patent counsel to support patentability
Save for later08/05/2024 | Fulltime | Ballina (Munster) | TipTopJob Ireland | Biotechnology or biology) 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. Analytical techniques experience essential. Experience in development and validation of analytical
Save for later08/05/2024 | Fulltime | Ballina (Munster) | TipTopJob Ireland | Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry. Experience in project management essential. BSc/M.Sc. in a
Save for later08/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Engineering Skills/Technical Knowledge Experience with computerized calibration and PM systems (Blue Mountain preferred) Experience working as a team to achieve department and site goals Experience liaising with other departments to schedule/coordinate work Experience with regulatory compliance
Save for later01/05/2024 | Fulltime | Ballina (Connacht) | 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) | TipTopJob Ireland | And viability) Provide technical training to team as required. Receipt and processing of test samples in LIMS. Update current standard operating procedures. Assist in laboratory investigations where necessary. Responsible for reporting progress information to Management. Assist in internal, regulatory
Save for later01/05/2024 | Fulltime | Ballina (Connacht) | 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) | 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
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