22/06/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | And experimental design Good Communication skills, both written and oral Strong technical writing skills Ability to train/facilitate Knowledge and implementation of medical device Quality System requirements (FDA and ISO) and Good Manufacturing Practice preferred Knowledge of Lean and Six Sigma principles
Save for later19/06/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Standards that meet Medical Device manufacturing role provides an excellent opportunity for career development and to gain further experience within a highly automated and high volume regulated/medical device production process. Responsibilities New Machinery Development (80
Save for later16/06/2024 | Fulltime | Ballina (Munster) | TipTopJob Ireland | Necessary 58 Relevant experience in the medical device industry or equivalent regulated industry People Management experience desirable Education Requirements Degree in Engineering/Science Discipline and Quality Engineering Qualification or equivalent Certified Quality Engineer qualification
Save for later15/06/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Business efficiency. Contribute to fostering a culture of innovation through identifying innovative solutions to process problems and actively encouraging team members to share new ideas. Work Experience Requirements stylemarginbottom4.0px;margintop4.0px 4+ years' experience preferably in medical
Save for later15/06/2024 | 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 later12/06/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | In a relevant science discipline (e.g. biochemistry, 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
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