16/02/2024 | Fulltime | Dublin | CV-LibraryKnowledge of regulatory guidelines, such as FDA 21 CFR Part 11, EU Annex 11, and GAMP 5. - Experience in computer system validation within a regulated industry, preferably pharmaceuticals or biotechnology. - Familiarity with validation methodologies, including risk-based validation approaches. - Proficiency
Save for later19/05/2024 | Fulltime | Dublin | Reemtsma Cigarettenfabriken GmbHAnd Regulatory) to deliver fit for purpose propositions (Consumer, Cost, Scalability) and ensure technical requirements are clearly understood. - Develop strong relationships with partners and suppliers to enable access to newest and most appropriate technologies and facilitate prototype production and scale up
Save for later19/05/2024 | Fulltime | Dublin | Reemtsma Cigarettenfabriken GmbHAnd Regulatory) to deliver fit for purpose propositions (Consumer, Cost, Scalability) and ensure technical requirements are clearly understood. - Develop strong relationships with partners and suppliers to enable access to newest and most appropriate technologies and facilitate prototype production and scale up
Save for later05/05/2024 | Fulltime | Dublin | Reemtsma Cigarettenfabriken GmbHAnd manufacturing of innovative products, including brand quality upgrades, product maintenance, regulatory labelling changes, strategic supply chain, and cost-saving initiatives. Being based in either our Amsterdam, Warsaw, Radom, Tarnowo or Bristol office - This integral Product Realisation Project Manager role
Save for later07/04/2024 | Fulltime | Dublin | Reemtsma Cigarettenfabriken GmbHOf the team. - Work closely with multifunctional counterparts (Marketing/Category, MSC, Quality and Regulatory) to deliver fit for purpose propositions (Consumer, Cost
Save for later07/04/2024 | Fulltime | Dublin | Reemtsma Cigarettenfabriken GmbHOf the team. - Work closely with multifunctional counterparts (Marketing/Category, MSC, Quality and Regulatory) to deliver fit for purpose propositions (Consumer, Cost
Save for later13/11/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGManager within Operations this role ensures internal system compliance and customer specifications conformity. Complaint Reporting Specialist to support complaint handling and regulatory reporting activities. This role will ensure the timely and effective closure of internal/external complaint handling
Save for later12/06/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGLed giving program. Job Summary Responsibility for compliance with the Quality and Regulatory requirements for combination medicinal and device products assembled and packed by West CM (Dublin). This role is also responsible for overseeing the compiling of technical and quality documents in support
Save for later19/06/2021 | Fulltime | Dublin | Irish FutureOf students or other staff, as assigned to you by management - To comply with all regulatory and legal requirements relevant to rehabilitation - To comply with the implementation of objectives and standards which guide the staff of the Company in the delivery of innovative and high quality treatment, care
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