26/04/2024 | Fulltime | Dublin | CV-Library | €100,000 - €120,000 / Year Progress and financial performance, ensuring compliance with contractual obligations and regulatory requirements. - Resolve disputes and claims in a timely and cost-effective manner, maintaining positive relationships with all parties involved. - Provide guidance and support to project teams on contract
Save for later22/04/2024 | Fulltime | Dublin | CV-LibraryThe implementation of data retention policies and procedures to ensure compliance with regulatory requirements and best practices. - Drive innovation within the organization by exploring and implementing new technologies and methodologies. - Proficiency in programming languages such as JavaScript, C#, Python
Save for later26/03/2024 | Fulltime | Dublin | CV-Library | €77,100 - €111,400 / Year Regulatory Affairs Manager. Join them in driving technological advancements in wound care and shaping the future of their organisation. As the new Regulatory Affairs Manager, you will be responsible for developing Regulatory Strategies, MDR compliance, Product Changes and New Product Submissions
Save for later05/03/2024 | Fulltime | Dublin | CV-LibraryAnd finished drug products, deviation, complaint, and change control record management. Responsibilities • Manage contractor quality assurance activities to ensure product is manufactured, packaged, tested, released, and distributed in compliance with all regulatory and corporate requirements. • Leading
Save for later16/02/2024 | Fulltime | Dublin | CV-LibraryOn large construction projects. - Thorough understanding of large process operations with a working knowledge of environmental and waste management regulations and the implementation best practice standards for waste management including solid and liquid waste disposal, and other environmental aspects
Save for later16/02/2024 | 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
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