1,820 ofertas de regulatory en toda España.

... audits across pharmaceutical and biotech operations. The role involves conducting GxP audits, managing CAPA plans, providing quality consulting, and supporting regulatory compliance for the company and its clients. Responsibilities - Conduct internal and contracted audits of company partners, vendors, investigative sites, and ...

... audits across pharmaceutical and biotech operations. The role involves conducting GxP audits, managing CAPA plans, providing quality consulting, and supporting regulatory compliance for the company and its clients. Responsibilities - Conduct internal and contracted audits of company partners, vendors, investigative sites, and ...

... audits across pharmaceutical and biotech operations. The role involves conducting GxP audits, managing CAPA plans, providing quality consulting, and supporting regulatory compliance for the company and its clients. Responsibilities - Conduct internal and contracted audits of company partners, vendors, investigative sites, and ...

Thermo Fisher Scientific seeks an experienced GCP Quality Assurance Auditor III to conduct clinical audits, ensure regulatory compliance, and support quality standards across EMEA regions. The role involves leading audits, providing GCP consultation, and presenting findings to internal and external stakeholders, with travel ...

Thermo Fisher Scientific seeks an experienced GCP Quality Assurance Auditor III to conduct clinical audits, ensure regulatory compliance, and support quality standards across EMEA regions. The role involves leading audits, providing GCP consultation, and presenting findings to internal and external stakeholders, with travel ...

... activities across Spain and Portugal. Role involves pre-study through close-out visit management, investigator qualification verification, site staff training, and regulatory submission support for Phase 2/3 clinical trials. Responsibilities - Conduct pre-study, initiation, interim, and close-out monitoring visits at investigational ...

... across clinical trials in Madrid. The role encompasses site monitoring, protocol compliance oversight, and quality assurance to support patient safety and regulatory standards throughout trial conduct and close-out. Responsibilities - Monitor assigned investigator sites from initiation through database lock, ensuring protocol ...

... and supplier/customer/technology agreements. Flag risks early and land practical, business-friendly solutions. - Drive product forward: Translate legal and regulatory requirements into clear guidance for new product lines. Research regulatory requirements and use them to develop product specs. Review designs end-to-end to ...

... IQVIA and client’s in their use. - Assures that work delivered to clients meet minimum submission requirements as defined by FDA Guidance Documents and other regulatory guidance. - Guide clients in their use of CDISC standards through governance teams. - Monitors regulatory authority and standards organization sites for updates ...

... environment. Responsibilities - Design, develop, and maintain Murex DataMart extractions (reports, feeds, and data exports) for Back Office, Risk, Finance, and Regulatory reporting needsBuild and support integration interfaces between Murex Mx.3 and external systems (e.g., general ledger, settlement platforms, risk engines, ...

... environment. Responsibilities - Design, develop, and maintain Murex DataMart extractions (reports, feeds, and data exports) for Back Office, Risk, Finance, and Regulatory reporting needsBuild and support integration interfaces between Murex Mx.3 and external systems (e.g., general ledger, settlement platforms, risk engines, ...

... execution and clearing. The business has grown strongly over the last few years and consequently we are currently establishing an office in New York (subject to regulatory approval). Further evidencing our ambition, BBVA recently announced the purchase (subject to regulatory approval) of the 50% of Altura Markets in Spain that ...

... improvement initiatives to solve complex manufacturing or quality challenges while driving alignment between supplier operations and Roche strategic goals. - Regulatory Landscape & Intelligence: Communicate updated regulatory requirements and Roche expectations to GxP suppliers, evaluating site quality systems for ongoing ...

... launch to embed privacy-by-design principles, responsible AI practices, and proportionate risk controls into product features and operational workflows. - Regulatory interpretation and practical guidance: Translate complex legal and regulatory requirements into clear product guidance, internal policies, review frameworks, ...

... spoken) - More than 5 years of work experience in Pharma Industry (in depth knowledge preferably in technology transfers, product development, manufacturing, or regulatory affairs). It can independently manage all areas of Tech Transfer Projects: quality, regulatory and technical - Project management experience and capability ...

... across a fast-paced, global environment. Job Description Key Responsibilities - Manage submission-readiness of clinical documents, ensuring compliance with regulatory requirements and quality standards - Oversee technical editorial and formatting of clinical documents for regulatory submissions - Ensure clinical documentation ...

... including risk appetite and balance sheet management - Ensuring the firm is compliant with all aspects of MiFIDPRU and defining responses to financial risk regulatory changes - Developing and implementing the ICARA process - Ensuring our risk management framework is properly embedded, including risk identification, control ...

... leadership, stakeholder management, and collaboration skills* Ability to manage risk and drive strategic decision-making* Experience developing clinical or regulatory documentation* Strong scientific and analytical capabilities within life sciences**Desirable Requirements*** Experience supporting global regulatory submissions ...

... motivated individual with real-world life science industry experience in Regulatory Operations or Regulatory Affairs to drive customer success with our Veeva Regulatory Information Management (RIM) products in Europe. If you are a person who has a blend of experience building regulatory submissions and understanding of the ...

... the Senior Product Manager for Sovereign Services, you will lead the development of Vodafone's sovereign services operating model, ensuring it meets both EU regulatory requirements and the sovereignty requirements of our customers. You will define how our sovereign services are designed, governed, delivered and assured end-to-end ...