compliance and training systems. Ensure compliance with global regulatory requirements such as FDA, EMA, ISO 13485, GMP...’s pharmaceutical and medical device operations. This role ensures adherence to global regulatory requirements, industry standards...
Lugar:
El Paso, TX | 30/01/2026 01:01:21 AM | Salario: S/. No Especificado | Empresa:
BD a global team of MSAT E2E Product Leads who represent MSAT in Strategic Operations Teams (SOTs) and provide cross-functional... alignment and performance monitoring between global MSAT leadership, site MSAT teams, and cross-functional partners in Quality...
Lugar:
Boston, MA | 27/01/2026 19:01:20 PM | Salario: S/. No Especificado | Empresa:
Servier Scientific, partnering cross-functionally with Operations, Engineering, Regulatory, and Supply Chain teams to ensure quality..., you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission...
Do You will be part of a dynamic, cross-functional global team delivering strategic consulting engagements for leading Life Sciences.... Here are some engagements our Life Sciences consultants are working on: Leading digital transformation programs for global pharmaceutical firms...
and quality management Strong understanding of cGMP regulations, quality systems, and global regulatory expectations (FDA, EMA... efficient resource allocation Quality & Regulatory Compliance: Ensure adherence to cGMP, ICH GCP, FDA, EMA guidelines;manage...
& Inspection Readiness Ensure full compliance with GMP, GDP, ICH, FDA, EMA, and global regulatory requirements Maintain... SUMMARY The Vice President, Supply Chain is responsible for the end-to-end strategy, execution, and governance of global...
harmonization and standardization across global sites to ensure compliance with regulatory requirements (e.g., FDA, EMA, ICH, ISO... of global quality systems that support compliance, operational excellence, and risk mitigation across the pharmaceutical product...
Lugar:
USA | 22/01/2026 18:01:53 PM | Salario: S/. No Especificado | Empresa:
Otsuka, and validation master plans/reports. As member of globalengineering team, strongly connecting and involving in DP global... regulatory and quality standards (FDA, EMA, ICH) and are in a state of control throughout their lifecycle. The ideal candidate...
, protocols (DQ, IQ, OQ, PQ) summary reports, and validation master plans/reports. As member of globalengineering team, strongly... connecting and involving in DP globalengineering projects planning and implementation. Regulatory Compliance Ensure all CQV...
assessment, protocols (DQ, IQ, OQ, PQ) summary reports, and validation master plans/reports. As member of globalengineering... team, strongly connecting and involving in DP globalengineering projects planning and implementation. Regulatory...