p pOxford Global Resources is seeking a bGlobal CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company /b to support headquarters in Barcelona through our consulting services division. /p h3Key Responsibilities /h3 ul liProvide CMC regulatory insight and advice to multidisciplinary teams, as well as CMC technical functions on CMC/Quality regulations and guidelines according to the Agencies expectations for successful approvals. /li liProvide significant contribution or leading efforts for the authoring of CMC documents for the submission to Health Authorities (HA), including MAA preparation, post‑approval variations and responses to HA questions, as well as IMPDs for products under development. /li liCoordinate any CMC regulatory activity required to expand the company portfolio in different territories (e.g. LATAM, APAC, EMA), in close collaboration with internal stakeholders (International Pharma Sales, affiliates, CMO management, etc.) as well as partners and potential vendors. /li liCollaborate in the assessment of Business Development opportunities in relation to CMC topics. /li liEnsure compliance with global regulatory requirements and contribute to the development of internal general standard operating procedures and guidance documents as needed. /li liEstablish good collaboration and interactions across various functions and teams,



such as manufacturing sites (CMOs), Quality Assurance, supply chain, etc. /li liEnsure to be up to date with CMC regulatory intelligence relevant to the company portfolio and pipeline. /li /ul h3Requirements, Skills, and Qualifications /h3 ul liBachelor’s degree in Life Sciences or a related field. /li liFluency in English for business communication. /li liMinimum 5 years in Regulatory CMC field for pharmaceutical products, ideally at a global level. /li liStrong scientific and technical CMC knowledge, along with strategic regulatory mindset. Good knowledge of international CMC regulatory legislation. /li liProven track record of effective collaboration with CMOs, partners and Health Authorities in gaining regulatory approvals and managing life cycle of approved products in different geographical areas. /li liDemonstrable submission history experience for EU and other international territories. /li liKnowledge of regulatory frameworks for medical devices and food supplements desirable. /li /ul h3Seniority level /h3 ul liAssociate /li /ul h3Employment type /h3 ul liFull‑time /li /ul h3Job function /h3 ul liScience, Research, and Project Management /li /ul h3Industries /h3 ul liPharmaceutical Manufacturing, Biotechnology Research, and Business Consulting and Services /li /ul pLocation: Greater Barcelona Metropolitan Area /p /p #J-18808-Ljbffr

📌 Regulatory Affairs Manager CMC (Barcelona)
🏢 Oxford Global Resources
📍 Barcelona