Senior CMC Regulatory Affairs Specialist

A leading consulting firm in Barcelona seeks a dedicated Senior CMC RA Specialist. This on-site role focuses on ensuring regulatory compliance in Chemistry, Manufacturing, and Controls (CMC) documentation. The ideal candidate has over 10 years of experience in Regulatory Affairs within the pharmaceutical industry, strong knowledge of GMP and ICH guidelines,...

Regulatory Affairs Associate (Medicines) Company: Inter RegulatoryEmployment Type: Full-timeAbout the role Inter Regulatory is expanding its European Regulatory Affairs team and is seeking a Regulatory Affairs Associate (Medicines) to join our consultancy based in Barcelona , primarily working from the Barcelona Health Hub .This role is suited to a...

Regulatory Affairs Associate (Medicines)Location:Barcelona, Spain (Hybrid – Barcelona Health Hub)Company:Inter RegulatoryEmployment Type:Full-timeAbout the roleInter Regulatory is expanding its European Regulatory Affairs team and is seeking aRegulatory Affairs Associate (Medicines)to join our consultancy based inBarcelona, primarily working from...

**Location: Barcelona, Spain (we requiere 3 days working from the office and 2 days working from home** Our **Chemistry, Manufacturing, and Controls (CMC) Regulatory Affairs** function delivers expert CMC regulatory input for projects spanning across the product lifecycle and leads the regulatory strategy for the development, manufacturing and testing of...

A growing regulatory consultancy in Barcelona is seeking a Regulatory Affairs Associate with 3-5 years of experience in pharmaceutical Regulatory Affairs. The role involves authoring and managing regulatory dossiers, handling CMC documentation, and supporting US regulatory applications. Candidates should have a scientific degree and be fluent in English and...

Join to apply for the CMC RA Senior Specialist - Barcelona role at Project Delivery Partners . Position Title: CMC RA Senior Specialist - Barcelona Location: BarcelonaType of Contract: Full-Time / On site PharmEng Technology, an Efor Group of Companies, is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative...

Position Title: CMC RA Senior Specialist - Barcelona Location: Barcelona Type of Contract: Full-Time / On site PharmEng Technology, an Efor Group of Companies, is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to...

Oxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company to support headquartered in Barcelona through our consulting services division.Key Responsibilities:Provide CMC regulatory insight and advice to multidisciplinary teams, as well as CMC...

Oxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company to support headquartered in Barcelona through our consulting services division. Key Responsibilities: Provide CMC regulatory insight and advice to multidisciplinary teams, as well as CMC...

Oxford Global Resources is seeking a Global CMC Regulatory Affairs Manager Consultant to support as external contractor on behalf of Oxford a top leading pharma company to support headquartered in Barcelona through our consulting services division.Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta...