ASPHALION | Madrid, Community of Madrid, es | 2026-04-28 -
CMC support during drug development, including roadmaps, gap analysis and writing of CMC sections of IMPDs and INDs. CMC in Regulatory Affairs in the Pharmaceutical Industry and/or Consultancy is required. Regulatory Affairs Consultant / Senior Consultant to join our CMC unit of consultants for the - ASPHALION
Italfarmaco España | Madrid, Community of Madrid, es | 2026-05-11 -
Ensure regulatory compliance of CMC sections for global products and drug substances throughout the product lifecycle. Prepare and/or publish eCTD sequences related to CMC content. At least 4 years’ experience in CMC. - Italfarmaco España
ASPHALION | Madrid, Community of Madrid, es | 2026-05-11 -
CMC support during drug development, including roadmaps, gap analysis and writing of CMC sections of IMPDs and INDs. RA CMC liaison with clinical and non-clinical teams, RA lifecycle management teams, technical/subject matter experts, QA, QC, production and supply, as per project needs. Independent - ASPHALION
Randstad España | Madrid, Community of Madrid, es | 2026-05-11 -
The Senior Global CMC Regulatory Affairs professional is a critical strategic role responsible for defining, developing, and executing the global regulatory strategy for the Chemistry, Manufacturing, and Controls (CMC) aspects of assigned pharmaceutical or biological products throughout their lifecy - Randstad España
ASPHALION | Madrid, Community of Madrid, es | 2026-05-11 -
CMC support during drug development, including roadmaps, gap analysis and writing of CMC sections of IMPDs and INDs. Regulatory Affairs Consultant / Senior Consultant to join our CMC unit of consultants for the pharmaceutical industry ! Someone who loves to take on new challenges, to work in an inte - ASPHALION
Italfarmaco España | Madrid, Community of Madrid, es | 2026-04-27 -
Authoring of CMC sections (Drug Product and/or Drug Substance) for new registration applications in CTD format, in alignment with global regulatory strategies and current regulatory guidelines. Authoring and reviewing CMC documentation to support variations and commitments resulting from interaction - Italfarmaco España
LinkedIn | Madrid, Community of Madrid, es | 2026-05-11 -
CMC support during drug development, including roadmaps, gap analysis and writing of CMC sections of IMPDs and INDs. Main responsibilities:
CMC writing of product specific dossiers (Mod. RA CMC change control evaluation/management, when necessary. - LinkedIn
ASPHALION | Madrid, Community of Madrid, es | 2026-05-11 -
Asphalion is growing and we are looking for a Regulatory Affairs Consultant / Senior Consultant to join our CMC unit of consultants for the pharmaceutical industry ! Someone who loves to take on new challenges, to work in an international environment and who wants to grow with us! Main responsibilit - ASPHALION
Italfarmaco España | Madrid, Community of Madrid, es | 2026-05-11 -
Ensure regulatory compliance of CMC sections for global products and drug substances throughout the product lifecycle. Prepare and/or publish eCTD sequences related to CMC content. At least 4 years’ experience in CMC. - Italfarmaco España
ASPHALION | Madrid, Community of Madrid, es | 2026-05-11 -
CMC support during drug development, including roadmaps, gap analysis and writing of CMC sections of IMPDs and INDs. Preparation and participation as a speaker in internal and external team related training sessions focused on CMC of biologics. CMC in Regulatory Affairs in the Pharmaceutical Industr - ASPHALION
Italfarmaco España | Madrid, Community of Madrid, es | 2026-05-11 -
Ensure regulatory compliance of CMC sections for global products and drug substances throughout the product lifecycle. Prepare and/or publish eCTD sequences related to CMC content. At least 4 years’ experience in CMC. - Italfarmaco España
ASPHALION | Madrid, Community of Madrid, es | 2026-05-01 -
CMC support during drug development, including roadmaps, gap analysis and writing of CMC sections of IMPDs and INDs. RA CMC liaison with clinical and non-clinical teams, RA lifecycle management teams, technical/subject matter experts, QA, QC, production and supply, as per project needs. Independent - ASPHALION
Randstad España | Madrid, Community of Madrid, es | 2026-05-11 -
The Senior Global CMC Regulatory Affairs professional is a critical strategic role responsible for defining, developing, and executing the global regulatory strategy for the Chemistry, Manufacturing, and Controls (CMC) aspects of assigned pharmaceutical or biological products throughout their lifecy - Randstad España
ASPHALION | Madrid, Community of Madrid, es | 2026-05-11 -
CMC support during drug development, including roadmaps, gap analysis and writing of CMC sections of IMPDs and INDs. Establishment and improvement of CMC related processes and work instructions. Preparation and participation as a speaker in internal and external team related training sessions focuse - ASPHALION
Randstad España | Madrid, Community of Madrid, es | 2026-05-11 -
The Senior Global CMC Regulatory Affairs professional is a critical strategic role responsible for defining, developing, and executing the global regulatory strategy for the Chemistry, Manufacturing, and Controls (CMC) aspects of assigned pharmaceutical or biological products throughout their lifecy - Randstad España
