Sobre Ardena Ardena es una organización global especializada en el desarrollo y fabricación por contrato (CDMO) y en investigación por contrato (CRO), centrada en el desarrollo de medicamentos de precisión. Apoyamos a compañías farmacéuticas y biotecnológicas
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
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
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
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
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
Regulatory Affairs Consultant specializing in CMC for biological products, focusing on dossier preparation, drug development support, and project management within the pharmaceutical industry....
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
KEY RESPONSIBILITIES 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
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
Syneos Health, Inc. is seeking a Regulatory Consultant - CMC for their Madrid location, focused on overseeing and executing multi-product global regulatory strategies for small molecule products. This role involves preparing regulatory CMC documentation and being the primary
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
Senior Regulatory Affairs CMC Specialist We are seeking a highly experienced Regulatory Affairs professional with deep Chemistry, Manufacturing & Controls (CMC) expertise to support global regulatory activities across a diverse and innovative product portfolio. The successful candidate will
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
Regulatory Consultant - CMC (CMC with small molecule products) Updated: Yesterday Location: Madrid, Spain Job ID: -OTHLOC-3529-2DMAD-2DR Description Regulatory Consultant - CMC (CMC with small molecule products) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization
KEY RESPONSIBILITIES 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
In a nutshell Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge