Trabajo de Pharmaceutical Specialist en Galicia

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. ¿Es este su próximo empleo? Descúbralo leyendo la descripción completa a continuación y no dude en enviar su candidatura. We are looking for someone who can autonomously carry on the work within the scope of their...

Descripción del trabajo In a few words: ¿Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuación. Position: SAP MM Specialist Location: Madrid INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide...

Actual Talent is the talent acquisition consultancy that offers Executive Search, RPO and Talent Solutions. Our purpose is to drive the growth and fulfillment of individuals and organizations. We facilitate individuals in finding inspiring opportunities and help organizations discover professionals who will take them to the next level. We do this through talent acquisition and development...

We are looking for a Senior Regulatory Affairs Specialist to join our regulatory team either in France (Eybens) or Spain (San Agustin Del Guadalix). You will be responsible for ensuring the regulatory compliance of products and services for assigned countries and maintaining alignment with authorities, customers, and internal stakeholders. You will contribute to strategic regulatory analysis,...

A global medical technology company is seeking a Regulatory Affairs professional in San Agustín del Guadalix, Spain. The role focuses on aligning regulatory strategies with business objectives, preparing registration dossiers, and ensuring compliance with local and global regulations. Candidates should have a scientific background and 3-5 years of experience in Regulatory Affairs within the...

Overview Job Description Summary Being a key strategic partner for the EMEA BD Business by (i) supporting the implementation of registration/regulatory strategies for the UCC-SRG portfolios, closely aligned with the region's commercial objectives, to meet EMEA market requirements and (ii) securing local markets by maintaining local licenses compliant with changes related to local/global...

Role Overview My client is a CRO that supports pharmaceutical development from early preclinical phases through late-stage clinical research, supporting the development of the next generation of therapeutics. The principal scientist will provide high-level scientific and technical leadership across bioanalytical activities, with a focus on LC/MS/MS method development, validation and project...

Scientist – Biopharma (Small & Large Molecules) Location: Barcelona area, Spain Shift: Morning shift only (06:00–14:00) Overview A well‐established CRO operating within a GMP/GLP environment is expanding its biopharma team and seeking a Scientist to support technology transfer and validation activities across both small and large molecule products. This role offers broad analytical exposure...

Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimised to improve operational efficiencies, whilst maintaining compliance. Es posible que un gran número de candidatos se presenten a este puesto, así que asegúrese de enviar su CV y su...

Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated technology to provide higher quality and faster access to results. We are...

A global medical technology company is seeking a Regulatory Affairs professional in San Agustín del Guadalix, Spain. The role focuses on aligning regulatory strategies with business objectives, preparing registration dossiers, and ensuring compliance with local and global regulations. Candidates should have a scientific background and 3-5 years of experience in Regulatory Affairs within the...

Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance.Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions...

Overview Job Description Summary Being a key strategic partner for the EMEA BD Business by (i) supporting the implementation of registration/regulatory strategies for the UCC-SRG portfolios, closely aligned with the region's commercial objectives, to meet EMEA market requirements and (ii) securing local markets by maintaining local licenses compliant with changes related to local/global...

Quality Control (QC) Technician – Biologics - Morning Shift 6am-2pm We are seeking a highly motivated and detail-oriented Quality Control Technician to join our team, specializing in the analysis of biological products. This role involves hands-on laboratory work, project management, and technical oversight in a GMP-regulated environment. Key Responsibilities: Design, supervise, and execute...