Senior Pharmacovigilance Specialist - Catalonia - beBeeRegulador

The Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products. · ...

We are seeking a highly motivated and detail-oriented Quality Control Technician to join our team. · Bachelor's or Master's degree in Biochemistry, Biotechnology, Chemistry, or a related field. · Minimum of 3 years of hands-on experience with HPLC and chromatography techniques. · ...

A well‑established CRO is expanding its biopharma team and seeking a Scientist to support technology transfer and validation activities across small and large molecule products.,This role offers broad analytical exposure within a regulated setting. · , Candidates currently workin ...

Job summary · Scientist – Biologics & Advanced Therapies (Quality Control) · This role focuses on analytical method development and validation for complex biologics, including monoclonal antibodies, recombinant proteins, and advanced therapy products. · ...

A growing clinical research organization in Barcelona is seeking a Research Nurse with experience in decentralized or hybrid clinical trial models. · This role blends traditional on‑site clinical activities with remote patient support, digital health tools, and home‑based procedu ...

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. · ...

Performs all aspects of the collection, processing and reporting of adverse events adhering to all data protection guidelines. · ...

+The Associate Director will lead medical affairs strategy for renal diseases globally. · +Develops/owns Integrated Evidence Plan (IEP) for current and pipeline indications. · Provides input into development while ensuring US and Int'l medical perspective is reflected. · Liaises ...

The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs.Focused on innovative evidence and launch readiness along with post-market solutions, including medical affairs planning and execution of ...

The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs. Focused on innovative evidence and launch readiness along with post-market solutions including medical affairs planning and execution of ...

This Senior Safety Project Lead position is responsible for managing and delivering excellence in assigned projects covering Lifecycle Safety functions. The role involves leadership and accountability for customer-facing activities and operational service delivery. · ...

We are hiring Quality Assurance Specialist in Barcelona. Neuraxpharm is looking for people who want to make a difference and improve patients' lives. The mission is to provide an effective quality assurance system that ensures compliance with Good Manufacturing Practice as part o ...

We want individuals who will go the extra mile and make great things happen. · We are guided by a Diversity & Inclusion policy to ensure a business culture based on the principles of diversity, equality and inclusion. · ...

GP Pharm busca un/a QA Specialist en Farmacovigilancia con experiencia en Garantía de Calidad (QA) aplicada en entornos GxP. La misión principal es mantener y supervisar el Sistema de Calidad de Farmacovigilancia y dar soporte documental. · ...

GP Pharm está buscando a un/a QA Specialist para su equipo en Farmacovigilancia. · ...

Buscamos un/a Especialista en Farmacovigilancia para mantener y supervisar nuestro Sistema de Calidad. · ...