Overview
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In this role you will lead analytical development activities for new chemical entities and solid dosage forms, guiding a multidisciplinary team to drive method development, validation, transfer, and regulatory-compliant delivery across preclinical to Phase III programs. You will align analytical strategy with development objectives, ensure quality and regulatory readiness, and partner with cross-functional teams to enable successful submissions. The role combines scientific leadership with hands-on expertise to shape development programs and lifecycle management. You will be pivotal in applying QbD principles and ensuring robust, compliant analytics that support global regulatory filings.
Compensaciones / Incentivos
flexible working model
volunteering activities
development & learning opportunities
remuneration and benefit customization
physical, emotional and financial wellbeing support
Responsabilidades
Lead and develop the Analytical Development team, fostering excellence and continuous improvement
Steer analytical drug development across all stages (method development, validation, transfer) for multiple programs
Plan, prioritize, and allocate resources to ensure timely delivery and project alignment
Provide hands-on expertise in analytical methods (HPLC, UHPLC, LC-MS/MS, GC, UV-Vis, FTIR) and physicochemical characterization (XRPD, DSC,



TGA, DVS, particle size, microscopy, Karl Fischer)
Ensure regulatory compliance (ICH Q14, Q2(R2), Q8, Q9; GMP and data integrity) and support lifecycle management and QA
Promote Quality by Design and analytical lifecycle thinking (ATP, risk assessment, robustness, transfer)
Draft, review and approve Analytical Development documentation; support regulatory submissions (EU/US) and dossier input
Collaborate with Regulatory Affairs, Quality, Manufacturing, Formulation Development and external stakeholders
Maintain laboratory facilities and equipment, ensuring qualification, calibration, and training
Engage in cross-functional interactions to enable successful development and project execution
Requisitos xqbhyrx principales
Advanced degree in Pharmaceutical Sciences, Chemistry, Analytical Chemistry or related scientific discipline
Extensive Analytical Development experience in the pharmaceutical industry (early to late development)
Proven leadership of scientific teams in Analytical or Pharmaceutical Development
Strong background in development of solid oral dosage forms; experience with liquids, suspensions, or injectables valued
Solid understanding of GMP and regulatory requirements; experience with EMA, FDA interactions and submissions
Experience working in cross-functional teams and managing multiple development programs
Empathy
Humility
Curiosity
HPLC
UHPLC
LC-MS/MS

📌 SENIOR ANALYTICAL DEVELOPMENT MANAGER (Barcelona)
🏢 Ferrer
📍 Barcelona