Experteer Overview
In this role you will provide expert technical and regulatory consulting to enable the adoption of Ecolab chromatography resin and purification solutions in Biopharma manufacturing. You will work cross-functionally with commercial, regulatory, Ru0026amp;D, and field teams to translate customer challenges into value, support resin conversions, and strengthen Ecolab’s role as a trusted technical partner. Expect to travel regionally and internationally to customer sites and industry forums, shaping purification strategies and regulatory compliance. You’ll drive impact by optimizing downstream processes, validating approaches, and de-risking change across Biopharma programs. This is a hands-on, customer

Compensaciones / Ventajas
• Provide technical consulting on chromatography resin performance and downstream purification
• Support resin evaluation, comparability, and validation activities with experimental design and regulatory filing strategy
• Assist in change control processes with technical documentation, risk assessments, and training materials
• Act as pre-sales technical expert for Biopharma opportunities involving resin conversion and process optimization
• Engage with customers at facilities to identify purification improvements, product quality, efficiency, resin lifetime, and risk mitigation
• Build relationships with Process Development, MSAT, Manufacturing, Quality, Regulatory Affairs,



Procurement, and CDMO stakeholders
• Present at customer meetings, technical forums, and conferences to strengthen credibility in Biopharma purification
• Help shape product, service, and digital offerings by capturing customer pain points and collaborating with cross-functional teams

Responsabilidades
• Bachelor of Science degree in Life Sciences, Biochemistry, Biotechnology, Chemical Engineering, Bioprocess Engineering, or related discipline
• Experience in Biopharma manufacturing, process development, MSAT, purification sciences, technical service, quality, regulatory affairs, or related customer-facing role
• Strong understanding of downstream purification processes and chromatography in biologics manufacturing
• Experience troubleshooting, investigations, data analysis, and implementing corrective actions
• Experience delivering technical training or customer-facing presentations
• Strong knowledge of GMP, quality systems, change control, validation, and regulatory expectations for Biopharma manufacturing
• Excellent communication, analytical thinking, and stakeholder influencing skills
• Ability to travel 50%+ regionally and globally as needed
• Valid driver's license and ability to obtain travel visas
• Fluent in English

Requisitos principales
• comprehensive and market-competitive benefits

📌 CMC Biopharma Regulatory Consultant - Ecolab Life Sciences (Barcelona)
🏢 Ecolab
📍 Barcelona