CMC Biopharma Regulatory Consultant - Ecolab Life Sciences In this role you apply deep technical expertise in chromatography and biopharma purification to support adoption of Ecolab’s resin and purification solutions.

You work across commercial, regulatory, R&D;, and field teams to translate customer needs into value, driving resin conversions and process improvements.

You’ll engage with customers on methodology, validation, and regulatory strategies while helping de-risk change and ensure quality and supply security.

This position offers a chance to shape Biopharma purification programs at scale in Europe and beyond. * Provide customer-facing technical consulting on downstream purification and resin performance * Act as pre-sales expert to support Biopharma opportunities with resin conversion and process optimization * Collaborate with customers at their sites to improve purification performance, product quality, and efficiency * Advise on resin evaluation, comparability, validation activities and regulatory filing strategy * Contribute to customer change control by delivering technical documentation and risk assessments * Build relationships with Process Development, MSAT, Manufacturing, Quality, Regulatory Affairs, Procurement, and CDMOs * Articulate value of purification solutions focusing on total cost of ownership and regulatory de-risking * Represent the company at meetings,



forums, webinars, and conferences to strengthen credibility * Support product, service, and digital innovation by capturing customer pain points and partnering on scalable offerings * Bachelor of Science degree or equivalent 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, especially chromatography in biologics manufacturing * Experience troubleshooting, investigations, data analysis, and implementing corrective actions * Experience designing and delivering technical training or customer-facing presentations * Strong GMP knowledge, change control, validation principles, and regulatory expectations for Biopharma * Excellent communication, analytical thinking, customer discovery, problem solving, and stakeholder influencing skills * Ability to travel 50%+ regionally and globally; valid driver’s license; travel visas as needed In this role you apply deep technical expertise in chromatography and biopharma purification to support adoption of Ecolab’s resin and purif… #J-18808-Ljbffr

📌 CMC Biopharma Regulatory Consultant - Ecolab Life Sciences (Italia)
🏢 Experteer Italy
📍 Italia