Process Development Scientist
Pubblicato il 03-09-2026 - Biopharma Careers in Milano
ppWork Your Magic with us!
/ph3Your Role /h3pAs a Subject Matter Expert (SME) in Downstream Processing and Single Use Technologies, you will drive innovation and solve complex bioprocessing challenges for our clients.
You will lead hands-on process development, scale-up, and troubleshooting studies, converting raw data into scientific recommendations.
Acting as a technical authority, you will support commercial success through direct customer consultations, strategic partnerships, training programs, and thought leadership activities (webinars, conferences) in collaboration with internal RD and marketing teams /ph3Key Responsibilities /h3ulliAct as the primary SME in Downstream Processing and Single Use Technologies, providing expert guidance on both batch and integrated bioprocesses.
Design and execute hands-on process development, scale-up, and implementation activities following self-developed protocols.
/liliProcess and analyze raw data /liliLead scale-down studies to support troubleshooting, root cause investigations, and process optimization.
/liliWork closely with clients' technical teams, delivering consultative and hands-on guidance.
/liliEngage in and deliver thought leadership activities, including industry conference presentations, seminars, customer trainings, and webinars.
Deliver training programs to both internal and external customers.
/liliCollaborate effectively with internal commercial, RD, and marketing teams to address customer needs,
factor in commercial success expectations, and drive continuous improvement of team capabilities.
/li /ulh3Who You Are /h3ulliYou have an Italian work permit / live in Italy /liliMaster degree or Ph.D.
In Biochemical Engineering or Life Sciences /liliExperience in customer-facing technical roles or scientific consulting.
/liliFamiliarity with scientific modeling tools applied to bioprocess optimization.
/lili5-10 years of experience in delivering technical presentations at industry conferences or seminars.
/liliKnowledge of regulatory frameworks relevant to biopharmaceutical manufacturing (GMP, ICH guidelines).
/liliExperience in Systems and Automation is considered a plus.
/li /ulh3Salary Package /h3ulliAnnual Base Salary (RAL): €****** - €****** /liliVariable Compensation (SIP) /liliWelfare and Benefits Package /li /ulh3What we offer /h3pWe are curious minds that come from a broad range of backgrounds, perspectives, and life experiences.
/ppWe believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology.
/ppWe are committed to creating access and opportunities for all to develop and grow at your own pace.
/ppJoin us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
/p /p #J-*****-Ljbffr