Scientist / Sr Scientist, Process Development

Role OverviewWe are seeking a highly motivated and experienced Scientist / Sr. Scientist to join our Process Development team. In this role, you will serve as a hands-on technical expert for purifying and characterizing bispecific and multi-specific antibodies to advance the company’s pipeline. The ideal candidate combines deep practical expertise in downstream process development and analytical characterization with the ability to partner closely with CDMOs to bridge internal development to external manufacturing.Key ResponsibilitiesDesign, execute and drive fit-for-purpose and scale-up purification processes (e.g. Protein A, IEX, SEC etc.) for antibodies and complex biologic formats.Evaluate product quality attributes including purity, aggregation, charge heterogeneity and binding activity with a broad range of analytical techniques (e.g. SEC-HPLC, SDS-PAGE, icIEF, Octet, BLI/SPR, MS etc.) Serve as technical liaison with CDMO partners — prepare technology transfer materials and support manufacturing runs from a technical standpoint.Author and review SOPs, technical reports, development summaries, and regulatory documents (IND/IMPD, BLA/MAA modules).Contribute to cross-functional discussions and help shape development strategy with a lean teamRequired QualificationsEducation & ExperienceBachelor’s, Master’s, or PhD in Biochemistry, Bioengineering, Molecular Biology, or related field with 2-12 years of industry biologics process development experience. Hands-on experience with antibody purification, and protein characterization — this is a bench-active role. Experience with multispecific antibody formats (bispecifics or similar).Skills & MindsetComfortable working independently and navigating ambiguity in an early-stage environment with evolving priorities.Experience working with or managing CDMOs on technical issues, including tech transfer and troubleshooting.Strong communicator who can translate bench findings into clear summaries for cross-functional teams.Familiarity with IND-enabling development and basic GMP awareness; deep regulatory expertise not required.Startup mentality — resourceful, collaborative, and willing to roll up your sleeves.