Scientist - ADC DMPK Aurigene Oncology Limited

  • company name Aurigene Oncology Limited
  • working location Office Location
  • job type Full Time

Experience: 2 - 2 years required

Pay:

Salary Information not included

Type: Full Time

Location: Karnataka

Skills: pharmacology, biochemistry, Bioanalysis, ELISA, Bioinformatics, DMPK, toxicology, Communication, Innovation, Team Leadership, Pharmaceutical Analysis, Pharmaceutical Chemistry, large molecule, ADC PK, Antibody Drug Conjugate characterisation, mass spectrometryHRMS, QTOF, Triple quad, LCMSMS, MSD, BioPharma Finder, MaxQuant, Spectronaut, PKPD, translational sciences

About Aurigene Oncology Limited

Job Description

Desired Profile: M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry) with 11-14 years or Ph.D. with 2-5 years experience in large molecule/ADC PK and bioanalysis, Antibody Drug Conjugate characterisation and bioanalysis, mass spectrometry-HRMS, Q-TOF & Triple quad Roles & Responsibilities: Expert in designing and executing DMPK studies to support antibody-drug conjugate (ADC) and monoclonal antibody (mAb) programs, from discovery through IND-enabling stages. Extensive experience in quantification of biologics including antibodies, therapeutic proteins, ADCs, and peptides using LC-MS/MS, MSD, and ELISA platforms. Proficient in advanced bioinformatics tools such as BioPharma Finder, MaxQuant, Spectronaut, and other relevant analytical software. Skilled in applying innovative techniques for function-based identification and selection of ADC and mAb lead candidates, with a strong focus on DMPK profiling to ensure safe and effective therapeutic development. Experienced in interpreting complex DMPK data and providing actionable insights to cross-functional project teams. Actively represent DMPK functions in internal and external meetings, fostering collaboration and strategic alignment. Collaborate closely with cross-functional departments to address ADC-related challenges and deliver integrated solutions from target validation to IND submission. Accountable for authoring and reviewing SOPs, study protocols, reports, and regulatory documentation to support both GLP and non-GLP studies. Strong foundational knowledge of DMPK principles, including PK/PD, toxicology, and translational sciences. Demonstrated capabilities in communication, innovation, and team leadership.,