Senior Scientist I, Analytical Development
Senior Scientist I, Analytical Development
Support analytical development and testing activities conducted at contract organizations (CMOs/CROs), including method development, method qualification/validation, and release/stability testing.
Serve as a technical subject matter expert (SME) for analytical methods, ensuring that outsourced activities meet quality standards and project timelines.
Review and interpret data from method validations, release testing, and characterization studies for drug substance (DS) and drug product (DP).
Prepare, review, and/or approve protocols, reports, and regulatory submission documents (IND, NDA/MAA, IMPD).
Collaborate cross-functionally with Quality, Regulatory, and external partners to ensure analytical alignment with project goals and regulatory expectations.
PhD in Chemistry, Pharmaceutical Sciences, or a related field with a minimum of 5 years of relevant industry experience; or MS with 8+ years of experience in analytical development.
Proficiency in analytical techniques such as HPLC/UPLC, LC-MS, XRPD, dissolution testing, DSC, DVS, and compendial methods (e.g., USP/EP).
Understanding of ICH guidelines (e.g., Q2, Q6A, Q3A,B,C,D, M7), FDA/EMA regulatory expectations, and phase-appropriate analytical development.
Strong data interpretation and problem-solving skills.
Excellent written and verbal communication skills, with the ability to translate complex scientific concepts into clear documentation.
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