We’re looking for a motivated and curious scientist to support testing and method development in our growing lab team. In this role, you’ll help ensure the quality and safety of our products by performing routine testing and contributing to important lab documentation. If you have a background in the sciences, some hands-on lab experience, and an interest in the biopharma world, this could be a great next step in your career.Key Responsibilities:Conduct routine and complex sample testing in the residual impurity lab within Analytical SciencesAuthor and review Standard Operating Procedures (SOPs) to ensure compliance with regulatory standards and best practicesPerform ELISA and PCR testing for impurity analysis and characterizationAnalyze and interpret complex data sets, preparing comprehensive reports for internal stakeholders and regulatory submissionsCollaborate with cross-functional teams to troubleshoot issues and optimize testing processesParticipate in method validation studies to ensure the accuracy and reliability of analytical proceduresMaintain detailed laboratory notebooks and electronic records in compliance with GMP standardsContribute to the development and optimization of impurity profiles for drug substances and drug productsAssist in the preparation of regulatory documentation related to impurity testing and control strategies
- ID: #53941660
- State: Maryland Gaithersburg 20877 Gaithersburg USA
- City: Gaithersburg
- Salary: USD TBD TBD
- Job type: Full-time
- Showed: 2025-05-29
- Deadline: 2025-07-28
- Category: Et cetera