Responsibilities
- Develop and validate reverse phase and chiral HPLC methods to support purity evaluation and characterization of both GMP and non-GMP radio-labelled active pharmaceutical ingredients.
- Promptly identify and resolve issues related to HPLC instrumentation and method performance.
- Generate accurate and reliable analytical data in accordance with documented procedures, client requirements, and project timelines.
- Provide regular updates on project progress and escalate technical or operational challenges to supervisors, project teams, and clients as needed.
- Act as a representative of the analytical team and the organization in internal project meetings and external client discussions.
- Independently organize and prioritize work with limited oversight.
- Address and resolve advanced scientific and analytical challenges.
- Manage multiple concurrent projects while maintaining accuracy and adherence to protocols.
- Lead investigations into out-of-specification results and oversee the creation of related quality documentation.
- Support compliance with regulatory standards by promoting sound scientific practices and suggesting process enhancements.
- Show potential or experience in guiding and supporting less experienced laboratory scientists.
Benefits
- Comprehensive and competitive total rewards program
Compensation
Not specified
Work Arrangement
Not specified
Team
Not specified
Training
Training will be provided for the right candidate.
Supervision
Must be able to work with minimal supervision.
Project Management
Must be able to work on multiple projects simultaneously.
Not specified
