Research Associate II, Analytical Sciences (Contract)
- Perform sample analysis using general laboratory techniques, such as weighing, pipetting, and operating laboratory instruments (HPLC, LC-MS, GC, UV-Vis, KF, dissolution apparatus, etc.).
- Execute analysis with a solid understanding of the test procedures, underlying science and proper instrument operation, ensuring accurate and reliable results.
- Utilize available software to control instruments, collect data, process and calculate results, and prepare comprehensive reports.
- Maintain precise and comprehensive records of all analyses in a lab notebook, ensuring compliance with company standards and promoting traceability and consistency in data reporting.
- Prepare test solutions, reagents, and samples for analysis, ensuring accuracy and strict adherence to written instructions and procedures.
- Prepare presentation materials and clearly communicate research results to manager, and at internal/external meetings.
- Work cross-functionally with Process Chemistry and Formulation Development colleagues.
- Requires a B.Sc. degree in chemistry with a minimum of 3 years of relevant research experience, or a M.Sc. degree with at least 1 year of hands-on pharmaceutical/biotech industry experience, or equivalent, in the field of new drug discovery and development.
- Hands-on experience with laboratory techniques, including chromatography (e.g., HPLC, GC, LC/MS), spectroscopy (e.g., UV-Vis, FTIR), titration methods (e.g., Karl Fischer, acid-base), dissolution testing, particle size analysis (by laser diffraction), microscopy, and other compendial methods.
- Experience using laboratory software to collect, analyze, and report data. This might include instrument control software (Chemstation, Empower, etc.) or data analysis programs (Excel, etc.).
- Demonstrated ability to take initiative, ownership, problem identification, problem solving and input into experimental design aspects.
- A proven record of sustained laboratory achievement and innovation.
- Familiarity with industry guidelines such as ICH guidelines, USP requirements, FDA guidance, and good laboratory practices (GLP).
- Exceptional safety and organizational skills and attention to detail when handling samples, recording data, and preparing reports.
- Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment.
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