Analytical Scientist

Pay Rate Low: 45 | Pay Rate High: 50 Our client is seeking a highly motivated Anlaytical Scientist to join a growing Pharmaceutical Sciences team focused on advancing innovative cancer therapies. This is an excellent opportunity for a hands‑on scientist who enjoys contributing across multiple projects in a collaborative, fast‑paced environment. What You’ll Do Perform HPLC method development and validation, including troubleshooting and optimization, to support drug development activities. Conduct stability testing in accordance with ICH guidelines, including sample analysis, data interpretation, and documentation. Execute analytical testing on solid oral dosage forms (tablets) using techniques such as HPLC, LC-MS, GC, UV‑Vis, Karl Fischer, and dissolution testing. Perform dissolution testing for tablets and other dosage forms to support formulation development and stability studies. Operate laboratory software to control instruments, collect and analyze data, and generate clear, well‑documented reports. Prepare samples, reagents, standards, and test solutions in strict accordance with SOPs and compendial methods. Maintain accurate, compliant laboratory documentation to ensure data integrity, traceability, and regulatory readiness. Summarize and present analytical results to management and at internal or external meetings. Collaborate closely with cross‑functional partners in Process Chemistry and Formulation Development. What We’re Looking For B.S. in Chemistry with 3+ years of relevant pharmaceutical or biotech experience, or M.S. in Chemistry with 1+ year of industry experience. Strong hands‑on experience with HPLC method development and validation, stability testing, dissolution testing, and analysis of tablet dosage forms. Experience with chromatography, spectroscopy, titration methods, and other compendial analytical techniques. Proficiency with laboratory and data analysis software (e.g., Empower, ChemStation, Excel). Solid understanding of GLP/GMP and industry standards, including ICH, USP, and FDA guidance. Strong problem‑solving skills with the ability to take ownership of analytical work and contribute to experimental design. Excellent attention to detail, organization, and commitment to laboratory safety. Ability to work independently while thriving in a collaborative, multidisciplinary team. #J-18808-Ljbffr Astrix