Sr Scientist

Job Summary Responsible for technical evaluation of extractable and leachable studies to ensure that acceptable data is generated to support FDA drug applications. This role will be responsible for providing technical training to other scientists and will serve as a subject matter expert for mass spectrometry and extractable and leachable. This position is located in our Innovation and Development Center in Melrose Park, IL.

Salary Range: $95, Position is eligible to participate in a bonus plan with a target of 6% of the base salary Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities. Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most.

Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.

Requirements Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biological Sciences with 5+ years of related experience or a master’s degree in Pharmaceutical Sciences, Chemistry, Biological Sciences with 3+years of related experience or a PhD in Pharmaceutical Sciences, Chemistry, Biological Sciences, Chemical/Biomedical Engineering with one to three years of related experience is required. In-depth knowledge of Analytical Chemistry or Pharmaceutical Science and various Mass spectrometers is required.

The ability to apply chemistry knowledge for problem-solving and innovative approaches in Method development, Method Validation, and analytical testing is required. Prior knowledge and work experience in extractable, leachable, and impurity identification is a plus. Knowledge and Hands‑on experience in various mass spectrometric operations, troubleshooting, and reporting tools are required. A candidate with experience in any one of Agilent’s HS‑GC/MS, GC‑MS, LC/MS, and ICP/MS instruments to aid in data interpretation of chemical characterization of E&L compounds and for method qualification/validation under a cGMP environment is highly preferable.

Knowledge and experience in mass spectral interpretation and unknown compound identification. Clear understanding of FDA and other regulatory expectations concerning extractable and leachable (e.g., relevant ISO, USP, EP, JP, 21 CFR sections, and industry standards is preferable Candidate should be able to manage multiple projects and new scientific initiatives simultaneously, independently, with others, and as part of a team. Expected to execute all E&L projects with detail and discipline and achieve all project milestones on time.

Expected to lead E/L project activities with minimum guidance and supervision. Able to train junior scientists and strongly desire to learn and contribute to the company's business…