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Scientist , Analytical Chemistry Development

Job in Vernon Hills, Lake County, Illinois, 60061, USA
Listing for: MillenniumSoft Inc
Full Time position
Listed on 2026-09-22
Job specializations:
  • Science
    Research Scientist, Pharmaceutical Science/ Research, Analytical Chemist, Chemistry
Salary/Wage Range or Industry Benchmark: 41000 - 58000 USD Yearly USD 41000.00 58000.00 YEAR
Job Description & How to Apply Below
Position: Scientist 1, Analytical Chemistry Development

Job Title:

Scientist 1, Analytical Chemistry
Rate of pay $35.79
On site 5 days

Segment/Department Name:
Infection Prevention, Analytical Chemistry
Purpose Of Position
This position provides analytical chemistry support and/or remediation to all chemistry-related projects for BD products currently on the market as well as new product development. This position will also participate in the conduct of the stability testing program to support the approval of process and/or product design changes. As needed, this position also supports the development and validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.
General Functions, Specific Responsibilities, And Authority
Chemistry & performance testing, data review and entry, protocol/report generation, laboratory maintenance and support.
Knowledge, Education, And Skills Required

  • Education
  • BS/MS in Chemistry / Pharmaceutics with related science experience
  • Skills
  • Demonstrates developed knowledge of respective scientific discipline and standard scientific method and techniques.
  • Excellent scientific writing skills.
  • Ability to multi-task various activities.
  • Troubleshoot issues that arise and solve problems.
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
  • Experience
  • 2-4 years experience in pharmaceutical analytical chemistry is essential.
  • Hands-on experience with wet-chemistry and instrumental techniques (i.e. pH, tritration, UV-Vis, GC, HPLC).
  • Experience in working within an FDA regulated environment and GMP documentation requirements.
  • Specialized Knowledge
  • Ability to discuss scientific strategies/results and interact with other functional areas, including Regulatory, Manufacturing, and Quality.
  • Previous experience with writing scientific protocols and reports.
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