Analytical Chemistry

Indotronix Avani Group; Vernon Hills (IL); On-site; USD 70,000 - 90,000; Full time

Job summary

Indotronix Avani Group is seeking an analytical chemist to support chemistry-related BD projects, including stability testing for design changes and new product development.

The role also involves developing and validating analytical methods for raw materials, in-process samples, and finished product release testing within an FDA-regulated, GMP environment.

Qualifications

• BS or MS in Chemistry or Pharmaceutics with related science experience.
• 2–4 years’ experience in pharmaceutical analytical chemistry is essential.
• Hands-on experience with wet-chemistry and instrumental techniques (pH, titration, UV-Vis, GC, HPLC).
• Experience in FDA-regulated environment and GMP documentation.

Responsibilities

• Provide analytical chemistry support for BD products on market and new product development.
• Participate in stability testing to support process/product design changes.
• Develop and validate analytical methods for incoming materials, in-process, and finished product testing.

Skills

Wet-chemistry

Instrumental techniques

FDA-regulated environment

Education

BS/MS in Chemistry/Pharmaceutics

Tools

HPLC

GC

UV-Vis

Titration

Job description

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.

Education

• BS/MS in Chemistry / Pharmaceutics with related science experience

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.