Scientist 1, Analytical Chemist

MillenniumSoft Inc; Vernon Hills (IL); On-site; USD 70,000 - 79,000; Part time

Job summary

MillenniumSoft Inc. in Vernon Hills, IL, is seeking an entry-level Scientist 1, Analytical Chemist for a 12-month contract. The role is 1st shift, 40 hours per week, with pay rate $35.79/hr.

The assignment covers analytical chemistry support for client products and new development, plus method development and validation. Responsibilities include testing, data entry, protocol/report generation, and collaboration with Regulatory, Manufacturing, and Quality teams.

Qualifications

• BS/MS in Chemistry, Pharmaceutics, or related science field required.
• Ability to interact cross-functionally with Regulatory, Manufacturing, and Quality teams.

Responsibilities

• Perform chemistry and performance testing
• Conduct data review and entry
• Generate protocols and reports
• Provide laboratory maintenance and support
• Support stability testing for design change approvals
• Develop and validate analytical methodologies for materials and products
• Discuss results with Regulatory and Quality teams

Skills

HPLC

GC

UV-Vis

Titration

pH testing

Analytical methods

Scientific writing

GMP documentation

FDA compliance

Data review

Education

BS in Chemistry

MS in Chemistry

Pharmaceutics background

Job description

Position : Scientist 1,Analytical Chemist

Location : Vernon Hills, IL

Duration : 12 Months

Total Hours/week : 40.00

1st Shift

Client : Medical Devices Company

Job Category : Clinical

Level of Experience : Entry Level

Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)

Note

Pay rate $35.79/hr

Working Hours: Monday-Saturday, 9:00 AM to 5:00 PM

Job Summary

Provides analytical chemistry support and/or remediation for chemistry-related projects related to Client products currently on the market, as well as new product development. Participates in stability testing programs supporting approval of process/product design changes and supports development/validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.

Roles & Responsibilities

• Perform chemistry and performance testing
• Conduct data review and entry
• Generate protocols and reports
• Provide laboratory maintenance and support
• Support stability testing programs for process/product design change approvals
• Develop and validate analytical methodologies for raw materials, in-process, and finished product release testing
• Discuss scientific strategies/results and interact with other functional areas (Regulatory, Manufacturing, Quality)

Experience

• 2-4 years of experience in pharmaceutical analytical chemistry (essential)
• Hands-on experience with wet-chemistry and instrumental techniques (pH, titration, UV-Vis, GC, HPLC)
• Experience working within an FDA-regulated environment and GMP documentation requirements
• Previous experience writing scientific protocols and reports

Key Skills

• Standard scientific method and techniques within respective discipline
• Excellent scientific writing skills
• Multi-tasking across various activities
• Troubleshooting and problem-solving
• Interpreting instructions in written, oral, diagram, or schedule form

Eligibility & Qualifications

• BS/MS in Chemistry, Pharmaceutics, or related science field required
• Ability to interact cross-functionally with Regulatory, Manufacturing, and Quality teams