QC Chemist II — Fast-Paced Pharma Quality, Day-1 Benefits

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Benefits from day 1

401(k) vesting

Paid volunteer time

Paid time off

Wellness time off

Paid holidays

Competitive pay

Job summary

Grand River Aseptic Manufacturing (GRAM) seeks a QC Chemist II in Grand Rapids, MI to support quality systems for the manufacturing and testing of cGMP drug products, including in-process, stability, and finished product testing.

You will perform physical, chemical, and instrumental analyses, prepare standards, run instrumentation such as HPLC, GC, FTIR, UV/Vis, review laboratory data for GMP/GLP compliance, and generate reports.

Qualifications

• Bachelor’s degree in Chemistry and/or other related discipline.
• Minimum of 3 years pharmaceutical or testing experience.
• Qualification for use of a full-face respirator is required.
• Proficient computer skills in Microsoft Word, Excel, and Outlook.

Responsibilities

• Perform physical, chemical, and instrumental analysis of in-process and finished pharmaceutical products.
• Prepare standards and samples for analysis.
• Run instrumentation independently including, but not limited to, HPLC, GC, FTIR, UV VIS, and physical testing on pharmaceutical products according to client/compendia procedures and departmental SOPs.
• Review laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
• Process data, generate reports, and evaluate data.
• Perform all job responsibilities in compliance with cGMPs, company SOP’s, and current industry practice.

Skills

Laboratory skills

Attention to detail

Communication skills

Education

Bachelor’s degree in Chemistry

Tools

MS Word

Excel

Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) seeks a QC Chemist II in Grand Rapids, MI to support quality systems for the manufacturing and testing of cGMP drug products, including in-process, stability, and finished product testing.

You will perform physical, chemical, and instrumental analyses, prepare standards, run instrumentation such as HPLC, GC, FTIR, UV/Vis, review laboratory data for GMP/GLP compliance, and generate reports.