QC Chemist II

4w1 month ago

Grand River Aseptic Manufacturing

Grand Rapids, US · Full-time · $55,000 – $75,000

About this role

Grand River Aseptic Manufacturing (GRAM) is seeking a QC Chemist II to support quality systems as they relate to the manufacturing and testing of cGMP drug products. You will provide general laboratory support for in-process, stability, and finished product testing in a fast-paced environment where agility, adaptability, and high standards go hand in hand.

Day-to-day duties include performing physical, chemical, and instrumental analysis of in-process and finished pharmaceutical products. You will prepare standards and samples, run instrumentation independently—including HPLC, GC, FTIR, UV VIS—and process data to generate reports and evaluate results.

The team operates with a disciplined, science-based approach ensuring consistent excellence, safety, and integrity. You will review laboratory data for accuracy and adherence to GMP and GLP regulations, all while complying with company SOPs and current industry practice.

GRAM offers a community of dedicated individuals improving lives every day, with benefits starting on day one and a culture that encourages giving back through paid volunteerism. This role provides an opportunity to grow within a company that values impact and high standards.

Requirements

Bachelor’s degree in Chemistry or related discipline (e.g., Biochemistry, Biotechnology).
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.
Excellent written and verbal communication skills (preferred).
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies (preferred).

Responsibilities

Provide general laboratory support for in-process, stability, and finished product testing.
Perform physical, chemical, and instrumental analysis of in-process and finished pharmaceutical products.
Prepare standards and samples for analysis.
Run instrumentation independently including HPLC, GC, FTIR, UV VIS, and physical testing 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 SOPs, and current industry practice.

Benefits

Medical, prescription, dental, vision, life insurance, and disability benefits starting day 1.
401(k) program with immediate 100% vesting of contributions and GRAM contributions once eligible.
16 hours of paid volunteer time per calendar year.
Paid time off: up to 104 hours per year plus wellness time off (1 hour per 30 hours worked).
10 paid holidays per calendar year with immediate eligibility.