QC Chemist II

21h21 hours ago

Grand River Aseptic Manufacturing

Grand Rapids, US · Full-time · $75,000 – $95,000

About this role

Grand River Aseptic Manufacturing seeks a QC Chemist II who exhibits agility, impact, and methodology. Thrive in fast-paced environments where adaptability and high standards ensure excellence, safety, and integrity. Join a community of dedicated individuals improving lives through cGMP drug product manufacturing and testing.

The QC Chemist II supports quality systems for in-process, stability, and finished product testing. Perform physical, chemical, and instrumental analyses on pharmaceutical products. Operate instrumentation like HPLC, GC, FTIR, UV VIS independently per client procedures and SOPs.

Work on 1st shift Group B: Wednesday through Saturday, 6:00 am to 4:00 pm. Review data for accuracy, clarity, and GMP/GLP compliance. Process data, generate reports, and evaluate results while complying with cGMPs and company SOPs.

Gram offers benefits starting day 1, including medical, dental, vision, and 401(k) with immediate vesting. Earn paid time off, wellness time, and volunteer hours. Enjoy 10 paid holidays and generous off-shift premiums in a supportive environment.

Requirements

Bachelor’s degree in Chemistry and/or other 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 skills with ability to communicate effectively with management, staff, and regulatory agencies
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Responsibilities

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 available starting day 1, with company paying a portion of the cost
401(k) contributions immediately 100% vested for employee and company contributions
Generous off-shift premiums
16 hours of paid volunteer time per calendar year starting day 1
Up to 104 hours of paid time off per calendar year for full-time employees
Wellness time off: 1 hour for every 30 hours worked
10 paid holidays per calendar year