QC Chemist I - Raw Materials

1d1 day ago

Grand River Aseptic Manufacturing

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

About this role

The QC Chemist I supports quality systems for manufacturing and testing cGMP drug products, providing general laboratory support for raw materials and excipient testing. This role suits those exhibiting agility, impact, and methodology in fast-paced environments. Join Grand River Aseptic Manufacturing's community of dedicated individuals improving lives daily.

Daily duties involve performing physical, chemical, and instrumental analyses on active pharmaceutical ingredients, excipients, and finished products. Prepare standards and samples, then run instrumentation like HPLC, FTIR, UV VIS independently per client procedures and SOPs. Ensure compliance with cGMPs, company SOPs, and industry practices throughout all tasks.

Work in a high-standards setting where adaptability and disciplined science ensure excellence, safety, and integrity. Thrive among others driven to make meaningful impact through work, support, and community commitment. Review data for accuracy, clarity, and regulatory adherence while processing and evaluating results.

Grow in an environment offering immediate benefits access and paid volunteerism starting day one. Accrue generous PTO and wellness time off for personal needs. Full job description available during formal interview process.

Requirements

Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology)
Minimum of 1-3 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 active pharmaceutical ingredients, excipients, and finished pharmaceutical products
Prepare standards and samples for analysis
Run instrumentation independently including HPLC, 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 PTO per year for full-time employees, prorated first year
Wellness Time Off: 1 hour earned for every 30 hours worked