QC Chemist II

3d3 days ago

Grand River Aseptic Manufacturing

Grand Rapids, US · Full-time

About this role

The QC Chemist II supports quality systems as they relate to the manufacturing and testing of cGMP drug products. This role provides general laboratory support for in-process, stability, and finished product testing. A disciplined, science-based approach ensures consistent excellence, safety, and integrity in all work.

Perform physical, chemical, and instrumental analysis of pharmaceutical products according to client and compendia procedures. Prepare standards and samples, then independently operate HPLC, GC, FTIR, UV VIS, and physical testing equipment. Process data, generate reports, and evaluate results while maintaining accurate records.

Work in a fast-paced environment that values agility, adaptability, and high standards. Review laboratory data for accuracy, clarity, and adherence to GMP and GLP regulations. All responsibilities are carried out in compliance with cGMPs, company SOPs, and current industry practice.

Contribute to meaningful impact through support of drug product quality and community volunteerism. The position offers opportunities to learn new techniques and perform multiple tasks simultaneously while following instructions and company policies.

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; Ability to communicate effectively with management, staff, and regulatory agencies by exhibiting excellent interpersonal skills.
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 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.

Benefits

Medical, prescription, dental, vision, life insurance, and disability benefits available on first day with company paying a portion of the cost.
401(k) program with all contributions immediately 100% vested.
16 hours of paid volunteer time per calendar year.
PTO accrual up to 104 hours per calendar year plus wellness time off earned at 1 hour per 30 hours worked.
10 paid holidays per calendar year with immediate eligibility.
Generous off-shift premiums.