QC Chemist II

4w1 month ago

Grand River Aseptic Manufacturing

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

About this role

Agility, Impact, Methodology. If these values resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to join our community of dedicated individuals improving lives every day. As a QC Chemist II, you will support quality systems relating to the manufacturing and testing of cGMP drug products.

Your day-to-day involves providing general laboratory support for in-process, stability, and finished product testing. You will independently run instrumentation including HPLC, GC, FTIR, UV VIS, and perform physical testing on pharmaceutical products according to client/compendia procedures and departmental SOPs.

You will be part of a fast-paced environment where agility, adaptability, and high standards go hand in hand. The role requires disciplined, science-based approaches that ensure consistent excellence, safety, and integrity in everything you do.

GRAM offers the opportunity to grow within a company that values community involvement, starting day 1 benefits, and generous paid time off. Full job description is available during the formal interview process.

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
Proficient computer skills in Microsoft Word, Excel, and Outlook
Ability to learn new techniques, perform multiple tasks simultaneously, and keep accurate records
Excellent written and verbal skills to communicate effectively with management, staff, and regulatory agencies

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 starting day 1
401(k) program with immediate vesting of contributions and employer contributions
Generous off-shift premiums
16 hours of paid volunteer time per calendar year
Paid time off: up to 104 hours per year, prorated first year, plus wellness time off (1 hour per 30 hours worked)
10 paid holidays per year with immediate eligibility