QC Chemist I

1w1 week ago

Grand River Aseptic Manufacturing

Grand Rapids, US · Full-time

About this role

The QC Chemist I supports quality systems as they relate to the manufacturing and testing of cGMP drug products at Grand River Aseptic Manufacturing. This role provides general laboratory support focused on raw materials and excipient testing used in finished products. The position suits candidates who value agility, impact, and a disciplined, science-based methodology.

Daily work centers on performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients, excipients, and finished pharmaceutical products. Analysts prepare standards and samples, then operate instrumentation such as HPLC, FTIR, UV VIS, and physical testing equipment according to client and compendia procedures.

Team members review laboratory data for accuracy and regulatory adherence while processing results and generating reports. All activities occur in a fast-paced environment that demands precise record-keeping and strict compliance with cGMPs, company SOPs, and current industry practice.

GRAM offers immediate access to medical, dental, vision, life, and disability coverage with company cost sharing. Employees also receive 401(k) immediate vesting, paid volunteer time, PTO, wellness time off, and ten paid holidays from day one.

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; 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 on first day with company paying a portion of the cost.
401(k) program with all contributions immediately 100% vested.
Generous off-shift premiums.
16 hours of paid volunteer time per calendar year starting day one.
PTO accrual up to 104 hours per year, prorated first year.
Wellness time off earned at 1 hour per 30 hours worked.
10 paid holidays per calendar year with immediate eligibility.