QC Chemist I

4w1 month ago

Grand River Aseptic Manufacturing

Grand Rapids, US · Full-time · $50,000 – $65,000

About this role

The QC Chemist I supports quality systems related to the manufacturing and testing of cGMP drug products. This includes providing general laboratory support for raw materials and excipient testing used in finished products, essential for ensuring consistent excellence and safety.

Daily responsibilities involve performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products. The chemist independently runs HPLC, FTIR, UV-Vis, and physical testing while preparing standards and samples.

GRAM fosters a fast-paced environment where agility, adaptability, and high standards go hand in hand, driven by a disciplined, science-based approach that promotes integrity and community. The team is dedicated to making a meaningful impact through their work and support of others, encouraging collaboration and commitment to excellence.

GRAM offers benefits starting on day one, including medical and 401(k) with immediate vesting, as well as paid volunteerism and generous time off. These perks support personal well-being and community involvement, providing opportunities for professional growth within the aseptic manufacturing industry.

Requirements

Bachelor's degree in Chemistry or related discipline (e.g., Biochemistry, Biotechnology).
Minimum of 1-3 years pharmaceutical or testing experience.
Qualification for use of a full-face respirator.
Proficient computer skills in Microsoft Word, Excel, and Outlook.
Excellent written and verbal communication 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 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.
Provide general laboratory support for raw materials and excipient testing used in finished product.

Benefits

Medical, prescription, dental, vision, life insurance, and disability benefits available starting day 1.
401(k) program with immediate 100% vesting of contributions.
16 hours of paid volunteer time per calendar year.
Full-time employees accrue up to 104 hours of paid time off per calendar year (prorated first year).
Wellness time off: 1 hour for every 30 hours worked.
10 paid holidays per calendar year with immediate eligibility.
Generous off-shift premiums.