Quality Control Chemist - GMP Lab & HPLC Expert

Abbott

United States

On-site

USD 65,000 - 90,000

Full time

2 days ago

Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Abbott in Minnetonka, MN is seeking a Quality Control Chemist to perform analytical testing in a GMP-regulated QC lab supporting commercial products and stability programs. You will generate high-quality data, maintain proper documentation, and ensure compliance with GMP, USP/EP, and internal procedures.

The role involves hands-on HPLC/UPLC analysis, dissolution, GC, FTIR, UV-Vis, Karl Fischer, and other instrumentation, with collaboration across QA, Manufacturing, Regulatory Affairs, and R&D

Qualifications

Bachelor's degree in chemistry, analytical chemistry, pharmaceutical sciences, or related scientific discipline.
Minimum of 2 years of experience in a GMP-regulated analytical laboratory.
Hands-on experience performing HPLC/UPLC analyses.

Responsibilities

Perform analytical testing to support batch release and stability programs for combination drug-device products.
Evaluate analytical results against product specifications and acceptance criteria.
Generate testing summaries, Certificates of Analysis (CoA), and technical reports as required.
Maintain accurate, complete, and contemporaneous laboratory records in compliance with GMP and data integrity requirements.
Collaborate with QA, Manufacturing, Regulatory Affairs, and R&D teams.

Skills

GMP-regulated lab experience

HPLC/UPLC experience

Education

Bachelor's degree in Chemistry or related

Tools

HPLC/UPLC instruments

Job description

The role involves hands-on HPLC/UPLC analysis, dissolution, GC, FTIR, UV-Vis, Karl Fischer, and other instrumentation, with collaboration across QA, Manufacturing, Regulatory Affairs, and R&D

Get your free, confidential resume review.

or drag and drop your file here.