QC Chemist – GMP Analytical Testing for Drug-Device

Abbott (abbottcareers2 board); United States; On-site; USD 70,000 - 100,000; Full time

Job summary

Abbott in Minnetonka, MN, seeks a Quality Control Chemist to support analytical testing for commercial products in a GMP-regulated laboratory. The role involves batch release, stability, raw material, and investigational testing using HPLC, GC, FTIR, UV-Vis, and other techniques.

The successful candidate will generate high-quality data, maintain compliant documentation, and ensure adherence to GMP, USP/EP guidance, and internal procedures while collaborating across QA, Manufacturing, Regulatory,

Qualifications

• Bachelor's degree in chemistry or closely related field.
• 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 Certificates of Analysis, testing summaries, and technical reports.
• Maintain accurate laboratory records in compliance with GMP and data integrity standards.
• Collaborate with QA, Manufacturing, Regulatory Affairs, and R&D teams.

Skills

HPLC/UPLC analysis

GMP compliance

Analytical testing

Education

Bachelor's degree in Chemistry / Analytical Chemistry / Pharmaceutical Sciences

Tools

HPLC

UPLC

GC

Dissolution

FTIR

UV-Vis

Karl Fischer titration

pH meters

Analytical balances

Job description

Abbott in Minnetonka, MN, seeks a Quality Control Chemist to support analytical testing for commercial products in a GMP-regulated laboratory. The role involves batch release, stability, raw material, and investigational testing using HPLC, GC, FTIR, UV-Vis, and other techniques.

The successful candidate will generate high-quality data, maintain compliant documentation, and ensure adherence to GMP, USP/EP guidance, and internal procedures while collaborating across QA, Manufacturing, Regulatory,