CareerPlan

Quality Control Analyst III

Massachusetts, USFull-time$90k–$110k2026-10-30 → 2026-11-10
On-site

Core

Perform chemical and physical analyses of raw materials, in-process materials, and drug products to support product development, release, and stability testing in a cGMP environment.

Role type

Quality Control Analyst (Analytical Chemistry)

Builds

Drug products (inhalation therapies) via analytical testing and data reporting

Domain

Life Sciences / Pharmaceutical Manufacturing (cGMP)

Required skills

HPLC, UPLC, GC, UV-vis, FTIR, laser diffraction, KF, Empower software, statistical data analysis, SOP revision, laboratory investigations

Preferred skills

MDI/DPI analytical test methods (Andersen Cascade Impactor, Emitted Dose), analytical method development and validation

Technologies

HPLC, UPLC, GC, UV-vis, FTIR, laser diffraction, KF, Empower, Microsoft Office

Responsibilities

Operate analytical instrumentation; analyze data for trending and regulatory filings; monitor equipment calibration; participate in quality investigations; revise SOPs and test procedures; identify and implement corrective actions

Seniority

Mid-level (4-6 years experience)