The Analytical QA Supervisor role in Fall River MA requires 8-15 years of pharmaceutical QA experience, including 5+ years in analytical roles within cGMP labs.
Responsibilities include overseeing method validations, ensuring cGLP compliance, reviewing SOPs, lab data, and process validation reports, and supporting regulatory submissions.
Candidates should have a chemistry or related degree, strong knowledge of analytical instruments (HPLC, GC, UV), and familiarity with FDA, USP, and ICH standards.
This full-time, on-site position involves laboratory oversight, audits, documentation management, and cross-functional projects, with occasional weekend or holiday shifts.
Relocation assistance is negotiable, and adherence to GMP standards is mandatory.
Must have pharma industry experience, scientific background, QA expertise, and excellent communication skills in English.