QA Inspector- Pharmaceutical

As a Quality Assurance Inspector in Southeastern Massachusetts, you will play a vital role in ensuring the quality and compliance of pharmaceutical manufacturing operations. With a minimum of 3 years of hands-on QA experience in a regulated cGMP pharmaceutical production setting, your primary responsibility will be to conduct on-the-floor quality inspections and monitor manufacturing processes. Your keen attention to detail and understanding of cGMP standards will be instrumental in maintaining regulatory and internal quality standards. Your day-to-day tasks will include conducting routine in-process checks, performing line clearance and area readiness checks, executing visual inspections, and submitting product samples for laboratory analysis. You will also be responsible for maintaining and calibrating standard weights, tracking facility conditions, reviewing support documentation, and confirming equipment functionality during manufacturing runs. Additionally, you will assist in investigations of quality-related complaints, document any non-conformities, and participate in cross-functional improvement projects. To qualify for this role, you must have a high school diploma or equivalent, with additional training or coursework in pharmaceutical manufacturing or life sciences preferred. Direct experience with MDI manufacturing is advantageous but not mandatory. A solid understanding of GMP regulations, proficiency in using tools like Microsoft Word and Excel, excellent communication skills, and the ability to work both independently and collaboratively in a fast-paced production setting are essential for success in this position. If you have a minimum of 10 years of experience as a Quality Assurance Inspector in the pharmaceutical industry, with expertise in GMP, CGMP, manufacturing, MDI, solid dosage forms, liquids, tablets, and capsules, and you are looking for a full-time role where you can contribute to maintaining high-quality standards in pharmaceutical production, we encourage you to apply for this opportunity. This position requires in-person work and an expected commitment of 40 hours per week.,