QA Supervisor, GMP Manufacturing - Lead & Improve

Nitto Avecia; Milford (MA); On-site; USD 75,000 - 94,000; Full time

Job summary

Nitto Avecia is seeking an experienced Manufacturing Quality Assurance Supervisor to oversee the MQA team across three shifts and ensure day-to-day quality oversight for manufacturing activities. You will drive cGMP compliance, mentor QA staff, and lead continuous improvement initiatives in collaboration with Manufacturing.

The role requires strong regulatory knowledge (GxP), people leadership, and the ability to manage deviations and CAPAs while maintaining effective cross-functional

Qualifications

• 8+ years in a regulated/GMP industry; QA Pharma/Biotech experience preferred.
• 2+ years people management experience.
• Strong knowledge of ICH/ISO/cGMP/ USP/EU guidelines and CFR 21 parts 210/211; ICH Q7/9/10 is desirable.
• Able to work in fast-paced environment with cross-functional teams.

Responsibilities

• Oversee 3 shifts and lead the MQA team with guidance and organization.
• Create, maintain, and report on KPIs for the MQA team.
• Review and update SOPs and deviations/CAPAs.
• Train, mentor, and lead quality teams for routine MQA activities and improvements.
• Collaborate with Manufacturing to ensure cGMP adherence and communicate with MFG leadership.
• Lead meetings between MFG and QA; on-the-floor monitoring and logbook/batch record review.

Skills

GxP knowledge

Leadership

QA in pharma/biotech

Problem solving

Job description

Nitto Avecia is seeking an experienced Manufacturing Quality Assurance Supervisor to oversee the MQA team across three shifts and ensure day-to-day quality oversight for manufacturing activities. You will drive cGMP compliance, mentor QA staff, and lead continuous improvement initiatives in collaboration with Manufacturing.

The role requires strong regulatory knowledge (GxP), people leadership, and the ability to manage deviations and CAPAs while maintaining effective cross-functional