QA Supervisor: Pharma Manufacturing & Compliance Lead

Perrigo Company plc; New York (NY); On-site; USD 72,000 - 88,000; Full time

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Job summary

Perrigo Company plc in New York is seeking a QA Supervisor to lead a team of QA Inspectors responsible for in-process oversight of manufacturing and packaging of topical and related products. You will ensure compliance with cGMP, FDA regulations, and internal quality systems.

You will review documentation, support investigations and audits, develop and approve SOPs, lead corrective actions, and drive continuous improvement while coordinating training and GMP qualifications for the team.

Qualifications

• Bachelor's degree in a scientific discipline preferred; equivalent regulated experience may be considered.
• Minimum of four years of Quality Assurance experience in a regulated industry.
• Experience in pharmaceutical/biotech/medical device or other FDA-regulated environments.
• Demonstrated knowledge of cGMP requirements and quality systems.
• Experience reviewing manufacturing and packaging documentation, investigations, deviations, CAPAs, and change controls.
• Experience authoring and revising SOPs and other controlled documents.
• Previous supervisory or leadership experience preferred.
• Experience supporting FDA inspections and audits preferred.
• Strong written, verbal, organizational, and interpersonal skills.
• Knowledge of SAP and/or electronic quality management systems (eQMS) preferred.

Responsibilities

• Supervise, coach, train, and evaluate QA Inspectors responsible for in-process oversight of manufacturing and packaging operations.
• Ensure manufacturing and packaging activities comply with cGMP, FDA regulations, approved procedures, batch records, and internal quality standards.
• Review production, packaging, and quality documentation for accuracy, completeness, and compliance.
• Provide quality support to operations by addressing quality concerns, conducting risk assessments, and escalating issues when appropriate.
• Author, revise, review, and approve SOPs, Standard Work Instructions (SWIs), forms, and other controlled documents; develop new procedures and improve existing quality systems as needed.
• Lead or support investigations involving deviations, non-conformances, documentation errors, environmental monitoring excursions, and other quality events, ensuring timely implementation of corrective and preventive actions.
• Monitor compliance trends and identify opportunities for continuous improvement.
• Schedule and prioritize team activities and ensure personnel maintain required GMP qualifications and training.
• Support FDA inspections, customer audits, and internal audits while maintaining inspection readiness and assisting with remediation activities.
• Assist with quality metrics, management reviews, and other quality system initiatives.

Skills

Quality Assurance

cGMP Knowledge

Investigations

CAPA

SOPs

Leadership

Audits

Education

Bachelor's degree (scientific)

Tools

SAP

eQMS

Job description

Perrigo Company plc in New York is seeking a QA Supervisor to lead a team of QA Inspectors responsible for in-process oversight of manufacturing and packaging of topical and related products. You will ensure compliance with cGMP, FDA regulations, and internal quality systems.

You will review documentation, support investigations and audits, develop and approve SOPs, lead corrective actions, and drive continuous improvement while coordinating training and GMP qualifications for the team.