Quality Supervisor
Perrigo Company plc
September 02, 2026
On-site
Bronx, NY
Operations
Scope of the Role:
The QA Supervisor leads a team of Quality Assurance Inspectors providing quality oversight for bulk manufacturing, filling, and packaging for topical and suppository pharmaceutical products. Ensures compliance with cGMP, FDA regulations, internal quality systems, and approved procedures.
Responsibilities:
- Supervise, coach, train, and evaluate QA Inspectors for in-process oversight.
- Ensure manufacturing and packaging comply with cGMP, FDA requirements, approved procedures, batch records, and internal standards.
- Review production, packaging, and quality documentation for accuracy, completeness, and compliance.
- Provide real-time quality support, address quality concerns, conduct risk assessments, and escalate issues.
- Author/revise/review/approve SOPs, SWIs, forms, and other controlled documents; develop/improve procedures and quality systems.
- Lead/support investigations for deviations, non-conformances, documentation errors, environmental monitoring excursions, and other quality events; ensure CAPA implementation.
- Monitor compliance trends and identify continuous improvement opportunities.
- Schedule/prioritize team activities; ensure GMP qualifications and training are maintained.
- Support FDA inspections, customer audits, and internal audits; maintain inspection readiness and assist with remediation.
- Support quality metrics, management reviews, and other quality system initiatives.
Experience Required:
- Bachelor’s degree in a scientific discipline preferred; equivalent regulated experience may substitute.
- 4+ years Quality Assurance experience in a regulated industry.
- Prior pharmaceutical/biotech/medical device/cosmetics or other FDA-regulated manufacturing experience required.
- Knowledge of cGMP and quality systems.
- Experience reviewing documentation/investigations, deviations, CAPAs, and change controls.
- Experience authoring/revising SOPs and controlled documents.
- Supervisory/leadership experience preferred.
- FDA inspections/audits support experience preferred.
- Strong written, verbal, organizational, and interpersonal skills.
- SAP and/or electronic quality management system (eQMS) knowledge preferred.
Schedule:
- First shift, Monday–Friday; occasional weekend on-call support.
Salary:
- $80,000.
Benefits:
- Competitive compensation, benefits for you and your family, and career development opportunities.
Application Instructions:
- Click the APPLY button at the bottom of the application. Submit resumes/CVs in English.
The QA Supervisor leads a team of Quality Assurance Inspectors providing quality oversight for bulk manufacturing, filling, and packaging for topical and suppository pharmaceutical products. Ensures compliance with cGMP, FDA regulations, internal quality systems, and approved procedures.
Responsibilities:
- Supervise, coach, train, and evaluate QA Inspectors for in-process oversight.
- Ensure manufacturing and packaging comply with cGMP, FDA requirements, approved procedures, batch records, and internal standards.
- Review production, packaging, and quality documentation for accuracy, completeness, and compliance.
- Provide real-time quality support, address quality concerns, conduct risk assessments, and escalate issues.
- Author/revise/review/approve SOPs, SWIs, forms, and other controlled documents; develop/improve procedures and quality systems.
- Lead/support investigations for deviations, non-conformances, documentation errors, environmental monitoring excursions, and other quality events; ensure CAPA implementation.
- Monitor compliance trends and identify continuous improvement opportunities.
- Schedule/prioritize team activities; ensure GMP qualifications and training are maintained.
- Support FDA inspections, customer audits, and internal audits; maintain inspection readiness and assist with remediation.
- Support quality metrics, management reviews, and other quality system initiatives.
Experience Required:
- Bachelor’s degree in a scientific discipline preferred; equivalent regulated experience may substitute.
- 4+ years Quality Assurance experience in a regulated industry.
- Prior pharmaceutical/biotech/medical device/cosmetics or other FDA-regulated manufacturing experience required.
- Knowledge of cGMP and quality systems.
- Experience reviewing documentation/investigations, deviations, CAPAs, and change controls.
- Experience authoring/revising SOPs and controlled documents.
- Supervisory/leadership experience preferred.
- FDA inspections/audits support experience preferred.
- Strong written, verbal, organizational, and interpersonal skills.
- SAP and/or electronic quality management system (eQMS) knowledge preferred.
Schedule:
- First shift, Monday–Friday; occasional weekend on-call support.
Salary:
- $80,000.
Benefits:
- Competitive compensation, benefits for you and your family, and career development opportunities.
Application Instructions:
- Click the APPLY button at the bottom of the application. Submit resumes/CVs in English.