Quality Operations Manager
$125k - $155kAstrix Technology
Quality Operations Manager
Manufacturing
Ridgefield, New Jersey, US
- Added - 20/04/2026
Pay Rate Low: 125000 | Pay Rate High: 155000
Our client, a personal care manufacturer, is seeking a Plant Quality Manager to provide both strategic direction and hands-on leadership across all quality functions within a high-volume, FDA-regulated OTC manufacturing facility.
Title: Plant Quality Manager - OTC Manufacturing
Salary: $125,000 - $155,000 + annual bonus
Location: Ridgefield, NJ (Fully Onsite) Excellent relocation package!
Relocation Assistance: Available
Schedule: Monday-Friday 7:30am (start time)
Direct Hire
About the Role
This role is responsible for ensuring GMP compliance, strengthening the site's quality systems, and fostering a strong culture of quality and operational excellence.
This is a highly visible leadership position requiring a hands-on professional who can work directly on the production floor, rebuild and develop teams, and drive continuous improvement initiatives in a fast-paced manufacturing environment.
Key Responsibilities
Lead Quality Assurance, Quality Control Labs, Document Control, Validation, and Complaint Management teams
Oversee and enhance the site's Quality Management System (QMS) in alignment with FDA and corporate standards
Serve as the site quality leader during FDA and customer inspections; ensure continuous inspection readiness
Drive resolution of compliance issues and manage CAPAs effectively
Collaborate cross-functionally with Operations, Engineering, and R&D on investigations, change control, and validation activities
Oversee batch record review, product release, deviations, and investigations
Partner with customers and internal stakeholders to meet quality and compliance expectations
Analyze quality metrics and implement improvements to drive performance
Coach, mentor, and develop a high-performing quality team
Represent site quality leadership in executive-level discussions
Contribute to broader quality strategy and site expansion initiatives
Qualifications
Education
Bachelor's degree in Chemistry, Microbiology, Pharmacy, Chemical Engineering, or a related field
Masters degree is a plus
Experience
10+ years in FDA-regulated environments (OTC, pharmaceutical, or personal care manufacturing)
10+ years leading FDA inspections and remediation efforts
Experience with topical formulations strongly preferred
Proven leadership experience in a manufacturing environment
INDBH
#LI-MG1
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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