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6 Astrix Jobs Hiring in Ridgefield, NJ

Astrix Inc

Quality Operations Manager

Ridgefield, NJ · On-site

$125K - $155K/yr

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 ...

Astrix Inc

Database Specialist

Fairfield, NJ · On-site

$50 - $70/hr

Our client is an Environmental Laboratory are seeking a highly technical LIMS Database Specialist . This individual will play a critical role in maintaining, optimizing, and enhancing the Laboratory ...

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Quality Operations Manager

Quality Operations Manager

Astrix Inc

Ridgefield, NJ • On-site

$125K - $155K/yr

Full-time

Posted 27 days ago

Job description

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

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