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Quality and Compliance Manager

United States, Summit, NJ 95000.00 - 115000.00 USD / Year · Job Posted February 20, 2026
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Job Description

The Quality & Compliance Manager oversees quality assurance operations for JLL's facilities team and subcontractors within a cGMP bio-pharmaceutical manufacturing environment. This role ensures full compliance with contractual, procedural, and regulatory requirements while maintaining oversight of maintenance, repairs, and facility operations. The position requires deep knowledge of FDA regulations and cGMPs, with responsibility for developing and managing quality management systems, SOPs, investigations, CAPAs, audits, and training materials. The manager serves as the primary interface with the client's quality organization, ensuring all work performed by JLL teams meets strict documentation and compliance standards. This role is instrumental in fostering a quality-first culture across a highly matrixed organizational structure while managing GxP contractor compliance programs and supporting continuous improvement initiatives.

Job Responsibility

  • Oversee regulatory and quality compliance activities across all facilities team operations and subcontractors
  • Prepare, review, and manage SOPs, quality investigations, deviations, CAPAs, and change control documentation
  • Interface with client quality organization to ensure adherence to all quality procedures and proper work documentation
  • Manage GxP contractor compliance programs including qualification, agreements, audits, and performance monitoring
  • Conduct quality audits and assessments of building systems such as HVAC, critical environments, and utilities
  • Collaborate with maintenance teams to support quality investigations and root cause analysis
  • Provide quality guidance and training to facilities staff, vendors, and service providers
  • Monitor and report on Key Performance Indicators and Service Level Agreement compliance
  • Review and approve technical documentation and quality reports for client delivery
  • Support continuous improvement initiatives and quality system enhancements

Requirements

  • Bachelor's degree in Science or Engineering
  • Minimum 3 years of experience in quality engineering, facilities operations, or production operations in a cGMP environment
  • Prior experience working in an FDA-regulated bio-pharmaceutical manufacturing facility
  • Knowledge of FDA regulations 21 CFR Parts 210, 211, or Part 820
  • Understanding of current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP)
  • Experience with quality management systems including investigations, CAPAs, audit programs, and vendor qualification
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Candidates must be authorized to work in the United States without sponsorship

Nice to have

  • Engineering background or equivalent technical experience
  • Working knowledge of electronic Quality Management Systems (TrackWise, Success Factors, Veeva, MasterControl)
  • Experience with GxP building systems oversight (HVAC, critical environments, utilities)
  • Experience managing contractor and vendor compliance programs
  • Background in facilities maintenance and repair within pharmaceutical manufacturing
  • Willingness to travel approximately 10%
  • Experience writing detailed technical reports and quality documentation

What we offer

  • 401(k) plan with matching company contributions
  • Comprehensive Medical, Dental & Vision Care
  • Paid parental leave at 100% of salary
  • Paid Time Off and Company Holidays
  • Early access to earned wages through Daily Pay

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