Quality Specialist

JLL-posted 2 days ago

Full-time • Mid Level

Onsite • Houston, TX

5,001-10,000 employees

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JLL empowers you to shape a brighter way . Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you’ve got deep experience in commercial real estate, skilled trades or technology, or you’re looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. What this job involves This position provides comprehensive quality assurance support for pharmaceutical facility operations, ensuring all maintenance activities comply with company policies, client procedures, and FDA cGMP regulations. The Quality Specialist maintains the highest quality standards in regulated manufacturing environments while supporting continuous improvement initiatives and working closely with facility management teams and client quality control personnel.

Executing Quality Compliance programs for cGMP manufacturing facilities and ensuring full regulatory adherence
Conducting facility self-assessments and vendor/supplier audits to maintain quality standards
Preparing and revising SOPs, change control documentation, investigations, and CAPAs
Developing training materials for facilities maintenance teams and maintaining personnel qualification files
Tracking and following up on quality events with department managers to ensure resolution
Supporting achievement of Key Performance Indicators outlined in Service Level Agreements
Interfacing with client quality control personnel to ensure proper documentation and SOP adherence

Bachelor's degree in Engineering or equivalent experience in related field
Minimum 5 years of experience in pharmaceutical, biotech, or life sciences sectors under GMP regulations
Minimum 4 years of regulatory quality and statutory compliance experience
Quality Assurance role experience in FDA-regulated manufacturing facilities
Strong knowledge of cGMP regulations as applied to maintenance and manufacturing equipment
Proficiency with Quality Engineering techniques, CMMS systems, and Quality Management Systems
Advanced computer skills including Microsoft Word, Excel, and PowerPoint
This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without employer sponsorship.

Auditing experience in pharmaceutical or regulated manufacturing environments
Experience with documentation control systems and change management processes
Background in facility maintenance operations within pharmaceutical settings
Knowledge of Quality Management Systems implementation and continuous improvement methodologies
Experience developing training programs for technical teams
Familiarity with client satisfaction survey processes and KPI management
Self-motivated and detail-oriented work style with ability to function independently in dynamic team environments

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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