JLL
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Quality Specialist
role at
JLL .
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.
Your day‑to‑day tasks
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
Required Qualifications
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
Preferred Qualifications
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
Seniority Level
Associate
Employment type
Full‑time
Job function
Quality Assurance
Referrals increase your chances of interviewing at JLL by 2x
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Quality Specialist
role at
JLL .
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.
Your day‑to‑day tasks
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
Required Qualifications
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
Preferred Qualifications
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
Seniority Level
Associate
Employment type
Full‑time
Job function
Quality Assurance
Referrals increase your chances of interviewing at JLL by 2x
#J-18808-Ljbffr