Quality Specialist

Quality Specialist – JLL

The Quality Specialist provides comprehensive quality assurance support for facility maintenance operations in a regulated pharmaceutical environment. The role ensures that JLL and client procedures, FDA regulations, and applicable global quality standards are consistently met.

• Quality Compliance & Regulatory Support: Execute cGMP quality compliance programs for facilities maintenance activities and ensure all maintenance operations comply with FDA, EU, and other applicable regulatory expectations.
• Audit Readiness & Self-Assessments: Conduct routine self‑inspections and facility walk‑throughs to maintain continuous readiness; identify quality risks and partner with operations to implement corrective and preventive actions.
• Training & Personnel
  
  Qualification:
  
  Develop and update training materials for facilities maintenance personnel; maintain personnel qualification and training records; train, mentor, and coach JLL staff on cGMP expectations, quality systems, and SOP adherence.
• Quality Event Tracking & CAPA Support: Track quality events, deviations, and observations to ensure timely follow‑up and closure; partner with operations leadership to drive root‑cause analysis and corrective actions.
• Stakeholder & Client
  
  Collaboration:
  
  Serve as the key interface with client Quality Assurance personnel; ensure alignment on documentation practices, SOP updates, and regulatory procedures; support achievement of quality KPIs defined in the Service Level Agreement.
• Documentation & Systems: Maintain high‑quality documentation consistent with ALCOA+ data integrity principles; utilize and support documentation control systems, maintenance systems, and quality‑related software tools; support change management processes and ensure governance around controlled documents.

• Bachelor’s degree in a scientific, engineering, or technical field.
• Minimum 3 years of experience in pharmaceutical, biotech, medical device, or life sciences environments operating under GMP regulations.
• 1–2 years of experience in quality assurance, regulatory compliance, deviation management, or audit support.
• Strong computer proficiency in Word, Excel, and PowerPoint.
• Excellent written and verbal communication skills.
• Strong analytical abilities – able to diagnose issues, evaluate options, and drive effective resolutions.

• Auditing experience in pharmaceutical or regulated manufacturing environments.
• Experience with documentation control systems, building control/maintenance systems, and change‑control processes.
• Background in facilities maintenance operations in GMP settings.
• Knowledge of Quality Management Systems and continuous improvement methodologies.
• Experience developing training content for technical teams.
• Familiarity with customer satisfaction survey processes and quality KPI management.
• Professional certifications such as ASQ, RAC, IFM, or cGMP‑related credentials.

Onsite – New Albany, Ohio. Shift: Monday to Friday, 2nd shift (12pm to 8pm or 3pm to 11pm).

$67,000 to $97,000 plus 7.5% bonus.

• 401(k) plan with matching company contributions.
• Comprehensive medical, dental, and vision care.
• Paid parental leave at 100% of salary.
• Paid time off and company holidays.
• Early access to earned wages through Daily Pay.

JLL is an Equal Opportunity Employer committed to diversity and inclusion. This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without sponsorship.