Senior Quality & Compliance Lead — Life Sciences

Jones Lang LaSalle Incorporated; Gurabo (PR); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

401(k) plan with matching company

Medical, Dental & Vision

Paid parental leave

Paid Time Off and Holidays

Daily Pay access

Job summary

Jones Lang LaSalle (JLL) in Gurabo, PR seeks a senior quality and compliance professional to lead quality programs across pharmaceutical/biotech facilities. You will develop CAPAs, manage non-conformances, and drive vendor qualification to ensure regulatory alignment.

The role requires deep knowledge of cGMPs and FDA regulations (21 CFR 11, 210, 211, 600, 820) and ISO 9001:2015, with strong communication and mentoring skills to guide site staff toward continuous improvement.

Qualifications

• Bachelor's degree with minimum 6 years of experience in quality/compliance programs for pharmaceutical/biotechnology/medical devices facilities
• Thorough understanding of cGMPs as they relate to facilities, utilities, equipment, and laboratories supporting pharmaceutical manufacturing
• Strong knowledge of FDA guidance documents and regulations including 21CFR parts 11, 210, 211, 600, and 820
• Proven expertise in Quality Management Systems including Investigations/RCA, CAPAs, Audit programs, and Document Management
• Excellent PC skills with proficiency in MS Office applications, particularly Excel, Word, and PowerPoint
• Excellent oral and written communication skills for interfacing with all management levels and diverse customer base
• Demonstrated ability to work independently while effectively leading and mentoring team members

Responsibilities

• Develop, implement, and support quality programs including Non-Conformance Investigations, CAPAs, Training Compliance, and Vendor Qualifications
• Build and maintain successful relationships with account personnel and client stakeholders to promote confidence and best practices
• Interface with client quality personnel to ensure all requirements are followed and work is properly documented and recorded
• Perform and support audits while preparing documents and training materials for site staff performance enhancement
• Manage and report on Quality and Compliance critical performance measurements and develop status reports for Quality Programs
• Lead staff through clear communication of expectations, accountability, and continuous improvement performance feedback
• Ensure JLL's Life Sciences Quality Management System implementation including ISO 9001:2015 requirements compliance

Skills

Quality leadership

cGMP knowledge

FDA guidance knowledge

Quality Management Systems

MS Office proficiency

Communication skills

Mentoring & leadership

Education

Bachelor's degree + 6 years exp

Tools

TrackWise

SuccessFactors

Infinity

Veeva

Job description

Jones Lang LaSalle (JLL) in Gurabo, PR seeks a senior quality and compliance professional to lead quality programs across pharmaceutical/biotech facilities. You will develop CAPAs, manage non-conformances, and drive vendor qualification to ensure regulatory alignment.

The role requires deep knowledge of cGMPs and FDA regulations (21 CFR 11, 210, 211, 600, 820) and ISO 9001:2015, with strong communication and mentoring skills to guide site staff toward continuous improvement.