Life Sciences Quality & Compliance Leader

JLL; Gurabo (PR); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

401(k) plan with matching company

Comprehensive Medical, Dental & Vision

Paid parental leave at 100% of salary

Paid Time Off and Company Holidays

Daily Pay

Job summary

JLL is seeking a seasoned Quality & Compliance leader to drive regional programs across assigned sites, ensuring FDA-regulated manufacturing compliance and audit readiness. You will develop CAPAs, lead investigations, and maintain documentation robustly.

You will collaborate with client quality units, mentor staff, and ensure continuous improvement in quality metrics and contractual scoring. This role demands strong communication and a detail-oriented approach.

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/compliance

FDA regulations

cGMPs knowledge

Quality Management Systems

Documentation management

MS Office (Excel/Word/PowerPoint)

Communication

Leadership/mentoring

Education

Bachelor's degree (related field)

6+ years pharma quality/compliance experience

EIT/PE certification (preferred)

Tools

TrackWise

SuccessFactors

Infinity

Veeva

Job description

JLL is seeking a seasoned Quality & Compliance leader to drive regional programs across assigned sites, ensuring FDA-regulated manufacturing compliance and audit readiness. You will develop CAPAs, lead investigations, and maintain documentation robustly.

You will collaborate with client quality units, mentor staff, and ensure continuous improvement in quality metrics and contractual scoring. This role demands strong communication and a detail-oriented approach.