JLL
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. Your day-to-day tasks will include:
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 This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without employer sponsorship. Location
On-site – Houston, TX If this job description resonates with you, we encourage you to apply, even if you don’t meet all the requirements. We’re interested in getting to know you and what you bring to the table! Personalized benefits that support personal well-being and growth
JLL recognizes the impact that the workplace can have on your wellness, so we offer a supportive culture and comprehensive benefits package that prioritizes mental, physical and emotional health. Some of these benefits may include: 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 Jones Lang LaSalle (JLL) is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process – including the online application and/or overall selection process – you may email us at HRSCLeaves@jll.com. This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page. I want to work for JLL. Accepting applications on an ongoing basis until candidate identified.
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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 will include:
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 This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without employer sponsorship. Location
On-site – Houston, TX If this job description resonates with you, we encourage you to apply, even if you don’t meet all the requirements. We’re interested in getting to know you and what you bring to the table! Personalized benefits that support personal well-being and growth
JLL recognizes the impact that the workplace can have on your wellness, so we offer a supportive culture and comprehensive benefits package that prioritizes mental, physical and emotional health. Some of these benefits may include: 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 Jones Lang LaSalle (JLL) is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process – including the online application and/or overall selection process – you may email us at HRSCLeaves@jll.com. This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page. I want to work for JLL. Accepting applications on an ongoing basis until candidate identified.
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