Quality Specialist

This job is with JLL, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

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

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For more information about how JLL processes your personal data, please view our Candidate Privacy Statement.

For additional details please see our career site pages for each country.

For candidates in the United States, please see a full copy of our Equal Employment Opportunity policy here.

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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