Top 31 Quality manager Jobs in Willis, Tx

Associate Director - QA
Bionova Scientific LLC —The Woodlands, TX
- $150,000 - $164,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Bachelor's degree
2d
Nuclear Supplier Quality Manager
System One —The Woodlands, TX
- $100,000 - $150,000 a year
- Hybrid work
- 7 years
- Computer literacy
- Engineering
- Health insurance
- Dental insurance
Quick Apply
6d
Quality Manager
Full Circle Recruiting —Conroe, TX
- Full-time
- Management
- 8 years
- Analysis skills
Quick Apply
14d
Quality Manager - Stabil Drill
Stabil Drill —Conroe, TX
- Basic math
- Computer skills
- Senior level
- Disability insurance
- Health insurance
5h
QHSE Manager
DCL America Inc. —Oak Ridge North, TX
- $80,000 - $100,000 a year
- Full-time
- 5 years
- Engineering
- Supervising experience
Quick Apply
Quality Manager
NAES Corporation —Spring, TX
- $123,500 - $142,050 a year
- Extended hours
- Remote
- Oracle
- Engineering
- Pass drug screening
Quick Apply
Quality Manager
Panelmatic —Conroe, TX
- Full-time
- Background check
- Management
- Ability to walk for extended periods
- Health savings account
- AD&D insurance
Quick Apply
Quality Assurance Manager - Eurofins Drinking Water and Wastewater Central - Huntsville, TX
Eurofins USA Environment Testing —Huntsville, TX
- $60,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- English
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
17h
QA/QC Manager
AG&P Americas Inc. —Spring, TX
- Full-time
- Construction site
- Ability to walk for extended periods
- Engineering
Quick Apply
FCW-SH99 JV Deputy Construction Quality Control Manager
Ferrovial Construction —The Woodlands, TX
- Full-time
- Microsoft Excel
- Construction site
- 5 years
13d
FCW-SH99 JV - Quality Control Manager
Ferrovial Construction —The Woodlands, TX
- Full-time
- Civil engineering
- Management
- Construction site
Associate Director - QA
Asahi Kasei —The Woodlands, TX
- $150,000 - $164,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Bachelor's degree
2d
QA Lead, Quality Systems (Cell Therapy)(W)
Cellipont Bioservices —The Woodlands, TX
- Full-time
- Bachelor of Science
- Bachelor's degree
- Mentoring
- Paid holidays
- Tuition reimbursement
Quick Apply
Nuclear Supplier Quality Manager
Chart, Inc. —The Woodlands, TX
- Computer literacy
- Engineering
- ERP systems
Quick Apply
Senior Water Quality Environmental Consultant (Project Manager) - TX
CK Associates —The Woodlands, TX
- Full-time
- Clean driving record
- 8 years
- Travel
Quick Apply
Janitorial Quality Assurance / Field Supervisor - Conroe & The Woodlands, TX
iClean Maids —Houston, TX
- $50 a day
- Part-time
- Reliable transportation
- Senior level
- Commercial
- Paid training
- Opportunities for advancement
Quick Apply
1d
Janitorial Quality Assurance / Field Supervisor - Graveyard Shift (Part-time)
iClean Maids —Houston, TX
- $50 a day
- Part-time
- Reliable transportation
- Senior level
- Commercial
- Paid training
- Opportunities for advancement
Quick Apply
1d
Contractor Quality Assurance/Control Supervisor - Landfill Construction/Cap Construction
Ayuda Companies —United States
- $90,000 - $120,000 a year
- Full-time
- Background check
- Construction site
- Pass drug screening
- Disability insurance
- Health insurance
Quick Apply
Quality Control Manager- Dam Project
Thalle Construction Company —United States
- Full-time
- Construction site
- Senior level
- Professional Engineer
- Paid holidays
- Disability insurance
Quick Apply

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Nuclear Supplier Quality Manager
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Associate Director - QA

Bionova Scientific LLC -
The Woodlands, TX

Apply Now

Job Details

Full-time
$150,000 - $164,000 a year
2 days ago

Qualifications

Document control experience within pharmaceutical industry
Corrective and preventive actions (CAPA)
Internal investigations
Manufacturing facility experience
Laboratory quality control records management
Quality risk management
Bioprocessing
Data-driven problem-solving
Test validation method
Senior leadership
Pharmaceutical manufacturing facility experience
Laboratory compliance and regulatory documentation

Full Job Description

The Associate Director of QA is a driven, resourceful, and solution-oriented leader for Bionova Scientific's pDNA site in The Woodlands, Texas. This position will provide site-level Quality leadership and oversight for GMP pDNA manufacturing, QC laboratory operations, and the site's Quality Systems.

The ideal candidate will bring strong cGMP, microbial/biologics manufacturing, laboratory Quality, and Quality Systems experience together with a practical CDMO mindset. This leader will partner closely with Manufacturing, QC, MSAT, Facilities/Engineering, Supply Chain, and Program Management to enable compliant, predictable, and timely execution of pDNA client and internal programs.

The role requires proactive identification of Quality and release-critical dependencies, clear and timely risk communication, consistent application of regulatory and internal requirements, and the ability to develop compliant, risk-based paths forward. Success will depend on maintaining inspection readiness, strengthening the site's Quality Systems, building cross-functional trust, and integrating Quality requirements early into program planning, technology transfer, manufacturing, testing, and disposition.

Location: Woodlands, TX

Essential Duties and Responsibilities:

Provide day-to-day leadership and oversight for QA Operations supporting GMP pDNA Manufacturing and QC, together with site Quality Systems.
Demonstrated experience leading and hosting client, corporate, and regulatory audits/inspections including preparation, front-room/back-room coordination, response development, and management of audit observations through closure.
Maintain regular and transparent communication with the Site Head through scheduled 1:1s, leadership meetings, presentations, and periodic Quality updates, providing clear visibility to Quality System health, compliance risks, audit/inspection readiness, Manufacturing and QC issues, release-critical dependencies, and emerging concerns.
Develop and present concise, data-driven Quality updates and presentations for Site Leadership as needed. Escalate urgent or high-impact Quality risks promptly to ensure timely awareness and cross-functional action.
Provide appropriate Quality oversight and guidance for GMP activities while working collaboratively across functions to support compliant and effective execution.
Provide QA presence and support on the manufacturing floor, including real-time assessment of GMP events, documentation practices, deviations, line clearance, material status, and adherence to approved procedures and batch records.
Provide QA oversight of QC laboratory operations supporting pDNA, including sample management, specifications, analytical method qualification/validation, data review, laboratory investigations, OOS/OOT events, reference standards, stability, and release testing.
Ensure Manufacturing and QC readiness requirements are identified and resolved before execution, testing, or disposition activities become schedule-critical.
Ensure release-critical Quality requirements and cross-functional interdependencies are identified early, assessed for risk and criticality, assigned clear ownership, and communicated through project and site governance.
Review and approve, as applicable, specifications, master and executed batch records, SOPs, protocols, reports, deviations, CAPAs, change controls/MOCs, investigations, method qualification/validation documentation, facility/equipment qualification documentation, and other GMP records.
Support disposition and release activities for raw materials, master/working cell banks, intermediates, pDNA drug substance/product, reference standards, and other applicable GMP materials in accordance with approved specifications, procedures, and Quality Agreements.
Lead and continuously improve site Quality Systems, including document control, deviations, CAPA, change control, training, risk management, supplier quality, audit management, and Quality Management Review.
Lead the evaluation of data integrity practices and drive the assessment and implementation of digital Quality and laboratory systems, including LIMS and/or new or enhanced electronic QMS platforms.* Ensure Quality requirements are applied consistently and that regulatory requirements, internal Quality System/procedural requirements, client requirements, and risk-based Quality decisions are clearly understood, documented, and communicated.
Drive timely investigation and closure of deviations, CAPAs, change controls, OOS/OOT events, and other Quality records using scientifically sound root cause analysis and effective corrective and preventive actions.
Partner with PM, Manufacturing and QC leadership to establish and monitor Quality KPIs that provide early visibility to compliance, investigation, testing, release, and execution risks.
Partner with Process/Analytical Development and MSAT to ensure appropriate transfer of pDNA processes, analytical methods, specifications, controls, and supporting documentation into GMP Manufacturing and QC operations.
Partner with Facilities/Engineering and Validation to support qualification and lifecycle management of facilities, utilities, manufacturing equipment, laboratory equipment, cleaning processes, computerized systems, and environmental controls as applicable.
Provide Quality input during client onboarding, project planning, technology transfer, manufacturing readiness, analytical readiness, GMP campaign planning, and schedule development as required.
Serve as the site Quality escalation point for Manufacturing and QC issues, driving timely resolution collaboratively with management or independently, as appropriate based on risk and criticality.
Support development and execution of Quality Agreements and ensure client-specific Quality and release requirements are translated into site execution plans.
Lead Quality Management Review inputs and ensure meaningful trends, recurring issues, systemic risks, and improvement opportunities are escalated and acted upon.
Promote a culture in which Quality is integrated proactively into operations and program execution rather than functioning only as a final review or approval step.
Build, coach, and develop a high-performing QA team capable of supporting a growing, multi-client pDNA CDMO operation.

Working Conditions:

Requires regular presence in GMP microbial manufacturing and QC laboratory areas.
May require standing, sitting, walking, gowning, and movement through controlled manufacturing and laboratory spaces.
May require support outside normal business hours during critical manufacturing operations, testing, investigations, client activities, or inspections.
Occasional travel up to 15% may be required for client engagement, audits, training, conferences, or vendor visits.

Qualifications:

BS/MS in Biology, Microbiology, Biochemistry, Chemistry, Engineering, Pharmaceutical Sciences, or a related life science discipline; advanced degree preferred.
5 to 10 years of progressive Quality experience in biopharmaceutical, biologics, plasmid DNA, microbial manufacturing, cell and gene therapy, vaccine, or related GMP environments, including meaningful leadership responsibility.
Demonstrated experience leading or providing senior QA Operations oversight for both GMP Manufacturing and QC laboratory functions.
Strong working knowledge of 21 CFR Parts 210/211, applicable ICH guidance, EU GMP expectations, data integrity principles, and pharmaceutical Quality Systems.
Demonstrated experience with batch record review, disposition/release, deviations, CAPA, change control, OOS/OOT, specifications, investigations, validation/qualification, document control, and Quality risk management.
Experience establishing, maintaining, and improving Quality Systems in a growing, changing, or start-up GMP manufacturing organization.
Strong understanding of QC laboratory operations, analytical method lifecycle, method qualification/validation, specifications, reference standards, stability, data review, and laboratory investigations.
Experience supporting manufacturing-floor QA and making timely, risk-based Quality decisions during GMP execution.
CDMO experience strongly preferred, including experience supporting multiple client programs, Quality Agreements, competing priorities, and aggressive timelines.
Strong risk management, root cause analysis, strategic thinking, troubleshooting, and continuous improvement capabilities.
Excellent written and verbal communication skills, including the ability to translate complex Quality and regulatory issues into clear, actionable recommendations.
Authorized to legally work in the United States without visa sponsorship.

The base compensation range for this role is $150,000-$164,000. Base Compensation is influenced by many factors including, but not limited to: time in the role, previous experience, skills, knowledge, performance, work requirements, internal equity, and business / economic conditions.

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quality manager jobs in willis, tx

Associate Director - QA

Nuclear Supplier Quality Manager

Quality Manager

Quality Manager - Stabil Drill

QHSE Manager

Quality Manager

Quality Manager

Quality Assurance Manager - Eurofins Drinking Water and Wastewater Central - Huntsville, TX

QA/QC Manager

FCW-SH99 JV Deputy Construction Quality Control Manager

FCW-SH99 JV - Quality Control Manager

Associate Director - QA

QA Lead, Quality Systems (Cell Therapy)(W)

Nuclear Supplier Quality Manager

Senior Water Quality Environmental Consultant (Project Manager) - TX

Janitorial Quality Assurance / Field Supervisor - Conroe & The Woodlands, TX

Janitorial Quality Assurance / Field Supervisor - Graveyard Shift (Part-time)

Contractor Quality Assurance/Control Supervisor - Landfill Construction/Cap Construction

Quality Control Manager- Dam Project

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