139 fda jobs at 57 companies in Dayton, TX
3mo
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Senior Supplier Quality Engineer
Houston, Texas, United States
$110k-$120k/yr OnsiteFull Time
8+ YOEBachelor's degree in engineering; 8+ years quality/manufacturing engineering experience; regulated FDA medical device environment preferred; strong quality and project management skills.
Quality Management System (QMS), ISO 13485, MDSAP, FDA regulations
1mo
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Center Director 1
Pasadena, Texas, United States
OnsiteFull Time
Leadership role overseeing donation center operations, regulatory compliance (FDA/OSHA/CLIA/GMP), quality and safety programs, staff management, training, and achievement of production and financial targets; bachelor’s preferred.
FDA, OSHA, CLIA, GMP, CAPA
1mo
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QC Scientist, I - Method Validation(W)
The Woodlands, Texas, United States
OnsiteFull Time
4+ YOEB.S. in a life science, 4+ years biotech/pharma/cell therapy experience, hands-on mammalian cell culture and analytical method qualification/validation experience, flow cytometry/ELISA/PCR familiarity, knowledge of cGMP/ICH/FDA.
flow cytometry, ELISA, PCR, ALCOA+, GMP, GDP, ICH, FDA
1mo
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Associate Quality Engineer
Houston, Texas, United States
$51k-$101k/yr OnsiteFull Time
0+ YOEBachelor's in engineering or technical field (or equivalent), 0-2+ years engineering experience, knowledge of FDA/GMP/ISO 13485 & 14971, use of quality tools, Six Sigma/Lean experience preferred, strong communication and statistical/data analysis skills.
FDA, GMP, ISO 13485, ISO 14971, Six Sigma, Lean Manufacturing, QMS, EMS, CAPA
1mo
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Associate Quality Engineer
Houston, Texas, United States
$51k-$101k/yr OnsiteFull Time
0+ YOEBachelor's in engineering or technical field (or equivalent), 0–2+ years engineering experience, knowledge of FDA/GMP/ISO standards, experience with quality tools, statistical/data analysis, Six Sigma/Lean experience preferred, strong communication and project skills.
FDA, GMP, ISO 13485, ISO 14971, Six Sigma, Lean Manufacturing, QMS, EMS
1d
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Director, Clinical Research Regulatory Affairs
Houston, Texas, United States
$147k-$220k/yr RemoteFull Time
8+ YOE2+ MgmtBachelor's in life sciences/pharmacy/medicine required, Master’s preferred; 8+ years regulatory affairs experience with FDA submissions, 2+ years lead project management, RAC preferred, strong FDA/ICH/GCP knowledge.
1mo
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Regulatory Compliance Specialist - Transplant Center
Houston, Texas, United States
OnsiteFull Time
2+ YOEBachelor's degree, 2 years clinical research or regulatory compliance experience in academic/FDA-regulated settings; knowledge of IRB/FDA/GCP, strong communication, data entry, and process improvement skills; Excel/Word/PowerPoint proficiency.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint
2w
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Director, Clinical Research Regulatory Affairs in United States, Texas, Houston, Houston (TX Med Ctr)
Houston, Texas, United States
$147k-$220k/yr RemoteFull Time
8+ YOE2+ MgmtBachelor's required, Master's preferred; 8+ years regulatory affairs experience with FDA submissions and oncology research; 2+ years lead project management; IND/IDE experience preferred; RAC preferred; strong FDA, ICH/GCP knowledge.
2mo
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Clinical Research Chart QA/Auditor
The Woodlands, Texas, United States
$60-$100/hr OnsiteContract
5+ YOE5+ years QA auditing in clinical research; FDA inspections; ICH-GCP; strong documentation and communication.
FDA inspections, ICH-GCP, 21 CFR Part 11, CAPAs, Audit reporting
3w
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Biolife - Licensed Practical Nurse (LPN)
Humble, Texas, United States
$24-$33/hr OnsiteFull Time
2+ YOECurrent LPN/LVN license in Texas, CPR and AED certification, basic IV therapy, FDA BioLife training, 2 years clinical experience.
1d
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Assistant Plant Manager
Houston, Texas, United States
OnsiteFull Time
3+ YOE2+ MgmtOversee plant operations, manage production and staff, ensure regulatory compliance (FDA/DOT/OSHA/EPA), and support inventory, maintenance, and quality programs.
SAP, Power BI
2w
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Quality Assurance Specialist
Houston, Texas, United States
OnsiteFull Time
5+ YOEBachelors in science required. Experience with GMP, investigations, CAPA, audits, quality metrics, and MasterControl; 5+ years conducting investigations in FDA-regulated environments preferred.
MasterControl, eQMS
2mo
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Clinical Research Site Director
Boston or Houston
OnsiteFull Time
8+ YOE5+ Mgmt8+ years clinical research experience; 5+ years managing multiple trials and teams; strong knowledge of FDA regulations, ICH-GCP, and site operations.
EDC, IVRS, Electronic Data Capture, SOPs
3mo
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QA and Food Safety Manager (Missouri City, TX, US, 77489)
Missouri City, Texas, United States
$97k-$145k/yr OnsiteFull Time
5+ YOE5+ Mgmt5 years supervisory experience in food manufacturing; BA/BS in related field; knowledge of GMP, HACCP, FDA regulations; strong analytical and leadership skills.
Excel
2mo
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Senior Process Engineer
Stafford, Texas, United States
OnsiteFull Time
7+ YOE7+ years of process engineering in regulated manufacturing; medical device experience preferred; strong FDA QSR/ISO 13485 knowledge; root cause analysis experience.
2w
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CMA, LVN or RN - Kingwood
Kingwood, Texas, United States
OnsiteFull Time
1+ YOECMA certification or LVN or RN license valid in Texas, 1–2 years medical experience, knowledge of OSHA/FDA/HIPAA, skilled charting, and strong communication.
1mo
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Process Engineer
Houston, Texas, United States
OnsiteFull Time
5+ YOEBachelor's in Chemical Engineering, over 5 years process engineering experience in cosmetics, proficiency with MS Office, knowledge of GMP/FDA, strong analytical and communication skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1d
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Sub Investigator (NP) (4067)
Houston, Texas, United States
OnsiteFull Time
Current clinical licensure (NP or PA), clinical research and nursing experience, knowledge of FDA/GCP/ICH, ability to perform exams, EKGs, phlebotomy, and document study procedures.
2mo
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Senior Clinical Research Associate
Remote or Houston
$120k-$135k/yr RemoteFull Time
4+ YOEBS life sciences or nursing; 4+ years on-site monitoring; strong knowledge of ICH-GCP, FDA/EMA; site management and trial documentation; CTMS/eTMF proficiency.
CTMS, eTMF, Microsoft Office
2w
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Research Coordinator I - Internal Medicine, Critical Care (Bilingual)
Houston, Texas, United States
OnsiteFull Time
Bachelor's degree required; detail-oriented coordinator experienced in participant recruitment, informed consent, data collection, and regulatory compliance (GCP/HIPAA/FDA/IRB knowledge preferred).