19 capa jobs at 12 companies in Lake Jackson, TX
3w
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Quality Control Inspector I
Stafford, Texas, United States
OnsiteFull Time
0+ YOEPerform visual, dimensional, mechanical and functional inspections; document results; identify and report nonconformances; follow procedures and support CAPA and audits.
Microsoft Excel, Microsoft Word, Microsoft Teams, Outlook, PowerPoint, calipers, micrometers, gauges, vision systems
4w
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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
3w
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Senior Manufacturing Associate
Stafford, Texas, United States
OnsiteFull Time
4+ YOEAssociate's or Bachelor's in a scientific field, 4+ years GMP manufacturing experience, aseptic/cleanroom experience, ALCOA++/cGDocP documentation, deviation/CAPA investigations, and mentoring experience.
ALCOA++, cGDocP, IQ/OQ/PQ
2d
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Quality Assurance Specialist IV
Pearland, Texas, United States
OnsiteFull Time
5+ YOEBachelor's degree in a scientific discipline and 5+ years of GMP quality assurance experience required, including manufacturing support, deviations, investigations, CAPAs, change controls, aseptic processing, and cleanroom operations.
TrackWise, Microsoft Office, Documentum, SAP, LIMS
1w
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Facilities Manager
Missouri City, Texas, United States
$100k-$106k/yr OnsiteFull Time
7+ YOERequires 7+ years managing facilities or engineering in regulated environments, cleanroom certification experience, commissioning, BMS/EMS monitoring, SOPs, deviation/CAPA, change control, and listed safety certifications.
BMS, EMS, CMMS, ISO 14644, USP <797>, USP <800>, NEBB CPT, NSF/ANSI 49, BCxA CCP, AABC CxA, IFMA CFM, SMRP CMRP
1mo
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Quality Assurance Specialist
Sugar Land, Texas, United States
$60k-$66k/yr OnsiteFull Time
3+ YOE3+ years QA experience in manufacturing or consumer products; knowledge of ISO 9001, CAPA, document control, calibration, root cause analysis, retail compliance portals, laboratory testing, and corrective actions.
Monday.com, Walmart Retail Link, Costco systems, Tracegains, Mars repositories, ISO 9001, FMEA, SPC, Lean Six Sigma
3w
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Quality Assurance Specialist
Sugar Land, Texas, United States
OnsiteFull Time
2+ YOE2+ years QA experience in engineering, proficiency with CAPA/NCR/FAI, ability to interpret mechanical drawings, perform inspections, conduct root-cause analysis, and ensure compliance with ISO 9001/AS9100/ITAR.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Teams
1w
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QA/Compliance Pharmacist
Missouri City, Texas, United States
OnsiteFull Time
5+ YOEActive Texas pharmacist license, BCSCP, current gloved fingertip and media-fill qualification, and 5+ years of sterile compounding experience owning quality systems, regulatory compliance, audits, SOPs, deviations, and CAPA.
USP <795>, USP <797>, USP <800>, DEA, HIPAA, FDA, Microsoft?
2mo
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Senior Operational Quality Assurance Specialist
Stafford, Texas, United States
OnsiteFull Time
4+ YOEBachelor's in relevant science, 4+ years QA experience in biotech/pharma with batch release and cGMP/GCP experience; experience reviewing batch records, managing deviations/CAPA, and supporting audits and documentation control.
1mo
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Quality Assurance Supervisor - Night Shift
Pearland, Texas, United States
OnsiteFull Time
5+ YOE5+ years QA experience in GMP-regulated environments, Bachelor's in a scientific discipline required, supervisory experience, strong cGMP and quality systems knowledge, investigations/CAPA/change control experience, cleanroom/gowning experience.
1mo
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AVP Laboratory Affairs
Houston, Texas, United States
OnsiteFull Time
10+ YOEBachelor's in a scientific discipline, 10+ years clinical lab/quality/regulatory experience, 5+ years molecular diagnostics (NGS), CLIA/CAP/FDA/OSHA experience, audit and RCA/CAPA expertise, strong analytical and communication skills.
1w
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Senior Quality Assurance Manager
Webster, Texas, United States
$95k-$115k/yr OnsiteFull Time
University degree in life sciences/pharmacy/medicine, several years QA experience in clinical trials, strong knowledge of GCP/ICH/FDA, audit/CAPA/risk/change/SOP management, training experience, willingness to travel internationally.
eQMS
1mo
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Quality Assurance Specialist II - 2nd Shift
Pearland or Houston
OnsiteFull Time
0+ YOEBachelor's in a scientific discipline required; 0–4 years QA/QC or GMP manufacturing experience; working knowledge of cGMP/GDP; experience with batch records, deviations, CAPA, and documentation systems; comfortable with cleanroom Level 3 gowning.
3w
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Quality Engineer - Complaint Handling (Onsite)
Pearland, Texas, United States
OnsiteFull Time
1+ YOE1+ year medical device quality or complaint handling experience; bachelor\u0002s in engineering or science; knowledge of FDA 21 CFR 803/820, EU MDR, ISO 13485; complaint investigations, CAPA, root cause analysis, regulatory reporting.
eQMS
2mo
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Quality Engineer
Houston or Pearland
OnsiteFull Time
5+ YOE5+ years quality engineering in manufacturing, experience with root cause/CAPA and audits, knowledge of ISO 9001/QMS, proficiency with ERP and Microsoft Excel; Power BI/SQL and turbomachinery experience preferred. Bachelor's in mechanical/industrial engineering required or equivalent experience.
ERP, Microsoft Excel, Power BI, SQL, QMS, GD&T
2mo
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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
1d
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Facilities Engineer II
Houston or Stafford
OnsiteFull Time
5+ YOEBachelor's degree in engineering or biotechnology and 5+ years of pharmaceutical or biotech engineering experience in a GxP-regulated manufacturing or laboratory environment.
Quality Management Systems (QMS), CAPA, Change Controls, Deviations, OOS, OOT, 21 CFR Part 11, 21 CFR Part 210, 21 CFR Part 211, EU Annex 1, USP, SOPs, IQ, OQ, PQ, URS
1d
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Validation Engineer II
Stafford or Houston
OnsiteFull Time
5+ YOEBachelor’s degree in science, engineering, or related field and 5+ years in pharmaceutical or biotechnology industry; GxP, validation, quality systems, documentation, and regulatory experience preferred.
GxP, 21 CFR Part 11, 21 CFR Part 210, 21 CFR Part 211, GAMP 5, USP, CAPA, Quality Management Systems, Computer Systems Validation
1d
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Senior Facilities Engineering Manager
Stafford or Houston
OnsiteFull Time
7+ YOE5+ MgmtBachelor's degree in engineering, 7+ years in pharmaceutical or biotech engineering in GxP manufacturing or laboratory settings, and 5+ years leading teams; validation and regulated-environment expertise required.
CMMS, BMS/EMS, digital maintenance systems, HVAC, IQ/OQ/PQ, CSV, USP, QMS, CAPAs, KPIs