2mo
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Supervisor, Quality control (TAS) (Sunrise, FL, US, 33325)
Sunrise, Florida, United States
OnsiteFull Time
5+ YOESupervise QC inspectors, analyze trends, implement CAPA, ensure ISO13485/21 CFR820 compliance.
Sampling plans, CAPA system, ISO 13485, 21 CFR Part 820
2mo
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QMS Manager
Pembroke Pines, Florida, United States
OnsiteFull Time
6+ YOE12+ years in quality within regulated technical fields; QMS design and ISO 9001; audits and CAPA; risk management; document control; ASQ preferred.
QMS, ISO 9001, CAPA, Document Management
1d
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Quality Assurance Specialist
Boca Raton, Florida, United States
OnsiteFull Time
Experience in regulated manufacturing with strong knowledge of GMP, QMS, CAPA, deviations, document control and SOPs; analytical skills and English proficiency; bachelor's degree preferred.
eQMS
3w
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Lead Quality Technician (FL, Miramar)
Miramar, Florida, United States
OnsiteFull Time
Senior quality role overseeing inspections, testing, non-conformance management, CAPA, calibration, mentoring technicians, and participating in continuous improvement in an LSR injection molding facility.
calipers, micrometers, optical comparator, coordinate measuring machine (CMM), QMS, Six Sigma, Lean
3w
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Senior Project Engineer
Boca Raton, Florida, United States
OnsiteFull Time
10+ YOE10+ years engineering experience in cGMP pharmaceutical/biological manufacturing; project management, commissioning, P&ID review, load calculations, CAPA documentation, strong technical writing and Microsoft Office skills.
Microsoft Word, Microsoft Excel, Microsoft Project
1w
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Quality Systems & Compliance Manager
Fort Lauderdale, Florida, United States
$90k-$120k/yr HybridFull Time
3+ YOE3–7 years quality or manufacturing experience, ISO 9001:2015 experience, strong technical writing, document control, audit and CAPA skills, ability to interpret technical drawings, Microsoft Office proficiency.
Microsoft Office Suite, SharePoint, Microsoft Power Platform, ERP
1mo
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Commissioning and Qualification Engineer
Tamarac or Miramar
$85k-$95k/yr OnsiteFull Time
2+ YOEBachelor's in engineering (Master's preferred), 2+ years commissioning and qualification experience in pharmaceutical/medical device, GMP/CFR/ICH knowledge, statistics/DoE, CAPA and project management, proficient with Word/Excel/Project/Minitab.
Microsoft Word, Microsoft Excel, Microsoft Project, Minitab
3mo
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Quality Assurance Engineer II
Miami, Florida, United States
OnsiteFull Time
3+ YOEBachelor’s in engineering or related technical field; 3-4 years in engineering or quality; knowledge of FDA, AATB, ISO 13484, cGTP; experience in tissue banking/pharma/biologics; CAPA experience; strong software skills.
Microsoft Project, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1mo
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Engineer II, Quality
Miami, Florida, United States
$83k-$104k/yr OnsiteFull Time
BS in engineering/biomedical/biological sciences; knowledge of electronic QMS, GMP/GTP, quality tools (FMEA, DMAIC, 5-Whys), ERP and MS Office; support CAPA, investigations, change control, audits, and CoA review.
6Ms, 5-Why's, FMEA, DMAIC, Cause and Effect Diagrams, Process Mapping, Electronic Quality Management Systems, ERP, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
5d
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Product Quality Engineer
Atlanta or Houston or Miami or Tysons or United States
RemoteFull Time
5+ YOEBachelor's in engineering,5+ years quality engineering in energy/power,experience leading FATs for electrical equipment,knowledge of ISO 9001/NCR/RCA/CAPA,ability to read electrical/civil drawings,and willingness to travel up to 75%.
1d
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Quality Systems and Testing Specialist
Fort Lauderdale, Florida, United States
HybridFull Time
2+ YOEBachelor's in life sciences,2+ years QA/QC or lab experience in supplements/pharma/food,knowledge of 21CFR111,GMP,GDP,data integrity,OOS/OOT/CAPA,analytical methods (HPLC,ICP-MS,FTIR),and Microsoft Office proficiency.
HPLC, ICP-MS, FTIR, Microsoft Office
2mo
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Sr. QA Specialist, Operations
Plantation, Florida, United States
OnsiteFull Time
5+ YOESenior QA on-floor role ensuring GMP compliance; 5-8 years GMP, cGMP, aseptic manufacturing, data integrity; high school diploma required; associate or bachelor's preferred.
GMP systems, Aseptic manufacturing, CAPA, SOPs, NetSuite, Documentation control, Batch records review
2mo
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Quality Assurance Director
Miami, Florida, United States
OnsiteFull Time
10+ YOE5+ Mgmt10+ years in pharma/clinical industry; leading QA, GMP/GCP, audits; bilingual Spanish preferred; FDA/Regulatory inspections experience.
GCP, FDA CFR 21 Part 11, CAPA, QMS, eQMS, Clinical Trial Management Systems, MS Word, MS Excel
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