61 fda jobs at 33 companies in Bristol, CT
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Clinical Research Coordinator 2
New Haven, Connecticut, United States
$65k-$101k/yr OnsiteFull Time
2+ YOECoordinate clinical trials; manage screening, eligibility, recruitment; ensure compliance with GCP, FDA, HIPAA; independent multi-study management; strong communication.
GCP, FDA Regulations, HIPAA, EMR, Clinical Trial Management Systems
1mo
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Quality Engineer (Bridgeport, CT, US, 06610-0156)
Bridgeport, Connecticut, United States
OnsiteFull Time
3+ YOEBachelor's in engineering, 3+ years quality experience with metrology/CMM, GD&T, SPC/DOE, ISO and FDA QSR knowledge, blueprint reading, statistical analysis, and ability to lead inspections and corrective actions.
CMM, optical comparators, micrometers, calipers, gage blocks, pin gages, Gage R&R, GD&T, DOE, SPC, ISO, FDA, ECNs, SCRs, Material Review Board (MRB)
2mo
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Quality Management System (QMS) Engineer
Torrington, Connecticut, United States
$70k-$100k/yr OnsiteFull Time
3+ YOELead and maintain QMS, CAPA, NCR, audits; ensure FDA/ISO compliance in regulated medical device manufacturing.
eQMS, CAPA system, document control software
2mo
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Operations Supervisor
Windsor, Connecticut, United States
OnsiteFull Time
3+ YOE3+ MgmtBachelor’s degree + 3+ years distribution/warehouse management; 3+ years supervisory; pharma warehousing and HazMat preferred; FDA/cGMP familiarity
Tecsys Elite, MQ1, Outlook, Excel, PowerPoint, TECSYS, UKG
3w
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Principal Microbiologist
Stamford or Trumbull
$110k-$120k/yr OnsiteFull Time
10+ YOE10+ years industry microbiology experience with preservation, antibacterial product development, regulatory interpretation (FDA), complex study design, manufacturing microbiology, and leadership.
2mo
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Compounding Inspector
New London, Connecticut, United States
$18-$20/hr OnsiteFull Time
High school diploma; ability to work 3rd shift; knowledge of cGMP/FDA/GLP; basic lab skills; English proficiency; strong record-keeping.
3w
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Product Development Manager (5703)
Windsor Locks, Connecticut, United States
OnsiteFull Time
Lead product development for medical films and nonwovens, oversee design transfers, manage projects and trials, understand film chemistry and FDA/ISO awareness, and travel as needed.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Microsoft Teams
1w
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Analytical Chemistry Quality Cooridinator
Trumbull, Connecticut, United States
$85k-$95k/yr OnsiteFull Time
UnileverLondon Stock Exchange: ULVR: Manufactures and distributes food, home, and personal care products.
3+ YOEBachelors in science (chemistry preferred) with 5+ years or Masters with 3+ years; QC lab experience, knowledge of FDA/HC/ICH, LIMS, statistical analysis, and chromatographic techniques.
Laboratory Information Management System (LIMS), LabVantage, Power BI, Microsoft Excel, JMP, SPSS, Python, R, Matlab, HPLC, GC, ChemStation, Open Lab, Empower
2w
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Prin Regulatory Affairs Spec
North Haven or Mansfield or Mounds View or Boston or Lafayette
$120k-$180k/yr OnsiteFull Time
7+ YOEBachelor's degree and 7+ years regulatory experience (or advanced degree with 5+ years). Experience with 510(k), FDA interactions, international registrations, labeling and promotional material review.
19h
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Risk Management Quality Engineer I - New Product Development (Surgical)
North Haven, Connecticut, United States
$66k-$100k/yr OnsiteFull Time
Bachelors in engineering or related field; experience with risk management, design controls, DFMEA, post-market surveillance, and regulatory compliance (FDA/ISO). Strong written/verbal skills.
Minitab, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
2mo
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ERP Operations Analyst
Bethel, Connecticut, United States
$78k-$113k/yr OnsiteFull Time
7+ YOE5+ Mgmt7+ years manufacturing; 5+ years in manufacturing/inventory management; lean tools knowledge; ERP experience; FDA/GMP/ISO 13485 knowledge; strong communication and analytical skills.
Epicor ERP, QAD, Microsoft Office
3w
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Manufacturing Supervisor
Canaan, Connecticut, United States
OnsiteFull Time
5+ YOEBachelor's degree or equivalent and 5+ years relevant experience; leadership and coaching skills; knowledge of safety, quality, FDA/GMP/ISO/OSHA; proficiency with SAP, MES and Microsoft Office.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, SAP, MES
1mo
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Engineer I, Manufacturing
Southington, Connecticut, United States
OnsiteFull Time
2+ YOEBachelor's in Engineering/Technology/STEM, 2 years' medical device or engineering experience, knowledge of injection molding, automation, Six-Sigma methods, FDA QSR, SolidWorks, and technical writing.
SolidWorks
1mo
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Part-time- temporary Food Inspector (CT, South Windsor)
South Windsor, Connecticut, United States
$35/hr FieldPart Time, Temporary
Conduct inspections of licensed food establishments to ensure compliance with the FDA Food Code and local health ordinances; flexible hours including evenings/weekends; mileage reimbursed for travel between inspections.
23h
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Clinical Research Coordinator
Orange, Connecticut, United States
$65k-$80k/yr OnsiteFull Time
Coordinate clinical trial activities, manage informed consent and source documentation, report adverse events, ensure protocol and regulatory compliance (FDA/ICH/HIPAA/GCP), and support participant safety.
interactive web response systems (IWRS)
1w
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Office Manager
Trumbull, Connecticut, United States
OnsiteFull Time
5+ YOE5+ Mgmt5+ years supervisory experience in healthcare, HS/GED required, college degree preferred; knowledge of FDA/ACR/MQSA standards; ability to monitor all shifts and manage radiology operations.
2mo
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Copy of Quality Inspector
Shelton, Connecticut, United States
OnsiteFull Time
3+ YOEInspect incoming, in-process, and final goods; read blueprints; 3-5 years in quality/manufacturing; ISO 13485 and FDA GMP knowledge; lift up to 50 lbs; proficient with MS Office.
Calipers, Optical comparators, Microsoft Office Suite
1mo
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Process Development Technician I
Enfield, Connecticut, United States
OnsiteFull Time
3+ YOEHigh school/GED required, 3+ years in engineering/manufacturing for medical devices, knowledge of FDA cGMP and ISO 9001/13485, fluent English. Familiarity with Pro-E/CREO or SolidWorks and DMAIC is a plus.
Pro-E/CREO, SolidWorks
4w
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Supplier Quality Engineer Lead
Trumbull or Livingston
$120k-$150k/yr OnsiteFull Time
10+ YOELead supplier quality strategy and governance in regulated medical device environments; expertise in FDA QSR, ISO 13485, EU MDR, ISO 14971, audits, CAPA/SCAR, RCA/FMEA, and supplier development.
Microsoft Office, Minitab, ERP systems, eQMS platforms
2mo
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Clinical Research Nurse 2
New Haven, Connecticut, United States
$68k-$121k/yr HybridFull Time
3+ YOEGraduate of an accredited nursing program with a minimum of 3 years related nursing or clinical research nursing experience; strong clinical, analytical, organizational skills; knowledge of FDA/ICH/GCP; Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Clinical Trials Management Systems (CTMS), Beacon
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