Qa Jobs in Davie, FL
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Qa • davie fl
QA Specialist
ActalentFort Lauderdale, Florida, USAQA Inspector
5th HQMiramar, FLQA Manual Tester
SherlockTalentFt lauderdaleSr. QA Manager Enterprise Data Services
Southern Glazer's Wine and Spirits, LLCHollywood, FL, United States- Promoted
QA Manager
United IT Solutions, Inc.Fort Lauderdale, FL, USQA Engineer
QuantfuryFort Lauderdale, FL, United States- New!
QA Engineer
INSPYR SolutionsMiramar, FLQA Automation EngineerGravity IT Resources
Gravity IT ResourcesMorrisville, Florida- Promoted
Staff QA / Supply Chain Test Engineer-Blue Yonder
Southern Glazer's Wine & SpiritsMiramar, FL, United States- Promoted
BSA QA Analyst
AmerantbankMiramar, FL, USSr. QA Manager Enterprise Data Services
Southern Glazer's Wine & Spirits of AmericaMiramar, FL, United StatesWH / QA Inbound / Outbound Inspector
ALOIA AEROSPACE INCDania Beach, Florida, USSr. QA Manager Enterprise Data Services
Southern Glazer’s Wine & SpiritsMiramar, FL, USQA and BA Training and Placement for OPT / CPT, F1 / L2 / GC visa holders and Citizens.
IT ExcelColumbia County, FLQA Test Engineer
General DynamicsFort Lauderdale, FL, United StatesSr. QA Manager Enterprise Data Services
Southern Glazer's Wine and SpiritsHollywood, FL, United StatesQA Specialist
ActalentFort Lauderdale, Florida, USA- Full-time
Actalent is Hiring a QA Specialist
Job Description
The position involves reviewing all analytical reports and raw and electronic data from CMC, including various materials and equipment calibration. The role requires informing the CMC Manager and QA when tests are not within specified limits to take appropriate actions.
Responsibilities
- Ensure analytical data meets company standards and regulatory requirements.
- Review test results and raw data for various materials and stability samples, including assays, chromatographic purity, content uniformity, particle size distribution, density, and water determination.
- Check laboratory notebooks and associated documents for correctness and verify all reagents, standards, and equipment used.
- Review raw data for audit trails and instrument logs on cGMP instrumentation and equipment.
- Review validation and method optimization reports.
- Ensure chemists follow SOPs and cGMP regulations and use correct methods for each product.
- Promptly review notebooks and sign off on all analytical test results and reports.
- Analyze and interpret results in written and oral formats.
- Work with analysts for document corrections and provide guidance on laboratory notebook documentation requirements.
- Follow SOPs and Safety Guidelines to ensure compliance with cGMP environment and Safety Practices.
- Provide support during regulatory and internal audits.
- Review Laboratory Incidents, OOS, OOT, and OOE investigations.
- Perform additional tasks as assigned by the QA supervisor.
Essential Skills
Additional Skills & Qualifications
Work Environment
This is an on-site role from Monday-Friday / both first and second shifts are available. The position generally involves standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking, and hearing. Occasionally, bending, kneeling, crouching, stooping, and crawling may be required.
Pay and Benefits
The pay range for this position is $32.00 - $35.00 / hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following :
Workplace Type
This is a fully onsite position in Fort Lauderdale,FL.
Application Deadline
This position is anticipated to close on Jul 22, 2025.