Quality Analyst - Fort Lauderdale Florida

Company: Aequor Technologies
Location: Fort Lauderdale, Florida
Posted On: 02/05/2025

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Job Title: Quality Analyst -Pharmaceutical Company

Location: Davie, FL

Duration: 6 Months + Extensions

2nd Shift Schedule: Monday - Friday ( 2:00pm - 10:30pm), 40 hours a week

Core Essential Skill sets candidates must have to be considered for the role:
1. Min Bachelor Degree on Engineering, Biology, Chemistry or equivalent
2. Experience with project management, process excellence
3. Pharmaceutical environment
4. Quality experience
5. GMP experience
6. Manufacturing experience
7. Experience Microsoft PowerPoint, Excel

Position Summary:

This position is primarily responsible to support Projects under Quality Organization. The projects are related but not limited to the following: Batch Record Review Process Simplification, Quality KPI-RFT Metrics Acquisition and Evaluation/Reporting, Standardization of the Deviations Tracking System, Doc Control Off load.
The main responsibility of this position is to identify areas for simplification while looking for efficiencies on Quality processes. The temporary resource will apply project management skills, DMAIC tools and operational excellence tools such as 5S, Value Stream mapping, and evaluation of wastes and suggest new potential process maps based on inputs of the areas.
Also, coordinate meetings, conduct data gathering and evaluate results.

Essential Areas of Responsibility:
1. Responsible to collect data through observation of tasks, duties
2. Develop current state of process map of the area identified.
3. Coordinate meetings for the data/process evaluation
4. Identify areas of opportunities and discuss with the area manager and QLT.
5. Develop proposal new state for the process evaluated.
6. Develop plan, establish the support required for procedures updates and training required
7. Identify metrics to be used to monitor
8. Execute plan

Position Requirements:
Any equivalent combination of education, training and or experience that fulfills the requirements of the position will be considered.
Education/Certification/Experience:
1. Bachelor Degree on Engineering, Biology, Chemistry or equivalent. from an accredited college or university, with a minimum of 1-3 years relevant progressive cGMP compliance experience within the manufacturing/pharmaceutical industry.
2. Experience with project management, process excellence, pharmaceutical environment More...

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