Demo

Quality Assurance Specialist

Radiant
Fort Lauderdale, FL Temporary
POSTED ON 4/5/2025
AVAILABLE BEFORE 5/3/2025

Shift Schedule : Monday – Friday 2 : 00pm - 10 : 30pm, Flexibility to work one or two weekends during the month either in the morning or afternoon as needed by the client.

Duration : 6 months with possibility to extend

Temp to Perm : Possibility based on openings and performance

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.

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

1. Skills / Knowledge / Abilities :

  • Establishing and maintaining cooperative working relationships with others.
  • Reading, understanding, interpreting and complying with current Company policies and procedures including safety rules and regulations.
  • Communicating clearly and concisely, both orally and in writing.
  • Operating personal computer and database software.
  • Handling multiple projects, duties and assignments.
  • Quality Assurance methods and procedures.
  • Related business, scientific and personal computer hardware and software applications in area of assignment.

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