USA - Quality Assurance Associate III (IT) (contract)

Job Summary

Join Sanofi's contingent workforce program, FLEXT Direct, as a Quality Assurance Associate III

for a 12-month contract. This contract position is responsible for various aspects of support for the Stability program including the organization of samples and documentation related to the room temperature stability program. This position will be guided on support-related tasks such as retaining sample data entry, APR database data entry, sample labeling, and sample collection and delivery. In addition, this position also supports any duties of the Stability Technician II and the Stability Data Analyst II roles as needed.

Role Specific Responsibilities

Stability Technician duties fall under the scope of any data or documentation that relates to the room temperature stability or accelerated stability process.

• Labeling, storage and organization of room-temperature or accelerated stability samples and documentation.
• Enter and/or verify analytical and water data in the APR database.
• Enter and/or verify stability data in Novatek.
• Provide support for the file sample process by logging samples in SAP.
• Filling of room temperature stability results.
• Logging of samples for the laboratory.
• Perform visual inspection of retain samples.
• Supports Stability Technician II and Stability Data Analyst II with other department related duties as assigned (e.g. – lab clean up)
  
  
  

Interfaces

• Quality Assurance
• Quality Control (Analytical and Microbiology)
• CHC Research and Development
• Analytical Research and Development
• Analytical Quality Assurance
• Complaints
  
  
  

Competencies

• Must be organized and detail oriented
• Project management
• Technical writing
• Statistical Analysis
• Ability to adapt to a changing environment and adjust flexibly
• Strong verbal and written communication skills required
  
  
  

This description is representative but not inclusive of all position responsibilities. Associate may be asked to complete tasks not listed within the contents of this document, but that are relative to the goals of the business.

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Qualifications

Education: A.S. Degree in Chemistry or closely related field.

Experience: 3 years of GMP related experience or equivalent.

Professional Skills: Basic computer skills, technical writing skills, attention to detail, and good communication skills.

Role Specific Competencies: Knowledge of GMPs. Heavy Data Entry. This position requires extensive use of computer equipment. Must have a demonstrated proficiency in Microsoft business software including Access, Excel, Word, and Outlook.

Special Requirements: Position is 100% onsite and based in Chattanooga, Tennessee at Sanofi CHC’s Corporate office