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QA​/QC Specialist

Job in Chattanooga, Hamilton County, Tennessee, 37404, USA
Listing for: Adecco US, Inc.
Full Time position
Listed on 2026-06-08
Job specializations:
  • Quality Assurance - QA/QC
    Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager, Quality Engineering
  • Manufacturing / Production
    QA Specialist / Manager, Quality Engineering
Job Description & How to Apply Below
** About the Role*
* A Chattanooga-based manufacturer specializing in personal care products, cosmetics, and nutritional supplements is seeking a  
** Quality Assurance & Quality Control Specialist
** to join its on-site operations. This organization supports both established and emerging brands through integrated product development, manufacturing, and quality systems.

** Position Overview*
* This full-time, on-site role focuses on supporting quality activities across regulated manufacturing operations. The specialist will play a key role in maintaining compliance, overseeing production quality, managing documentation, and contributing to continuous improvement efforts.

Working cross-functionally with production, R&D, and leadership teams, this individual will help identify risks, resolve quality concerns, and ensure adherence to internal standards and regulatory requirements.

** Key Responsibilities*
* + Assist with daily QA/QC processes within manufacturing operations

+ Review batch records, production documentation, and quality data for accuracy and compliance

+ Perform inspections of raw materials, packaging components, and finished goods

+ Monitor production and packaging activities to ensure quality standards are met

+ Maintain and update quality systems, documentation, and procedures

+ Support investigations, corrective actions, and audit readiness

+ Coordinate product testing with third-party laboratories

+ Communicate quality issues and contribute to timely resolution efforts

** Qualifications*
* + Minimum of 2 years of experience in a QA/QC role within a regulated manufacturing environment

+ Understanding of GMP standards and quality documentation practices

+ Experience assisting with audits, investigations, and corrective action processes

+ Strong attention to detail with solid organizational, analytical, and communication skills

+ Background in cosmetics, dietary supplements, pharmaceuticals, food manufacturing, or related industries preferred

+ Familiarity with regulatory frameworks such as ISO 22716, 21 CFR Part 111, or MoCRA is a plus

+ Bachelor's degree in Chemistry, Biology, Food Science, or a related field preferred (equivalent experience considered)

** Position Details*
* + Full-time, on-site position in Chattanooga, TN

+ Day shift schedule, Monday through Friday

+ Opportunity for growth within a growing manufacturing environment

** About the Role*
* A Chattanooga-based manufacturer specializing in personal care products, cosmetics, and nutritional supplements is seeking a  
** Quality Assurance & Quality Control Specialist
** to join its on-site operations. This organization supports both established and emerging brands through integrated product development, manufacturing, and quality systems.

** Position Overview*
* This full-time, on-site role focuses on supporting quality activities across regulated manufacturing operations. The specialist will play a key role in maintaining compliance, overseeing production quality, managing documentation, and contributing to continuous improvement efforts.

Working cross-functionally with production, R&D, and leadership teams, this individual will help identify risks, resolve quality concerns, and ensure adherence to internal standards and regulatory requirements.

** Key Responsibilities*
* + Assist with daily QA/QC processes within manufacturing operations

+ Review batch records, production documentation, and quality data for accuracy and compliance

+ Perform inspections of raw materials, packaging components, and finished goods

+ Monitor production and packaging activities to ensure quality standards are met

+ Maintain and update quality systems, documentation, and procedures

+ Support investigations, corrective actions, and audit readiness

+ Coordinate product testing with third-party laboratories

+ Communicate quality issues and contribute to timely resolution efforts

** Qualifications*
* + Minimum of 2 years of experience in a QA/QC role within a regulated manufacturing environment

+ Understanding of GMP standards and quality documentation practices

+ Experience assisting with audits, investigations, and corrective action processes

+ Strong attention to detail with solid…
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