More jobs:
QA/QC Specialist
Job in
Chattanooga, Hamilton County, Tennessee, 37404, USA
Listed on 2026-06-08
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
* 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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