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Quality Associate 1

Thorne

Job Location:

Summerville, SC - USA

Monthly Salary: Not provided by the employer

Posted: 11 July 2026 (30+ days ago)

Application Deadline: 8 October 2026

Vacancies: 1 Vacancy

Job Summary

At Thorne we work to deliver high-quality science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. At Thorne youll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage.

The Quality Associate I supports Thornes Quality Management System (QMS) by assisting with quality processes documentation and compliance activities that help ensure products consistently meet company customer and regulatory requirements. This role provides operational support for key quality systems including product certifications Change Control Corrective and Preventive Actions (CAPA) deviations customer complaints nonconforming materials and document control.

Working closely with Quality Operations Regulatory Affairs Product Development and Supply Chain the Quality Associate I develops a strong foundation in quality systems while contributing to continuous improvement initiatives and daily quality operations. The ideal candidate is detail-oriented highly organized and eager to learn within a regulated manufacturing environment while building expertise in GMP requirements and quality management processes.

RESPONSIBILITIES

Support the administration of Thornes Quality Management System (QMS) including Change Control Corrective and Preventive Actions (CAPA) Deviations Nonconforming Materials (NCM) customer complaints and document control activities.
Assist in coordinating third-party product certification activities by gathering documentation and communicating with certification bodies contract manufacturers and internal stakeholders.
Support the stability program by coordinating sample submissions maintaining documentation and assisting with stability data collection and reporting.
Assist with customer complaint investigations by collecting information documenting findings and supporting timely resolution.
Maintain organize and update quality documentation including Standard Operating Procedures (SOPs) controlled forms and quality records.
Participate in internal audits and inspections while supporting audit preparation and follow-up activities.
Assist in reviewing new products processes and documentation to help ensure compliance with GMP requirements and internal quality standards.
Generate routine quality reports KPI metrics and status updates to support quality system monitoring.
Complete ERP and ETQ transactions related to quality processes and maintain accurate electronic records.
Collaborate with cross-functional teams to support quality initiatives and continuous improvement efforts.
Maintain compliance with GMP FDA OSHA and all applicable company policies and regulatory requirements.
Escalate quality concerns or potential compliance issues to appropriate team members and support timely resolution.
Perform other duties as assigned.

WHAT YOU NEED

Education & Experience

High school diploma or GED required; Associates or Bachelors degree in a scientific discipline Quality Manufacturing or a related field preferred.
02 years of experience in Quality Assurance Manufacturing Laboratory Operations Regulatory Affairs or a related field preferred.
Internship co-op or experience within a GMP-regulated manufacturing environment is a plus.
Familiarity with quality management systems or regulated manufacturing environments is preferred.

Technical Knowledge

Basic understanding of Good Manufacturing Practices (GMP) and quality system principles.
Ability to interpret Standard Operating Procedures (SOPs) work instructions and technical documentation.
Proficiency with Microsoft Office Suite and willingness to learn ERP and electronic Quality Management Systems (eQMS) such as ETQ.
Ability to prepare accurate documentation reports and quality records.

Core Competencies

Strong attention to detail and commitment to accuracy.
Excellent organizational and time management skills with the ability to prioritize multiple assignments.
Strong verbal and written communication skills.
Ability to work collaboratively in a cross-functional team environment while developing independent decision-making skills.
Demonstrated initiative curiosity and a willingness to learn new quality systems and regulatory requirements.
Analytical problem-solving skills with the ability to recognize and escalate quality concerns appropriately.
Adaptability and a commitment to continuous improvement in a fast-paced manufacturing environment.

WHAT WE OFFER