QMS Associate: Audit Ready, CAPA & Documentation

Meissner; Athens (GA); Presencial; USD 68.000 - 87.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Full Medical, Dental and Vision with H

HSA Employer Contributions

HQ Onsite Gym

Coffee bars

Free EV charging

Employee discounts

401k and Profit Sharing

Company Sponsored Life Insurance

Employee Assistance Program

Paid Time Off & Holidays

Descripción de la vacante

Meissner is seeking an Associate Quality Management Systems Specialist in Athens, GA. The role focuses on maintaining and improving the Quality Management System to ensure cGMP compliance and client requirements.

You will support document control, CAPA, deviations, and audit readiness while collaborating with Commercial and Technical Operations teams. The position emphasizes attention to detail and cross-functional communication in a fast-paced pharma environment.

Formación

• 2+ years of experience in a Quality Assurance role within pharma/biotech.
• Bachelor’s degree in a scientific/engineering discipline preferred.
• Working knowledge of cGMP regulations and quality systems (CAPA, deviations, OOS, document control).
• Experience with electronic Quality Management Systems (eQMS) or document management systems preferred.
• Strong attention to detail with ability to review GMP documentation for accuracy and compliance.
• Ability to manage multiple priorities in a fast-paced, regulated environment.
• Excellent written and verbal communication, cross-functional collaboration.

Responsabilidades

• Maintain and improve the Quality Management System to ensure cGMP compliance.
• Provide QA SME support across document control, CAPA, deviations and audits.
• Track metrics, perform system administration, and support continuous improvement.
• Assist with internal and external audits and readiness activities.
• Oversee document control processes and electronic documentation system usage.
• Ensure regulatory documentation and SOPs meet requirements.
• Review testing and log documentation for compliance and traceability.

Conocimientos

Quality Assurance

cGMP knowledge

Document control

CAPA

Deviations

Audit readiness

Interdepartmental comms

Educación

Bachelor's degree in science or engineering

Herramientas

eQMS

Document management system

Descripción del empleo

Meissner is seeking an Associate Quality Management Systems Specialist in Athens, GA. The role focuses on maintaining and improving the Quality Management System to ensure cGMP compliance and client requirements.

You will support document control, CAPA, deviations, and audit readiness while collaborating with Commercial and Technical Operations teams. The position emphasizes attention to detail and cross-functional communication in a fast-paced pharma environment.