GMP QA Associate: Growth, Training & Impact

Union-Agener; Augusta (GA); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

Benefits Package

Job summary

Union-Agener in Augusta, GA is seeking a Quality Assurance professional to oversee systems and functional areas, prepare and review GMP documents, implement and maintain records for cGMP compliance, and support regulatory inspections.

The role requires a BS in a science field, manufacturing QA/QC experience in FDA-regulated facilities, strong communication, teamwork, and the ability to provide hands-on support in a 24/7 plant environment with on-call duties.

Qualifications

• Bachelor of Science Degree (4 year college).
• Experience in Quality Assurance, Quality Control, Engineering, Operations, Technology in FDA-regulated manufacturing with cGMP.
• Excellent verbal and written communication tailored to audience.
• Ability to work well across all levels in a manufacturing environment.
• Strong planning, organization, and prioritization skills.
• Team-building and facilitation of action plans.
• Proficiency with Microsoft Office applications.

Responsibilities

• Oversee specific systems or functional areas as assigned.
• Prepare, review, redline, and/or approve GMP documents supporting the site.
• Implement and maintain systems for documentation and control of records for cGMP compliance.
• Evaluate quality impact of GMP incidents and support long-term resolutions.
• Participate in inspections and educate site personnel on quality matters.
• Back-up for other QA colleagues and track/report issues.
• Perform Change Control, documentation, and drawing requests.

Skills

Project management

Results oriented

Interpersonal skills

Communication

Organizational skills

Adaptability

On-call support

Education

Bachelor of Science

Tools

Microsoft Office

SAP

SE Suite

Job description

Union-Agener in Augusta, GA is seeking a Quality Assurance professional to oversee systems and functional areas, prepare and review GMP documents, implement and maintain records for cGMP compliance, and support regulatory inspections.

The role requires a BS in a science field, manufacturing QA/QC experience in FDA-regulated facilities, strong communication, teamwork, and the ability to provide hands-on support in a 24/7 plant environment with on-call duties.