Description

You will support quality operations within a pharmaceutical manufacturing environment.

Responsibilities

• Maintain quality management systems to ensure compliance with industry standards.
• Execute quality control and quality assurance protocols during production cycles.
• Manage technical documentation and records within the document management system.
• Monitor adherence to GMP guidelines across all operational processes.

Required Skills

• 5+ years of experience in quality-related roles.
• Deep understanding of GMP (Good Manufacturing Practice) requirements.
• Practical experience with Quality Management Systems (QMS).
• Proficiency in Quality Control (QC) and Quality Assurance (QA) methodologies.
• Strong competency in Document Management processes.
• Bachelor's degree or equivalent graduate-level education.

Preferred Skills

• Ability to work onsite in Elkton, VA.

Key Skills

Education

ANY GRADUATE