United Consulting Hub is seeking a motivated Quality Systems Associate to support quality operations, compliance activities, and continuous improvement initiatives within a regulated pharmaceutical or life sciences environment. This role is well suited for recent graduates interested in Quality Assurance, regulatory compliance, and validation processes.
Responsibilities:
- Assist in maintaining and improving Quality Management Systems (QMS)
- Support compliance with GMP regulations, internal procedures, and quality standards
- Participate in deviation investigations, root cause analysis, and documentation activities
- Support CAPA (Corrective and Preventive Action) tracking and follow-up
- Review quality records, batch documentation, and related reports for completeness and accuracy
- Assist with preparation and coordination of internal and external audits
- Collaborate with manufacturing, Quality Control (QC), and R&D teams on quality-related initiatives
- Support validation and qualification documentation activities
- Maintain documentation in accordance with Good Documentation Practices (GDP)
- Monitor and report quality metrics including deviations, complaints, and corrective actions
Requirements:
- Basic understanding of Quality Management Systems and quality processes
- Familiarity with GMP regulations and compliance standards
- Knowledge of deviation management, CAPA, and change control concepts
- Strong analytical, organizational, and problem-solving abilities
- Effective written and verbal communication skills
- Proficiency in Microsoft Office applications, especially Excel and Word