What are the responsibilities and job description for the Manufacturing & Quality Compliance Consultant position at United Consulting Hub?
We are seeking an experienced Manufacturing & Quality Compliance Consultant to support pharmaceutical and biotechnology manufacturing operations on a contract basis.
🔹 Key Responsibilities:
• Deviation investigation and management
• Change Control authoring, review, and execution
• Batch Record Review and GMP documentation support
• Protocol development and review (Validation, Qualification, and Laboratory Protocols)
• Manufacturing floor support and technical troubleshooting
• Quality investigations, root cause analysis, and CAPA implementation
• Laboratory documentation and compliance support
• Technical and Quality Oversight for GMP manufacturing operations
• Cross-functional collaboration with Manufacturing, Quality, Validation, and Laboratory teams
🔹 Qualifications:
• Strong experience in GMP-regulated pharmaceutical, biotechnology, or medical device environments
• Hands-on experience with deviations, investigations, change controls, and batch record review
• Knowledge of FDA regulations, cGMP requirements, and quality systems
• Excellent technical writing, problem-solving, and communication skills