QC Analyst

QC Analyst

Requirements

• Minimum 3 years of lab experience in cGMP quality control or production environment
• Must have cGMP experience in a quality function supporting manufacturing operations
• Familiarity with basic laboratory equipment (balances, moisture analyzers, pH meters) a plus.

Responsibilities

• Assist with support duties such as filling product, labeling product, testing samples, and taking inventory
• Write control documents like Standard Operating Procedures (SOPs), product disposition, and facilitating or participating in quality system failures investigations. Maintain cGMP principles and Good Documentation Practices.
• In-process testing, sample prep, documentation, and maintaining sample inventory
• GC(Gas Chromatography): Sample Prep/Light Preventative Maintenance/Running GC
• Participate in internal and external audits, ensuring compliance with regulatory requirements such as FDA, ISO, and cGMP guidelines.
• Collaborate with Research & Development (R&D) and Production teams to ensure smooth product launches and continuous quality improvements.
• Maintain and calibrate laboratory equipment to ensure precision in testing.
• Help prepare experiments and projects as needed
• Maintain records and data as needed
• Work closely with the lab staff to work on special projects as needed
• Follow guidelines and comply with all company safety, quality, and training procedures and regulations
• Perform additional duties as assigned

Preferred Qualifications

• BS in a Science related field preferred
• Gas Chromatography experience preferred, will train the right candidate