QC Lab Technician

Description

Since 1946, The Jet Pulverizer Company, Inc. has been committed to providing state-of-the-art processing equipment and services. The continuous technological advancement of our line of Micron-Master® Jet Pulverizers and ongoing modernization and expansion of our Custom Grinding Division provide our customers with unsurpassed value and quality in both jet pulverizing equipment and custom grinding services. The Quality Technician plays a crucial role in ensuring the safety, quality, and compliance of products manufactured within our FDA-regulated micronization facility.

This position involves monitoring production processes, conducting inspections, and collaborating with cross-functional teams to maintain high standards.

Essential Duties of the QC Lac Tech:

PRIORITY - Product sample testing as required

• Complete paperwork on a timely basis
• Create sample composites and retains as indicated by customer need
• Generate CoA’s as required
• Stock sample cups and lids
• Monitor lab consumables and order as needed
• Maintain clean lab
• Monitor calibration status of instrumentation and calibrate as required
• Perform routine inspections of raw materials, intermediate products, and finished goods.
• Utilize precision measuring instruments and testing equipment to verify product specifications.
• Identify any deviations from quality standards and report findings promptly.
• Monitor micronization processes, including particle size reduction, blending, and packaging.
• Collect samples at various stages of production for analysis.
• Ensure adherence to standard operating procedures (SOPs) and regulatory guidelines.
• Maintain accurate records of inspections, test results, and corrective actions.
• Prepare quality reports and communicate findings to supervisors and management.
• Collaborate with the Quality Assurance team to address non-conformities.
• Assist during internal and external audits, including FDA inspections.
• Ensure compliance with cGMP (current Good Manufacturing Practices) and other relevant regulations.
• Support the implementation of quality management systems.
• Provide guidance on quality-related matters to colleagues.
• Foster a culture of quality awareness and accountability.
• Must be willing to work overtime as needed, including some mandatory weekend shifts.

• HS Diploma required. Associate degree preferred.
• Computer proficiency – Microsoft Windows/Outlook, Microsoft Office
• 1 – 2 years lab experience
• Experience working in an FDA-regulated environment (pharmaceuticals, medical devices, or related industries).
• Proficiency in using measurement tools (calipers, micrometers, etc.) and analytical instruments.
• Knowledge of cGMP, ISO standards, and quality control principles.
• Strong attention to detail, problem-solving skills, and ability to work independently.
• Excellent communication and teamwork abilities.