Quality Control Tech

Job Description

This position is responsible for efficient and effective performance of sampling raw materials and testing (except for the raw materials chemicals) in conformance with regulations and standards.

• Maintain Quality Reports.
• Maintain and implement efforts in housekeeping and safety programs.
• Maintain the cleanliness and orderliness of Metrology Laboratory.
• Perform raw material sampling.
• Perform raw material inspections (Except for the raw materials chemicals).
• Understands and consistently follows multi-step documented procedures while conducting Inspections.
• Maintains accurate and well-organized Inspection records, notebooks and/or worksheets.
• Maintenance of the Calibration and Preventive Maintenance programs for equipment.
• Provide QC support for new product development/Launch/Capacity Expansion projects.
• Support any Waste Reduction Initiatives that involve Incoming Inspection.
• Demonstrate Regulatory Compliance such as FDA inspection readiness, Corporate Audits, Internal Audits and maintain Training Compliance.
• Demonstrate Safety Compliance such as Strive for Zero Serious Accidents in the plant.
• Contribute for the overall Safety Index plant goal of >98%.
• Must have awareness and respect of all company policies and safety rules.
• Maintain appropriate training/certification including GLP and GMP.

• High School diploma.
• Experience in Quality Control, Incoming Inspection, or Metrology Laboratory operations preferred.
• Strong understanding of GLP, GMP, and regulatory compliance requirements.
• Ability to follow detailed, multi-step procedures with a high level of accuracy and attention to detail.
• Experience maintaining calibration and preventive maintenance records for laboratory or inspection equipment.
• Strong organizational, documentation, and communication skills.
• Demonstrated commitment to safety, quality, and continuous improvement.
• 1-2 years' experience reading drawings and using measuring tools like caliper, ruler and vision system, preferred.
• Conversant with GLP/GCP/cGMP and global Drug and Device Development Processes, preferred.