Katalyst Healthcares and Life Sciences is looking for Quality Control Tech 1 in El Paso, TX. This local job opportunity with ID 3662830703 is live since 2026-05-04 14:28:34.

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.
Responsibilities:

• 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.
• udits and maintain Training Compliance.
• Demonstrate Safety Compliance such as Strive for Zero Serious Accidents in the plant.
• Contribute for a successful EH&S Audits with 0 major observations and 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.

Requirement:

• High School diploma.
• Experience in Quality Control, Incoming Inspection, or Metrology Laboratory operations preferred.
• Strong understanding of GLP, GMP, and regulatory compliance requirements.
• bility 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.