Sr. Manufacturing Engineer

Key Responsibilities:

• Adhere to product Safety and Quality guidelines.
• Monitor and implement quality procedures for manufacturing, packing, inspecting, and handling products.
• Adjust production programs within set time-lines, ensuring variations stay within acceptable limits.
• Maintain accurate documentation for production programs and investigate repetitive causes of product defects.
• Track indicators of quality, productivity, scrap, and validate protocols for products, processes, machinery, and equipment.
• Verify the operation and calibration of equipment and controls in clean-room environments before, during, and after transfers.
• Provide support for additional tasks as needed by the company.

• Minimum of 3 years in medical product manufacturing industry preferred.
• Proficient in handling product and process documentation in accordance with FDA and ISO procedures and work instructions.
• Knowledge on integrating new products and processes.
• Expertise in validation protocols and product/equipment validation.
• Advanced knowledge of statistical controls.

Medical devices manufacturing company located in Tijuana, Baja California, Mexico.

Competitive compensations package