Technician I, Sterile Production Operations

Alcon Research•Fort Worth, AS

1d•Onsite

About The Position

This role is part of Alcon's Manufacturing function, a team that designs, produces and delivers innovative eyecare products to more than 140 countries through operational excellence and efficiency. The Technician I, Sterile Production Operations (Science/Tech/Engineering Path), is primarily responsible for performing technical tasks related to processing ingredients and pharmaceutical products. You will operate manufacturing equipment, handle raw materials and finished products, and perform general maintenance, all while ensuring compliance with procedures and maintaining product quality. Specifics include: Perform technical tasks related to processing ingredients and pharmaceutical products, ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements. Operate manufacturing equipment such as autoclaves, ovens, stills, filtration apparatus, and sterile filling equipment. Handle raw materials and finished products. Perform general maintenance. Follow standard operating procedures, maintain records, and participate in quality checks. Inspect products, address deviations and issues promptly, and maintain accurate and complete documentation to ensure compliance with GMP requirements and rigorous quality control. Complete all required training and contribute to the overall compliance of the organization, committing to continuous improvement and adherence to regulatory requirements. All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.

Requirements

High School Diploma or equivalent
The ability to fluently read, write, understand and communicate in English

Responsibilities

Perform technical tasks related to processing ingredients and pharmaceutical products, ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
Operate manufacturing equipment such as autoclaves, ovens, stills, filtration apparatus, and sterile filling equipment.
Handle raw materials and finished products.
Perform general maintenance.
Follow standard operating procedures, maintain records, and participate in quality checks.
Inspect products, address deviations and issues promptly, and maintain accurate and complete documentation to ensure compliance with GMP requirements and rigorous quality control.
Complete all required training and contribute to the overall compliance of the organization, committing to continuous improvement and adherence to regulatory requirements.
Adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training.
Meet individual job requirements and contribute to the overall compliance of the organization.