Technician I, Sterile Production Operations (B Shift)

Alcon Research•Fort Worth, AS

41d•Onsite

About The Position

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us? As a Technician I, Sterile Production Operations, you will be trusted to work on performing technical tasks related to processing ingredients and pharmaceutical products at our Manufacturing Facility in Fort Worth ASPEX, TX! In this role, a typical day will 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 thorough quality control. Complete all required training and contribute to the overall compliance of the organization, committing to continuous improvement and adherence to regulatory requirements.

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 thorough quality control.
Complete all required training and contribute to the overall compliance of the organization, committing to continuous improvement and adherence to regulatory requirements.