Operator I, Sterile Production Operations (S)

Alcon•Fort Worth, TX

8d•Onsite

About The Position

The Operator I, Sterile Production Operations role is part of Alcon's Manufacturing function, which designs, produces, and delivers eyecare products to more than 140 countries. The position is primarily responsible for complex production tasks involving the processing of ingredients and pharmaceutical products. It operates and maintains manufacturing equipment, handles raw materials and finished products, and performs general maintenance. The role requires technical skills, attention to detail, problem-solving abilities, and adherence to procedures. The position is onsite in Fort Worth, Texas, with a Monday–Friday schedule from 2:30 p.m. to 11:00 p.m. Travel requirements are 0–10%. Relocation assistance and sponsorship are not available. Associates must follow GxP regulations and standard operating procedures, maintain accurate and complete documentation, ensure rigorous quality control, and complete required training. Alcon describes opportunities for career growth and development and offers a benefits package that includes health, life, and retirement benefits, flexible time off for exempt associates, and PTO for hourly associates.

Requirements

High school diploma or equivalent.
Ability to fluently read, write, understand, and communicate in English.

Responsibilities

Manage complex production tasks related to processing ingredients and pharmaceutical products while complying with GMP and regulatory requirements.
Operate and maintain manufacturing equipment, including autoclaves, ovens, stills, filtration apparatus, and sterile filling equipment.
Handle raw materials and finished products.
Perform general maintenance.
Inspect products, follow standard operating procedures, maintain accurate documentation, and promptly address deviations and issues.
Participate in quality checks and process improvement initiatives.
Complete required training and meet individual job requirements to contribute to organizational compliance.
Follow GxP regulations and commit to continuous improvement and regulatory compliance.