Technician I, Sterile Production Operations

• 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
 

• Minimum NITEC in Engineering field with 1 year of relevant experience in a manufacturing environment, preferably in cGMP

• Familiarity with aseptic techniques and cleanroom practices.

• Ability to work independently with minimal supervision.

• Team player Proficient in basic computer applications (e.g., Microsoft Office, production systems).

• High attention to detail with a commitment to quality.

• Comfortable working in a controlled cleanroom environment with strict gowning requirements.

• Knowledge of health, safety, and environmental (HSE) responsibilities in a manufacturing setting.

• Able to work 8 hours rotating shift.

• Able to carry loads up to 25kg

At Alcon, we are committed to fostering a work environment where our employees can grow, innovate, and excel. Here’s how you can thrive in your role with us:

See your impact at alcon.com/careers

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Ability to work on shift

• Ability to carry loads of up to 25kg

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