COMPANY OVERVIEW: At Alcon, we are inspired by the meaningful work we do to help people see brilliantly. As the global leader in eye care, we boldly innovate, champion progress, and act with speed. We recognize and celebrate the contributions of our people, offering career opportunities that empower growth and fulfillment. Together, we go above and beyond to make a lasting impact on the lives of our patients and customers. We cultivate an inclusive culture and invite diverse, talented individuals to join us in shaping the future of eye care.
Role Overview: As a Technician I in Sterilize Productions Operations, you will play a vital role in preparing ophthalmic products, ensuring all activities comply with current Good Manufacturing Practices (cGMP) and safety standards. You will work closely with the Supervisor and team members, operating equipment, performing sanitization, and maintaining a cleanroom environment to meet quality and efficiency standards.
Key Responsibilities:
- Operate, monitor, and maintain equipment used in the compounding of ophthalmic products according to cGMP requirements.
- Prepare and verify materials and components for compounding processes.
- Perform cleaning and sanitization of equipment, tools, and rooms to maintain aseptic conditions.
- Support validation activities, including equipment and process validation relevant to compounding.
- Ensure proper documentation practices (cGMP) are followed for all production and cleaning records.
- Assist in investigating deviations, identifying root causes, and implementing corrective actions.
- Participate in continuous improvement initiatives to enhance productivity, efficiency, and quality.
- Identify and escalate safety concerns; stop unsafe practices.
- Conduct daily 5S housekeeping activities to ensure a clean and organized work environment.
- Maintain site readiness for audits and inspections by adhering to SOPs, cGMP, and safety protocols.
- Provide guidance and on-the-job training to junior operators.
- Participate in risk assessments for new processes and equipment.
- Drive initiatives to reduce waste, control costs, and improve equipment effectiveness (OEE).
- Manage production activities to ensure timely delivery of high-quality products.
Qualifications:
- Minimum NITEC in Engineering or related field with 1 year of relevant experience in manufacturing, preferably in pharmaceutical or healthcare industry.
- Strong technical and mechanical aptitude.
- Knowledge of aseptic techniques and cleanroom practices.
- Ability to work independently with minimal supervision.
- Effective communication and interpersonal skills.
- Proficient in basic computer applications (e.g., Microsoft Office, production systems).
- High attention to detail and commitment to quality.
- Self-motivated, proactive, adaptable, and willing to learn.
- Comfortable working in a controlled cleanroom environment with gowning requirements.
- Knowledge of health, safety, and environmental (HSE) responsibilities.
- Able to work 12-hour rotating shifts.
Growth Opportunities:
- Career development through continuous learning, leadership training, and advancement programs.
- Collaborate with diverse, passionate teams in an inclusive environment.
- Contribute to impactful work improving lives worldwide.
- Recognition through competitive compensation and performance incentives.
- Global exposure with opportunities for international collaboration.
- Supportive initiatives for work-life balance and well-being.
Join Alcon and see brilliance in every opportunity! For more details, visit alcon.com/careers.