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.
Operational Areas:
The successful candidates will be placed in one of the following areas based on the outcome of the interview:
- Compounding – Preparation of ophthalmic products and maintaining cleanroom/equipment conditions
- Filling – Aseptic filling of ophthalmic products in sterile environments
- Packaging – Packaging of ophthalmic products according to cGMP standards
- Repair & Maintenance – Maintenance, troubleshooting, and repair of manufacturing equipment
Detailed job descriptions for each area are included in the attachment/section below.
1. Compounding
- Prepare, operate and monitor all equipment associated with the compounding of ophthalmic products in accordance with current Good Manufacturing Practices (cGMP).
- Perform routine cleaning and sanitization on all equipment and rooms associated with compounding processes.
- Prepare, verify and transfer materials/components used in Compounding.
- Execute activities in support of validations associated with Compounding.
- Perform and review all necessary documentation as required and in accordance with Good Documentation Practice (GDP).
- Prepare, operate and monitor all equipment associated with the compounding of ophthalmic products in accordance with current Good Manufacturing Practices (cGMP).
- Perform routine cleaning and sanitization on all equipment and rooms associated with compounding processes.
- Assist in the investigation of process deviations and work in a team to identify and work on opportunities for productivity/process improvements.
2.Filling
- Prepare, operate and monitor all equipment associated with the filling of ophthalmic products, in accordance with the current Good Manufacturing Practices (cGMP).
- Perform routine cleaning and sanitization on all equipment and rooms associated with aseptic filling, and steam sterilization of the necessary production/cleaning equipment/components, including the operation and routine cleaning of steam sterilizer.
- Perform routine microbiological sampling for environmental and personnel monitoring in a clean room environment.
- Prepare, verify and transfer materials/components used in aseptic filling. Execute activities in support of validations associated with cleaning and aseptic filling.
- Perform all filling functions/responsibilities including MBR reviews and JDE/SAP transactions.
- Assist in the investigation of process deviations and work in a team to identify and work on opportunities for productivity/process improvements.
3.Packaging
- Prepare, operate and monitor all equipment associated with the packaging of ophthalmic products, in accordance to current Good Manufacturing Practices (cGMP).
- Perform line set up, line start-up, housekeeping and associated activities, in process sampling and inspection.
- Perform routine cleaning on all equipment associated with packaging.
- Perform transfer of materials/ components used in packaging.
- Perform activities in support of validations associated with packaging.
- Perform and review all necessary documents as required and in accordance to Good Documentation Practice (GDP).
- Assist in the investigation of process deviation and work in a team to identify and work on opportunities for productivity/process improvements.
4.Repair & Maintenance
- Perform maintenance work in accordance to approved SOPs and job plans generated from the preventative and corrective maintenance management system.
- Ensure that all PM plans are executed without any overdue maintenance.
- Support trouble-shooting and repair activities for critical equipment (CM) while minimizing Production downtime to support reliable manufacturing operations.
- Support daily production activities (e.g. equipment format change) to get desired production output and meet product quality.
- Strict adherence to cGMP and GDP (SOPs, PMs, CMs, etc.). Reporting any discrepancies in a timely manner.
- Ability to work and share additional tasks and responsibilities (PM, CM, Production Overtime, etc.) as necessary. The role will also require a rotating three-shift pattern.
- Strict adherence to all site safety requirements and focus on opportunities for improvement.
- Oversee and responsibility for contractors / vendors on site in the execution of their duties to ensure maintenance services or equipment improvement.
- Support short term problem solving and short / long term continuous improvement or manufacturing equipment (Compound, Fill & Pack) to assure product quality, productivity and process enhancement.
- Shift reporting of all daily duties both in written and verbal communications.
- Ensure medium and low risk level controlled supply item (CSI) incoming inspection, review of Material certificates/ COCs/COAs and the use at GMP environment upon SQA approval.
- Utilization of Alcon Senior Mechanics, Engineering, Leads, Engineering management in addition to vendors to developing electrical, mechanical, trouble shooting and process knowledge for the Compound, Filling and Packaging area (e.g. schematic drawings & vendor manuals).
WHAT YOU’LL BRING TO ALCON:
- No experience required or with minimum NITEC in Engineering field with 1 year of relevant experience in a manufacturing environment, preferably in the pharmaceutical or healthcare industry.
- Strong technical and mechanical aptitude.
- Familiarity with aseptic techniques and cleanroom practices.
- Ability to work independently with minimal supervision.
- Team player with effective communication and interpersonal skills.
- Proficient in basic computer applications (e.g., Microsoft Office, production systems).
- High attention to detail with a commitment to quality.
- Self-motivated, proactive, and willing to learn and adapt.
- Comfortable working in a controlled cleanroom environment with strict gowning requirements.
- Knowledge of health, safety, and environmental (HSE) responsibilities in a manufacturing setting.
- Open to 8-hour weekday rotating shifts (12-hour 24/7 shift may apply later)
HOW YOU CAN THRIVE AT ALCON:
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:
- Career Growth & Development – Gain access to continuous learning opportunities, leadership training, and career advancement programs to support your professional journey.
- Collaborative Culture – Work alongside passionate and diverse teams in a dynamic and inclusive environment that encourages innovation and teamwork.
- Impactful Work – Be part of a purpose-driven company that is improving lives by advancing eye care solutions worldwide.
- Recognition & Rewards – Your contributions are valued and recognized through competitive compensation, performance incentives and career progression opportunities.
- Global Exposure – Join a world-class organization with opportunities to collaborate across international teams and gain global industry insights.
- Work-Life Balance & Well-Being – Enjoy employee wellness programs, flexible work arrangements and initiatives that support your well-being.
At Alcon, we empower our people to make a difference while growing their careers in an exciting and supportive environment. Join us and see brilliance in every opportunity!
ALCON Careers
See your impact at alcon.com/careers
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You are applying to be part of the Alcon Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV or resume.
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