About Event
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 – Prepare ophthalmic products in cleanroom environments under strict GMP standards
- Filling – Perform aseptic filling operations in sterile conditions
- Packaging – Pack products in compliance with cGMP requirements
- Repair & Maintenance – Troubleshoot and maintain equipment to support manufacturing operations
- Molding & Tooling Ops – Operate and troubleshoot molding tools, perform lens inspections, mold changeovers, and precision measurements in a GMP-compliant environment
- DSM Flex Production – Operate automated equipment to produce, package and sterilize contact lenses, ensuring high-quality standards
- Light Stream (LS1) Production - Manages complex equipment setup, operation, maintenance, troubleshooting, and quality monitoring in production.
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).
5. Molding & Tooling Ops
- Operating molding tools and automated equipment with minimal supervision.
- Conducting quality inspections using gauges and fixtures and performing statistical monitoring to ensure compliance with standards.
- Handling materials and performing mold changes and changeovers
- Collaborating with cross-functional teams for mold troubleshooting and maintenance.
- Conducting optical tool inspection, mechanical checks, line clearance, set-up, and lens inspection.
- Following work instructions and adhering strictly to GMP/GDP and GxP requirements.
- Resolving production issues as they arise and maintaining accurate documentation.
- Actively participating in continuous improvement initiatives to enhance efficiency and product quality.
- Completing all required training and ensuring full regulatory compliance in all activities.
6. DSM Flex Production
- Operate the DSM Flex line collaboratively with the team to manufacture high-quality products.
- Operate autoclave machines for the sterilization of contact lenses.
- Perform lot changes and routine maintenance on DSM Flex lines.
- Maintain excellent 5S standards and ensure batch documentation is complete and compliant with procedures for DSM Flex lines and related equipment, including autoclaves.
- Proactively initiate and implement at least one Kaizen improvement idea annually.
7. Light Stream (LS1) Production
- Handle complex technical tasks to support operations and improve efficiency within established procedures.
- Set up, operate, maintain, and troubleshoot production equipment.
- Manage resources and schedules to meet specifications, production volume, cost, wastage targets, and quality standards.
- Move, pack, and sort raw materials or finished goods as needed.
- Monitor output quality to identify, reject, or rework faulty products.
- Maintain accurate daily production records for performance analysis.
- Make minor operational decisions requiring technical expertise and problem-solving skills.
- Review work orders, schedule resources, and oversee manufacturing operations to align with business goals and drive operational excellence.
- Adhere to GxP regulations by following SOPs, maintaining accurate documentation, ensuring quality control, and completing mandatory training.
- Commit to regulatory compliance and continuous process improvement.
WHAT YOU’LL BRING TO ALCON:
- No prior experience required or with a minimum NITEC qualification in Engineering (e.g., Pharmaceutical Science, Chemical Engineering, Mechanical Engineering, or Electrical Engineering) and at least 1 year of relevant experience in a manufacturing environment, preferably within the pharmaceutical or healthcare industry, will be an advantage.
- 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.
- Able to work 12 hours rotating shift.