Sr. Packaging & Labelling Engineer

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.

We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

Senior Packaging and Labeling Engineer to lead the development, validation, and execution of packaging and labeling solutions for our products. This role involves working with vendors to build and validate packaging machines, ensuring compliance with regulatory requirements, and optimizing packaging processes to improve efficiency and sustainability. The ideal candidate will bring expertise in packaging design, material selection, labeling systems, and packaging machinery validation, particularly in industries such as medical devices and pharmaceuticals.

Manage related equipment and process validations as required under the Quality system change control process. Coordinate the integration of new products and processes into the manufacturing systems and processes.

• Design, develop, and optimize packaging systems (pouches, blister trays, cartons, labels, boxes, shrink wraps, etc.) to meet functional, quality, and regulatory requirements.
• Conduct material evaluation, testing, and selection with consideration for compatibility, sustainability, manufacturability, durability, and cost.
• Lead or support root‑cause investigations and implement improvements for packaging-related performance issues.

• Lead or contribute to prototype design, assembly, testing, and line trials to validate new packaging concepts.
• Develop and refine packaging manufacturing processes, including equipment specification, qualification, and validation.
• Collaborate closely with Engineering, Operations, Quality, Regulatory, and Supply Chain to ensure smooth technology transfer to production.

• Oversee installation, commissioning, operation, and maintenance readiness of packaging machinery and inspection systems (e.g., vision systems, inline verification).
• Troubleshoot equipment or system performance and drive corrective and preventive actions to maintain efficiency and quality.

• Integrate quality assurance and control requirements into packaging and process design.
• Ensure adherence to technical standards, regulatory guidelines, and global packaging/labelling regulations.
• Perform or support risk assessments (pFMEA, QRA) for packaging components and processes.
• Follow GxP, SOPs, and documentation requirements to ensure full traceability and audit readiness.

• Create, review, and manage product artwork within the Artwork Management System.
• Ensure labelling accuracy and regulatory compliance across all markets.
• Support change control processes related to artwork, packaging, and labelling updates.

• Identify and implement improvements in packaging robustness, sustainability, cost, and manufacturability.
• Make informed technical decisions within your area and contribute to broader project and organizational objectives.

• Bachelor’s degree or higher in Packaging Engineering, Mechanical Engineering, Materials Science, Industrial Engineering, or related technical field.
• 5+ years of experience in packaging engineering, ideally within medical device, pharmaceutical, or other regulated manufacturing environments.
• Strong understanding of packaging materials (plastics, films, foils, paperboard, adhesives) and their performance characteristics.
• Hands‑on experience with packaging equipment, automation systems, and vision/inspection systems (preferred).
• Working knowledge of equipment qualification and process validation (IQ/OQ/PQ), as well as design controls.
• Experience with CAD tools and engineering documentation (drawings, specifications, BOMs).
• Familiarity with Artwork Management Systems and labelling compliance requirements.
• Knowledge of GxP, ISO 11607, FDA 21 CFR Part 820, EU MDR, and other relevant regulatory frameworks.
• Ability to perform risk assessments (FMEA, QRA) and apply quality control methodologies.
• Proficiency with statistical tools (e.g., Minitab) is a plus. Excellent communication skills, with the ability to explain technical concepts to diverse stakeholders.
• Detail‑oriented, proactive, and committed to high standards of quality and compliance.

• Opportunity to work with a leading global medical device company.
• Collaborate with a diverse and talented team in a supportive work environment.
• Competitive compensation package and comprehensive benefits.
• Continuous learning and development opportunities.