Molding Engineer II, Molding & Tooling Engineering

Role details

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?

This role is part of Alcon's Engineering function, a team focused on improving quality, processes, products, packaging and materials across our business to help deliver brilliant outcomes.

The Molding Engineer II, Molding & Tooling, is primarily responsible for assisting in mold tooling development by analyzing injection molding parameters and optimizing processes. You will support defect troubleshooting, quality control, and process efficiency enhancements while collaborating with engineers to refine mold designs and improve manufacturability at our Manufacturing Facility in Houston, TX. Specifics include:

• Lead molding engineering and validation activities across new product introductions, remediation efforts, and sustaining manufacturing programs, ensuring alignment with business objectives, regulatory requirements, and project timelines.
• Serve as the technical subject matter expert for injection molding processes, thermoplastic and LSR, driving data-based analysis, process optimization, troubleshooting, and implementation of robust manufacturing controls.
• Own and drive quality system deliverables across multiple platforms, including Kneat, Teamcenter, NCI investigations, CAPAs, Change Controls, and validation documentation, ensuring compliance, timely execution, and cross-functional alignment.
• Develop, govern, and execute validation strategies and roadmaps, ensuring successful completion of IQ, OQ, PQ, TMV, and process validation activities while mitigating project risks.
• Lead complex defect investigations and root cause analysis efforts, implementing sustainable corrective and preventive actions to improve product quality, process capability, and operational performance.
• Drive process optimization initiatives focused on cycle time reduction, yield improvement, scrap reduction, OEE enhancement, and overall manufacturing efficiency.
• Partner with Tooling, Product Development, Quality, Manufacturing, and external suppliers to optimize mold designs, processing windows, and product manufacturability throughout the product lifecycle.
• Champion continuous improvement initiatives utilizing Lean Manufacturing, Six Sigma, and data-driven methodologies to deliver measurable improvements in safety, quality, delivery, and cost.
• Provide leadership for project planning and execution by developing project plans, tracking deliverables, managing risks, escalating issues appropriately, and ensuring achievement of critical milestones.
• Coach and mentor engineers, technicians, and cross-functional team members while promoting technical excellence, knowledge sharing, and organizational capability development.
• Author, review, approve, and maintain technical and quality documentation in accordance with internal procedures, regulatory requirements, and quality system expectations using Microsoft Office, Kneat, Teamcenter, and Veeva platforms.
• Lead creation, revision, and approval of controlled documents within Veeva QualityDocs, including procedures, work instructions, validation protocols, reports, and Documentation Change Controls (DCCs).
• Represent Molding Engineering during audits, inspections, management reviews, and cross-functional governance meetings, ensuring readiness and compliance with applicable regulatory standards.
• Ensure full compliance with GxP requirements through adherence to approved procedures, accurate documentation practices, data integrity expectations, training requirements, and quality system policies.
• Maintain accountability for individual performance, project execution, and organizational compliance while fostering a culture of safety, quality, continuous improvement, and operational excellence.

WHAT YOU’LL BRING TO ALCON

• Bachelor’s Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6yrs; M.S.+0 yrs)
• The ability to fluently read, write, understand and communicate in English
• 2 Years of relevant experience
• 1 Years of demonstrated leadership
• Work Hours: Monday – Friday, 7:00 AM – 4:00 PM CST
• Location: Onsite
• Travel Requirements: Up to 10%
• Relocation Assistance: None
• Sponsorship Available: No

PREFERRED

• Liquid Silicone Rubber experience
• Project Management experience
• Molding process development and troubleshooting

HOW YOU CAN THRIVE AT ALCON

• Collaborate with teammates to share standard processes and learnings as work evolves!
• Join Alcon’s mission to provide top-tier, innovative products and solutions to enhance sight & enhance lives.
• Grow your career in a highly collaborative and diverse environment.
• Alcon provides robust benefits package including health, life, retirement, flexible time off for salaried associates, paid time off for hourly associates and much more!

Alcon Careers

See your impact at alcon.com/careers

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

Find Jobs for Employees

Find Jobs for Contingent Worker

*ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY*

*Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to* *[email protected]* *and let us know the nature of your request and your contact information.*