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 Associate, Manufacturing Production Process Engineering (Science/Tech/Engineering Path), is primarily responsible for designing, developing, and implementing efficient production processes for mass production. You will conduct tests, troubleshoot issues, and provide guidance on technical specifications, requiring technical skills, problem-solving abilities, and reliability.
Specifics Include:
• Apply technical knowledge to perform tasks and support project goals effectively
• Design, develop, and implement new or revised production processes for efficient mass production, including the arrangement of manufacturing equipment for optimal layout and the sequence of production operations
• Specify procedures for fabricating applicable tools and equipment and adapt machinery in response to factory conditions
• Conduct tests throughout all production stages to control variables and solve production problems
• Provide guidance to product design engineering on technical specifications to best use equipment and manufacturing techniques
• Ensure production processes and procedures comply with regulations, adhering to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate documentation, ensuring quality control, and completing required training
• Follow procedures with some decision-making authority, requiring job-related training and attention to detail
• Meet individual job requirements and contribute to overall organizational compliance
• Commit to continuous improvement and regulatory complianceAll associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations .
Qualifications: Associate shall have the appropriate education and experience to successfully perform the responsibilities/activities of this role.
The associate will be responsible for analyzing and optimizing complex medical device manufacturing processes. This includes identifying opportunities for improvement, proposing data‑driven solutions, and implementing manufacturing or design changes to increase yield, throughput, and overall process robustness.
Highly valued: Experience with optics
Soft Skills and Cultural Fit
* Ability to learn quickly and adapt to changing environments
* Commitment to high-quality work and continuous improvement
* Positive attitude and willingness to take on new challenges
* Computer literacy
What We Offer
* Competitive salary and benefits package.
* Opportunities for professional growth and development.
* Inclusive and innovative work environment.
* The chance to make a meaningful impact on global eye health.
All applicants need to have full Australia work rights.
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