Technician II, Molding Production
Alcon
This listing was originally posted on Alcon's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moAt 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.
As a Technician II supporting Molding Production, you will be trusted for handling complex tasks related to operating molding tools and equipment with minimal supervision. You will conduct quality inspections, handle materials, operate automated equipment, and resolve issues. This role involves mold changes, collaborating with various departments, and troubleshooting medical device molds, requiring advanced technical skills, problem-solving abilities, and effective communication to maintain high production standards and efficiency at Johor, Malaysia.
Job responsibilities:
Handle complex tasks related to operating molding tools and equipment with minimal supervision
Conduct quality inspections using gauges and fixtures, and monitor quality statistically to ensure compliance with standards
Follow work instructions and Good Manufacturing Practice/Good Documentation Practice (GMP/GDP) requirements
Handle materials and operate automated equipment
Resolve issues as they arise
Perform mold changes and collaborate with various departments
Troubleshoot medical device molds
Conduct optical tool inspection, assembly, set-up, targeting, line clearance, mechanical and negative checks, and changeover
Operate the solvent supply and disposal system for production and research
Maintain accurate and complete documentation
Ensure rigorous quality control and complete all required training
Meet individual job requirements and contribute to the overall compliance of the organization
Commit to continuous improvement and compliance with regulatory requirements
Adhere to Good Practice (GxP) regulations by strictly following Standard Operating Procedures (SOPs)
Minimum requirement:
General Certificate in any related field
No experience required, candidate with relevant work experience would have advantage.
Must be willing to work in 12 hours weekly rotating shift.
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BIOTECHNOLOGY
Eye-Care Products
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