Associate II, Molding & Tooling Engineering

AlconHouston, TX
Onsite

About The Position

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 II, Manufacturing Science & Technology Engineering is primarily responsible for developing and evaluating new production materials, equipment, and technologies. You will conduct research, feasibility tests, and process design, requiring advanced knowledge and problem-solving skills at our Manufacturing Facility in Houston, TX.

Requirements

  • Bachelor’s Degree or Equivalent years of directly related experience (or high school +8 yrs; Assoc.+4 yrs)
  • The ability to fluently read, write, understand and communicate in English

Responsibilities

  • Support molding engineering and validation activities across new and existing programs.
  • Assist in conducting analysis on injection molding parameters and process optimization.
  • Support and drive quality deliverables across multiple quality systems, including (but not limited to) Kneat, Teamcenter, NCI investigations, and CAPA identification, ensuring cross‑functional alignment.
  • Support the development and execute validation roadmaps, ensuring timely completion of all validation tasks and milestones.
  • Support defect troubleshooting, quality control implementation, and ensure rigorous quality control.
  • Enhance process efficiency and improve cycle times.
  • Collaborate with engineers to refine mold designs and enhance part manufacturability.
  • Drive continuous improvement initiatives by identifying and implementing efficiency gains across molding engineering and production operations.
  • Support leadership in task tracking, project timeline management, and delivery of critical project outcomes.
  • Create, revise, and maintain documentation using Microsoft Office tools in compliance with regulatory and quality system requirements.
  • Utilize Veeva Quality Docs to author new procedures, manage controlled document uploads, and initiate and process Documentation Change Controls (DCCs).
  • All 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.
  • Adhere to Good Practice regulations by following Standard Operating Procedures, maintaining documentation, ensuring quality control, and completing required training.
  • Meet individual job requirements and contribute to organizational compliance.
  • Commit to continuous improvement and regulatory compliance.

Benefits

  • health
  • life
  • retirement
  • flexible time off for salaried associates
  • paid time off for hourly associates
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