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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.
As a Quality Engineer you are tasked to focus on designing, developing, and implementing new or revised production processes for the efficient/economical mass production of goods at Batam. In this role, a typical day will include:
Responsibilities:
Manage GxP and validation/qualification activities.
Ensure GMP compliance and provide technical support to DHR/QA/Production.
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.
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Find Jobs for Contingent Worker
As a Quality Engineer you are tasked to focus on designing, developing, and implementing new or revised production processes for the efficient/economical mass production of goods at Batam. In this role, a typical day will include:
Responsibilities:
- Manufacturing Production Process Engineering focuses on designing, developing, and implementing new or revised production processes for the efficient/economical mass production of goods including:
- Designing arrangement of manufacturing equipment to ensure most efficient and productive layout
- Designing the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery in response to factory conditions
- Conducting tests throughout all stages of production to determine control over applicable variables and troubleshooting/solving production problems
- Providing guidance to product design engineering on technical specifications that will best utilize equipment and manufacturing techniques
- Ensuring that production processes and procedures are in compliance with regulations
- Responsible to assist and support Failure Investigation, root cause analysis, generation and execution of corrective and preventive actions.
- Responsible to manage and support validation/qualification activities for new product/process/raw material/computer systems qualification.
- Support and coordinate re-evaluation activities for existing/legacy systems.
- Responsible to ensure compliance and provide guidance plus technical support to QA/DHR/Manufacturing.
- Responsible to perform product/process and system risk assessment.
- Responsible to lead and drive Quality and compliance Improvement Program and support Continuous Improvement Plan (CIP) using LEAN and SIX SIGMA principles.
- Lead/support Failure Investigation and root cause analysis, generation and execution of corrective and preventive actions.
- Manage GxP and validation/qualification activities.
- Ensure GMP compliance and provide technical support to DHR/QA/Production.
- Minimum Degree in Science/Engineering or related studies.
- 1-2 Years of Experience in Pharmaceutical / Medical Device Industry preferred
- 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.
Manage GxP and validation/qualification activities.
Ensure GMP compliance and provide technical support to DHR/QA/Production.
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
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