Senior Associate, Validation Engineering

Alcon; Singapore; On-site; SGD 70,000 - 110,000; Full time

Job summary

Alcon is seeking a Senior Associate, Validation in Singapore to oversee design control and lifecycle management at site. You will liaise with R&D for transfer of technical documentation and conduct risk reviews across products within scope, ensuring rigorous quality and regulatory adherence.

The role requires strong validation experience, aseptic knowledge, and ability to coordinate with cross-functional teams to drive knowledge sharing and continuous improvement.

Qualifications

• Bachelor’s or higher in engineering, sciences, or equivalent
• Minimum 5 years of relevant validation experience
• Knowledge of aseptic and sterilization processes
• Ability to provide after-hours support for validation activities

Responsibilities

• Oversee design control and lifecycle management for site products
• Liaise with R&D for transfer of technical documentation
• Lead transfer of technical documentation related to design control and risk management
• Ensure compliance with GxP and SOPs across projects
• Engage with cross-functional teams including QA, QC, and commercial

Skills

Validation experience

GxP knowledge

Documentation

Education

Engineering or science degree

Job description

At Alcon, we are driven by themeaningful 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 careerlike never before. Together, we go above and beyond to make an impact in thelives of our patients and customers. We foster an inclusive culture and arelooking for diverse, talented people to join Alcon.

As the Senior Associate, Validation under MS&T Team, youwill be responsible to maintain the design control of the products andowns the lifecycle management process of the products at site. You will beresponsible to liaise with R&D for the transfer of technical documentationrelating to design control and risk management review of the products in scope.Ensures seamless flow of knowledge and information across functions, and withother sites when applicable. Responsible for Technical Transfer activities atsite level, including any scale-up.

In thisrole, a typical day will include:

• Oversee multiple technical projects, ensuringgoals are met through specialized expertise and technological innovation
• Develop, implement, and evaluate new productionmaterials, equipment, and technologies before mass production
• Complete manufacturing research and developmentto solve problems related to production cost and quality
• Conduct technical feasibility tests to ensureproduction efficiency
• Evaluate project capacity as the basis forproduction process design and development
• Develop and implement standard manufacturingprocedures
• Evaluate production processes to reduce overallcosts and determine product quality standards
• Arrange equipment and tools to supportproduction
• Select and communicate with vendors to determineproduct specifications and ensure timely and budget-compliant delivery
• Engage with partner functions such as Researchand Development, commercial, and quality
• Make recommendations affecting project outcomes,requiring advanced problem-solving and technical expertise
• Stay current with advances in the field and takean agile approach to problem-solving by testing, iterating, and refiningsolutions
• Adhere to Good Practice (GxP) regulations bystrictly following Standard Operating Procedures (SOPs), maintaining accurateand complete documentation, ensuring rigorous quality control, and completingall required training
• Commit to continuous improvement and compliancewith regulatory requirementsAll associates must adhere to GxP regulations bystrictly following Standard Operating Procedures (SOPs), maintaining accurateand complete documentation, ensuring rigorous quality control, and completingall required training. Associates are responsible for meeting their individualjob requirements and contributing to the overall compliance oftheorganization. Compliance with regulatory requirements and a commitment tocontinuous improvement are essential to our operations .

What You'llBring to Alcon

• Degree in Engineering or scientificfield
• Min 5 years of relevant workexperience in validation activities
• Knowledge in aseptic and sterilization
• Able to provide after office hourssupport for validation related activities when required

HOW YOU CANTHRIVE AT ALCON:

• At Alcon, we are committed to fostering a workenvironment where our employees can grow, innovate, and excel. Here’s how youcan thrive in your role with us:
• Career Growth & Development – Gain access tocontinuous learning opportunities, leadership training, and career advancementprograms to support your professional journey.
• Collaborative Culture – Work alongside passionateand diverse teams in a dynamic and inclusive environment that encouragesinnovation and teamwork.
• Impactful Work – Be part of a purpose-drivencompany that is improving lives by advancing eye care solutions worldwide.
• Recognition & Rewards – Your contributions arevalued and recognized through competitive compensation, performance incentivesand career progression opportunities.
• Global Exposure – Join a world-class organizationwith opportunities to collaborate across international teams and gain globalindustry insights.
• Work-Life Balance & Well-Being – Enjoy employeewellness programs, flexible work arrangements and initiatives that support yourwell-being.

At Alcon, we empower our people to make a difference while growing theircareers in an exciting and supportive environment. Join us and see brilliancein every opportunity!