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Senior Validation Engineer II

Job in Batam, Indonesia
Listing for: Alcon
Full Time position
Listed on 2025-12-05
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Validation Engineer, Pharma Engineer
Job Description & How to Apply Below

Job Overview

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.

Role

Senior Validation Engineer II – Manufacturing Team – Batam Plant

Responsibilities
  • Write the validation plan including complex process validations
  • Review validation/qualification written by the Validation Engineers
  • Preparation, review and remediation of validation protocols
  • Takes a leadership role in the project team and project management
  • Communicates with the project team, site management and global project stakeholders
  • Will visit the transferring site to learn the process and become receiving site expert
  • Expected to have an expert level of understanding of validation and strong project management skills
Qualifications
  • Bachelor Degree in Science or Engineering
  • Minimum 8 years experience in manufacturing/manufacturing science & technology/quality/technical development in medical device or pharmaceutical manufacturing
  • Experience in complex projects
  • Experience leading a team of Validation Engineers
  • Deep understanding of Process Validations and Validation types
  • Strong understanding of requirements and regulations of FDA, ISO, etc
  • Fluent in English and local language
  • Strong ability in reviewing and writing technical reports
  • This role will be required to travel
Benefits
  • 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.
Seniority Level

Mid-Senior level

Employment Type

Contract

Job Function

Writing/Editing, Engineering, and Project Management

Industries

Pharmaceutical Manufacturing and Medical Equipment Manufacturing

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Position Requirements
10+ Years work experience
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