Manufacturing Validation Engineer - Tech Transfer

Alcon

Batam

On-site

IDR 320,000,000 - 520,000,000

Full time

6 days ago
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Job summary

Alcon in Batam, Indonesia, is seeking a Senior Validation Engineer to support the Manufacturing Team. You will implement and execute validation/qualification activities for processes, equipment, computerized systems, and facilities.

The role requires 5–10 years in manufacturing or quality disciplines in medical devices or pharma, a Bachelor's in Science or Engineering, fluent English and local language, and strong skills in writing technical reports and reviewing documentation.

Qualifications

  • Bachelor’s Degree in Science or Engineering.
  • 5–10 years experience in manufacturing/ manufacturing science & technology/quality / technical development in medical device, pharmaceutical manufacturing or food & beverage manufacturing.
  • At least 5 years of experience in executing validation activities in complex projects.
  • Good understanding of requirements and validation lifecycle.
  • Fluent in English and local language.
  • Strong ability in reviewing and writing technical reports.

Responsibilities

  • Execute and support site validation/qualification activities
  • Support Validation Efforts for Tech Transfer projects
  • Preparation, review and remediation of validation protocols
  • Training of validation protocols, site validation SOPs
  • Support validation activities for large capital procurement projects
  • Ensure compliance and provide technical support to the validation team

Skills

Validation lifecycle
Technical report writing
Quality systems
English proficiency
Local language proficiency

Education

Bachelor's Degree in Science or Engineering

Job description

Alcon in Batam, Indonesia, is seeking a Senior Validation Engineer to support the Manufacturing Team. You will implement and execute validation/qualification activities for processes, equipment, computerized systems, and facilities.

The role requires 5–10 years in manufacturing or quality disciplines in medical devices or pharma, a Bachelor's in Science or Engineering, fluent English and local language, and strong skills in writing technical reports and reviewing documentation.

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