Validation Engineer

Alcon MX; Batam; On-site; IDR 513,259,195 - 855,431,993; Full time

Job summary

A global health company is seeking a Validation Engineer in Batam, Indonesia. The role involves handling complex tasks in validation including planning and executing studies, conducting risk assessments, and preparing reports. The ideal candidate should have a relevant degree and experience in aligning practices with GxP regulations. This position requires strong problem-solving skills and collaboration across teams to maintain compliance and quality standards.

Qualifications

• Handle and contribute to advanced projects in the Validation discipline.
• Plan, execute, and document validation studies.
• Support validation activities for aseptic process management.

Responsibilities

• Conduct risk assessments and design protocols.
• Review and approve change control documentation.
• Collaborate with cross-functional teams for problem-solving.

Skills

Complex task handling

Risk assessment

Data analysis

Problem-solving

Education

Relevant degree in Science/Technology/Engineering

Job description

Validation Engineer page is loaded## Validation Engineerremote type: Not applicablelocations: Batam, Indonesiatime type: Full timeposted on: Posted Todaytime left to apply: End Date: August 31, 2026 (30+ days left to apply)job requisition id: R-2025-44066This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly.The Associate II, Validation (Science/Tech/Engineering Path), is primarily responsible for handling complex tasks in the Validation discipline, including planning, executing, and documenting validation studies, conducting risk assessments, and preparing reports. You will make significant decisions and support validation activities. Specifics Include: • Handle complex tasks and contribute to advanced projects in the Validation discipline • Plan, execute, and document validation studies to ensure equipment, systems, and processes operate effectively and comply with regulations • Conduct risk assessments, design protocols, analyze data, and prepare validation and qualification reports • Make significant decisions within your project area, influencing outcomes with enhanced technical skills and problem-solving abilities • Support validation activities for aseptic process management • Review and approve change control documentation • Provide audit support and collaborate with cross-functional teams to drive problem-solving and innovation • Adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate documentation, ensuring quality control, and completing required training • Commit to continuous improvement and regulatory compliance, meeting individual job requirements and contributing to overall organizational compliance.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. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations. Qualifications: Associate shall have the appropriate education and experience to successfully perform the responsibilities/activities of this role.**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.