Senior Validation Engineer

Vinarco • English: B2 • Travel required • Bachelor's Degree • 1 day ago

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Salary

≈ $14k – $31k per year (Estimated)

Location

In office (Lamphun)

Seniority

Senior · 3+ years exp

Confirmed on the employer's own hiring board on Oct 20, 2026. First seen by Alion on Oct 19, 2026.

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Vinarco

Vinarco is a recruitment and workforce solutions group based in Bangkok, Thailand, providing permanent recruitment, contracting and manpower supply, manpower relocation, immigration and work permit services and compliance consulting. Established in Asia in 1993, the group has built a network of subsidiaries across Thailand and Southeast Asia, including Kuala Lumpur, and places staff with clients in engineering, construction, oil and gas, renewable energy, manufacturing, logistics and agrochemicals. It recruits accountants, finance managers, sales and business development managers, engineers, logistics and warehouse leads and commissioning staff on behalf of its clients.

vinarco.com • HQ: Bangkok, Thailand • Employer of Record & PEO • Recruiting & Staffing • Est. 1993

Our client is a MedicalDevice Manufacturing Industry.

Position: Senior Validation Engineer

Work Type: Monday Friday (5 Days/Week) Full-time

Location: Lamphun, Thailand Travel Requirement: 10-20%

Job Summary:

We are seeking an experienced Senior Validation Engineer to lead and manage validation activities, ensuring compliance with regulatory standards and company goals. This role oversees validation testing, documentation, and process improvement efforts while coaching and guiding team members.

Key Responsibilities:

Lead and manage validation teams to ensure timely and accurate completion of validation projects.
Develop, implement, and maintain validation systems in compliance with regulatory and internal standards (e.g., ISO13485, FDA, EU).
Provide technical leadership and coaching to ensure quality of validation work and continuous team development.
Ensure all validation activities support regulatory and compliance requirements.
Analyze and understand process control systems to support manufacturing improvements.
Resolve performance or process issues to ensure targets are met.
Collaborate with cross-functional teams including Quality, Engineering, and Production.
Perform additional tasks as assigned to support departmental success.

Qualifications:

Bachelors or Masters degree in Engineering, Science, or related field (e.g., Industrial Engineering, System Engineering, Chemical, Food Science, Pharmaceutical).
3-5 years of experience in Validation, process control, or manufacturing improvement.
Experience in the medical device industry with knowledge of regulatory requirements (ISO13485, FDA, EU MDR) is highly preferred.
Strong understanding of cleanroom and production environment standards.
Experience with Lean Manufacturing and continuous improvement initiatives.
Excellent problem-solving, analytical, and organizational skills.
Strong leadership, team collaboration, and interpersonal communication skills.
Proficient in validation tools/software such as Minitab and Microsoft Office.
Good written and spoken English communication and presentation skills.
Able to travel domestically up to 10-20%.