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Open nowFirst seen 38 hours ago

Senior Validation Engineer

Vinarco133 open roles

Where
Lamphun, Thailand
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Your applicationOpen nowSenior Validation EngineerVinarco · Lamphun, Thailand

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The clock on this job

Early applications get read.

11.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.4%3 days
  3. 11.8%7 days
  4. 18.6%14 days
  5. 35.6%30 days
  6. 45.1%60 days
This job: first seen 38 hours ago

The posting

Our client is a Medical Device 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%.
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