Job Description

Spherion is seeking a qualified and detail-oriented Validation Engineer to join a team in a dynamic and growing medical device environment. The ideal candidate will play a critical role in process validation and documentation, ensuring that instrumentation, equipment, and procedures operate efficiently to consistently produce high-quality medical products.

This position is perfect for a hands-on engineer who thrives in collaborative environments, is passionate about quality assurance, and has strong expertise in validation methodologies.

Key Responsibilities:

• Lead and execute equipment and process validation (IQ, OQ, PQ) including full documentation.
• Develop and maintain engineering documents, work instructions (WIs), and validation protocols.
• Monitor, test, and analyze equipment and process performance.
• Document and report test results according to regulatory standards.
• Collaborate cross-functionally to transfer new products and processes into production.
• Ensure continuous improvement and compliance with quality and safety standards.

Qualifications:

• Bachelor’s degree in Mechanical Engineering or Biomedical Engineering (or related field).
• Minimum 5 years of experience in R&D or Engineering roles within the medical device industry.
• Solid understanding of medical device validation processes and related documentation.
• Strong verbal and written communication skills; able to convey complex technical data to diverse audiences.
• Excellent team player with a proactive and positive attitude.
• Fast learner with a high level of attention to detail.
• Fluent in English (both written and verbal).

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