Job details Spherion is seeking a qualified and detail-oriented Validation Engineer to join a team in a dynamic and growing medical device environment.

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.

Working hours: 8:00 AM - 5:00 PM

Skills: 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).

Education: Bachelors

Experience: 4-7 years

Qualifications: BA 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.