Senior Validation Specialist
3 weeks ago
Key Responsibilities:
- Participate in project teams for new investments and production changes, ensuring seamless integration and quality assurance.
- Develop and implement validation strategies, including planning, documentation, and risk analysis.
- Coordinate the implementation of validation, qualification, and commissioning activities, ensuring compliance with regulatory requirements.
- Conduct requirements definition, risk assessments, and periodic reviews to ensure the validation process is thorough and effective.
- Lead and coordinate independent validation activities throughout the process, ensuring accuracy and attention to detail.
- Review and release validation documents, ensuring they meet quality and regulatory standards.
- Requirements:
- Over 2 years of experience in the medical device or pharmaceutical industry.
- Experience as a Validation Leader or Validation Engineer.
- Technical or scientific university education.
- Knowledge in validation work and statistical tools.
At Thermo Fisher Scientific, we value teamwork, quality, and the exchange of experience. If you are a responsible, driven, and flexible individual with a passion for collaboration and communication, we would love to hear from you.
To be successful in this role, you should have a strong understanding of validation principles and practices, as well as excellent communication and leadership skills.
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