Engineer/Scientist I, QC

at  Thermo Fisher Scientific

ENGINEER/SCIENTIST I, QC

Thermo Fisher Scientific is seeking an Engineer/Scientist I, QC with a track record of displaying exceptional work behaviors. Join our world-class Ion Torrent Quality Control department in South San Francisco and be a key member of our team. Your role will be crucial in upholding the flawless quality of our products and ensuring strict compliance with industry standards and regulations. This role offers an ambitious opportunity to apply your proven expertise in a dynamic and challenging setting.

JOB REQUIREMENTS:

• Bachelor’s degree in Chemistry, Biology, Biotechnology, Bioengineering, or a related field, or equivalent experience in the industry.
• Experience working in a Chemistry, Biology, or equivalent laboratory.
• Knowledge in lab protocols and the use of laboratory equipment/supplies to conduct tests.
• Excellent analytical, problem-solving, communication, and teamwork skills.
• Impeccable attention to detail and a commitment to maintaining a high level of accuracy.
• Ability to effectively prioritize assignments and manage projects in a time-sensitive manner.
• Proficiency with Excel and other similar data analysis tools.

Thermo Fisher Scientific Inc. is an equal opportunity employer that values diversity and inclusion. We are dedicated to providing reasonable accommodations to individuals with disabilities throughout the application process. Our commitment to inclusion and collaboration makes us excited to receive your application. Start your exceptional story with Thermo Fisher Scientific today by applying at http://jobs.thermofisher.com.

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• Conduct functional QC of NGS Reagents Kits and sensors (raw materials, in-process products, and finished goods) to maintain the highest quality and compliance.
• Document, compute, and compile data to provide a comprehensive assessment of product performance.
• Maintain accurate and detailed QC batch records and files according to the most stringent quality standards, including ISO compliance and GLP/GMP requirements.
• Generate nonconformance reports in the event of product failure and promptly notify the appropriate parties.
• Actively participate in team meetings to collaboratively troubleshoot product performance and process issues as they arise.
• Conduct methodical troubleshooting experiments to accurately identify the underlying cause of laboratory results that deviate from specifications (out-of-specification or OOS), and implement necessary corrective measures while strictly following established protocols.
• Assist in the development and successful implementation of new QC testing methods and standards.
• Prepare meticulous validation protocols and reports, ensuring they meet our internal quality guidelines.
• Contribute to the submission of essential documents to the Quality Management System.