Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

• Determine and implement quality assurance procedures, processes, and standards
• Collaborate with various teams to ensure flawless execution of quality control activities
• Conduct rigorous testing and analysis to identify areas for improvement and optimization
• Monitor and collaborate with team members for daily operational compliance to the quality management system (QMS) and other Regulatory, ISO, and international standards.
• Improve product and process quality through direct support and monitoring of value stream production and new development.
• Lead and support the investigation of nonconformance, audit findings, CAPA's, complaints, environmental alerts and SCAR's by conducting CAPA investigations, risk assessment (FMEA, DFMEA, PFMEA), root cause analysis and effectivity checks.
• Assist with the preparation and approval of change control documents related to the operation and improvement of Operations processes.
• Compete in a fast-paced environment to meet strict deadlines
• Conduct internal and participate in external Quality System audits to assess the compliance with the QMS, FDA regulations, ISO standards, EU IVDR and any other international regulations and internal requirements.
• Successfully implement continuous improvement initiatives to enhance overall quality and efficiency

• Bachelor's degree in engineering or a related field, and 5 years of relevant experience; OR Master degree and 3 years of experience.
• Understanding of global regulatory and quality requirements associated with medical devices such as ISO 13485, ISO 14971, 21 CFR Part 820
• Knowledge of IVDR and MDR, a plus.
• Experience working in a liquid formulation and fill operation, a plus
• ASQ certified quality engineer, ASQ certified quality auditor, and/or Six Sigma/Lean certified, a plus