Staff QA Engineer
As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.
Staff QA Engineer
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.
Join our collaborative team at Thermo Fisher Scientific as a Staff QA Engineer, where you'll contribute to ensuring product quality and regulatory compliance across our operations. You'll work at the intersection of quality assurance, regulatory compliance, and continuous improvement to help deliver life-changing solutions to our customers. Collaborate with cross-functional teams to advance quality initiatives, conduct audits, manage validation activities, and support a culture of excellence. Your expertise will directly impact our mission of enabling customers to make the world healthier, cleaner, and safer through innovative scientific solutions.
REQUIREMENTS:
- Strong knowledge of GMP regulations, ISO standards (9001, 13485), and regulatory requirements (FDA, EMA, etc.)
- Experience conducting internal and external audits, including regulatory inspections and client audits
- Expertise in quality systems including CAPA, change control, document control, and risk management
- Proficiency in quality tools and methodologies (FMEA, root cause analysis, statistical analysis)
- Experience with validation activities (IQ/OQ/PQ, process validation, computer system validation)
- Strong project management and cross-functional team leadership abilities
- Advanced problem-solving and analytical skills with attention to detail
- Excellent written and verbal communication skills
- Experience with quality management software systems (TrackWise, SAP, etc.)
- Knowledge of data integrity requirements and computer system compliance
- Ability to review and approve technical documentation, protocols, and reports
- Experience supporting quality professionals
- Travel up to 25% as required
Education:
- Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of quality assurance experience in regulated environments (pharmaceutical, medical device, or biotech industry)
- Preferred Fields of Study: Engineering, Life Sciences, Chemistry, Biology, or related technical/scientific field
- Additional certifications preferred: ASQ CQE (Certified Quality Engineer), CQA (Certified Quality Auditor), or relevant industry certifications
