Global Professionals

As a former SQA client of 10 years, I decided to become an associate in 2016. At that time, becoming an SQA Associate was the next logical career progression for me. Using my supplier quality management background, spanning 33 years in Aviation, Space, Defense, Medical Device and Pharma, SQA enabled me to contribute to SQA’s equally diverse client base, fulfilling roles in auditing, Project Management and consulting.

Recently, I have been more actively engaged with the SQA – Pfizer partnership conducting many onsite audits for a wide range of materials and products. Not only does this activity fulfill a necessary function for the SQA – Pfizer partnership, it also stretches me to learn so many different approaches to solving similar supplier issues.

As I head into the twilight of my profession, I could not ask for a better suited role to be performing, or the partnership I have with SQA.

I have worked for many years as a quality assurance engineer and manager for a manufacturer that develops and manufactures space systems and equipment. I am currently assisting a U.S. satellite system manufacturer with inspections of their subcontractors in Japan. In the space industry, the contractor is contracted to perform inspections at key events during subcontractor manufacturing and testing. I live in Japan, and by performing inspections in Japan on behalf of the contractor, I help the contractor reduce costs and maintain quality.

An experienced quality management professional with over 15 years of expertise in a leading multinational company, demonstrating strong leadership, analytical, and communication skills.

With 15 years of experience in the life sciences industry, I specialize in Computerized System Validation (CSV), Project Quality Management (PQM), customer and internal audits, and business and technology consulting. I have deep expertise in the validation of computerized systems within GxP-regulated environments, as well as in risk management, remediation assessments, and optimizing global quality, operations, manufacturing, and IT development processes. Certified as a Quality Auditor (CQA) by the American Society for Quality (ASQ), Certificate #75336, I am skilled in conducting ISO and GxP audits for suppliers to life sciences companies. I have a proven ability to lead cross-functional teams, driving projects to successful completion on time and within budget, leveraging Lean Six Sigma, Agile/Scrum, and Waterfall methodologies. With strong facilitation and coaching skills, I consistently deliver results.

Auditing is my true passion! I am a Doctor of Pharmacy with 20 years of experience in the medical device and pharmaceutical industries, having held various technical and quality-focused roles. My career began in the analytical laboratory, followed by roles in pharmaceutical development and production, and later expanding into the quality management of Class III medical devices. Currently, I work as an independent auditor, specializing in medical device and pharmaceutical supplier and internal audits. I also serve as an auditor for Certification Bodies and Notified Bodies in the medical device sector. My clients often describe me as a collaborative team player with exceptional communication skills. Outside of work, I’m an avid mountain biker and hiker, embracing the outdoors with the same passion I bring to my professional life.

At the core, I’m a proud father of three, and much of my time is dedicated to them. In my spare moments, I’m passionate about college sports and enjoy unwinding with video games. I served 7 years on active duty in the Navy, which was followed by several years as a reservist. Prior to transitioning into my role as Sr. On-Site Program Coordinator, I spent about 15 years in customer service and sales, gaining valuable experience across various levels. In my current role, I am the primary point of contact for a wide range of inspector support services, including IT, payroll, time-off requests, and client data inquiries. At Spirit, my focus is on developing processes where none exist and refining procedures for larger-scale programs, ultimately creating a blueprint for sites to function independently in the future.

Robert Feng joined SQA in 2012 and is one of our leading auditors in China. With 23 years of experience in quality assurance within the pharmaceutical and dietary supplement industries, Robert has conducted over 300 audits for clients in the healthcare sector. His expertise and dedication have made him an invaluable member of our team. Outside of work, Robert enjoys reading, traveling, and swimming. As a qualified and committed SQA Associate, we are proud to have him as part of our team!

SQA has been the biggest part of my independent contractor business. Since partnering with SQA in August 2018, I have completed more than 80 supplier audits and were it not for COVID-19, I expect that number would be 100+. Working as an independent contractor has its rewards and challenges. “Flexibility” is a plus – I work twice as hard and take on as much work as possible, but I also spend more time with my family. I’m very proud of my family, and I’m very happy that, while working 60-80-hour weeks, I have lots of quality time with them. The other plus is that I love the work I do – while helping clients with projects and audits to meet their needs, I’m also continuously learning and making improvements. Thank you, SQA, for helping me make this all possible!