Senior Quality Engineer in Massachusetts

Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do...

Bevi is on a mission to disrupt the beverage supply chain and replace single-use water bottles with smart water machines. Thousands of companies use Bevi to sustainably provide their employees with pure, sparkling, and flavored water at work. As the market leader in IoT-enabled beverage machines, we’ve raised over $160M in venture capital and we have grown tremendously each year since launch. In addition to maintaining hypergrowth with our current product line, Bevi is heavily investing in new product development.

We are seeking a Senior Quality Engineer to join Bevi’s manufacturing and quality team. This role reports to the Director of Quality Engineering, and will be responsible for measuring, improving, and maintaining the quality of Bevi’s products. The Senior Quality Engineer will work closely with sustaining and engineering teams to identify and prioritize targets for improvement. The ideal candidate will embrace the Bevi core values, learning new skills,...

Global Life Science Hub are in search of a Senior Quality Assurance Engineer. This dynamic position involves collaborating closely with the engineering and instrument manufacturing departments to ensure product quality and adherence to quality systems.

Key Responsibilities:

• Collect, analyze, and report quality metrics, and develop improvement plans as needed.
• Support process enhancements in Medical Device Software, Hardware, and Cybersecurity.
• Ensure timely resolution of internal and external audit findings.
• Collaborate with teams to create and implement action plans for CAPA, Complaint Investigations, and NCMRs.
• Produce quality reports to monitor cycle times, yield/quality rates, and identify trends using Pareto charts.
• Lead improvements in the Quality System, including requirement definition, system validation, process document updates, and user training.
• Conduct supplier assessments and...

Why Allurion?

We are overjoyed to be recognized as one of Deloitte's top 500 fastest-growing technology companies in the US! But wait, there's even more excitement in store! Get ready for an incredible new journey as we proudly announce our official public listing ALUR. This momentous milestone opens up a new era filled with boundless possibilities and remarkable growth for our company!

At Allurion, our core values of Audacity, Grit, Authenticity, Accountability, and being Data Driven, combined with our passion for innovation, have fuelled our growth and will help us achieve our ambitious mission – ending obesity! As part of a recognized Great Place to Work ® in the US, UK, France, Allurions engage as a collaborative global team while solutioning a critical healthcare challenge which affects millions. We are driven by purpose, motivated by individual challenge and growth, and energized by collective engagement and competitive rewards. We invite you to join us as we...