For over 25 years, Abcam has been providing tools the scientific community needs to enable faster breakthroughs in critical areas like cancer, neurological disorders, infectious diseases, and metabolic disorders.

We believe that to continue making progress, we need to work together, each bringing our own unique perspectives to make an impact on the world. This community needs people like you: dedicated, agile and above all audacious so we can truly drive science forward.

The Quality Assurance Manager is responsible for overseeing an ISO 9001 certified Quality Management System producing research kits and an ISO 13485 and MDSAP certified division producing Class I IVDs, ensuring compliance and excellence. The Quality Assurance Manager drives quality improvements for our customers across the Americas, fostering a culture of continuous improvement and operational excellence. The Quality Assurance Managers leadership will be pivotal in enhancing customer satisfaction and achieving organizational success.

This position reports to the Vice President of Global Quality Assurance and is part of the Quality Assurance team in Waltham MA and will be on-site.  At Abcam, our vision is to be the most influential life sciences company for researchers worldwide.

In this role, you will have the opportunity to:

• Responsible and Accountable for the Quality Management Systems (QMS) at Abcam’s Waltham area site.
• Assure compliance with applicable regulations, including ISO 13485, 21 CFR 820, ISO 9001 quality standard requirements.
• Maintain knowledge of existing and emerging regulations, standards, and guidance documents and interpret regulatory rules or rule changes and ensure communication through corporate policies and procedures, and engaging training.
• Lead Quality complaint investigations and ensure timely closure for identified Corrective and Preventative Actions to improve overall complaint rate performance for all customers in the Americas
• Direct management of QA Coordinators which develops capability and enables a high performing, engaged quality team.
• Lead the Quality deliverables at the site and influencing all relevant teams to deliver high performance and meet key QA targets through daily management and weekly reviews.
• Promote the development of a company-wide culture of quality assurance and understanding of key QMS elements.

The essential requirements of the job include:

• Education: Bachelor's degree in Quality Management, Engineering, Life Sciences, or a related field.
• Experience: Minimum of 5 years in quality assurance within the medical device or related industry.
• Leadership Experience: At least 3 years of experience in a managerial or supervisory role.
• Regulatory Knowledge: Proficiency in ISO 9001, ISO 13485, and MDSAP standards.
• Analytical Skills: Demonstrated ability to analyze data and proficient with analytical methods like Pareto Charts, Control Charts, Statistical Methods and Sampling Plans.
• Technical Proficiency: Lead Auditor Certification, experience leading investigations and CAPAs, and supporting validation plans, design, and production provision activities.
• Project Management: Experience leading Quality Plans, or Continuous Improvement projects to deliver on-time to defined specifications.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Travel: 5% travel – including potential internationally

It would be a plus if you also possess previous experience in:

• Experience with In Vitro Diagnostic medical devices
• Experience with Immunohistochemistry methods and evaluation

The salary range for this role is $110,000-$120,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and Retirement Benefits to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistancedanaher.com.