Nova Biomedical: One Global Brand. One Vision. Together under one name.
Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical , marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets.
About the company
At Nova Biomedical, we're not just building instruments, we're powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care.
Our integration brings together more than 70 years of scientific excellence with Nova's cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we're setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.
With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we're building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity .
Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you'll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health.
Explore what's next with us at novabiomedical.com or aicompanies.com
About the role
The Senior Director of Quality focuses on assuring company compliance to ISO/FDA QSR, IVDD, IVDR, ISO 13485, ISO 14971; Direct oversight of CAPA management, ISO/QSR employee training; metrics; validation, internal and external quality auditing processes; improvements. Primary responsibilities includes managing corporate level compliance activities along with day-to-day quality activities at the global Nova Biomedical manufacturing sites. Interact directly with management at other Nova subsidiaries on issues regarding QA systems and processes.
If you're passionate about quality assurance and want to be part of a team that is shaping the future of life sciences, we'd love to hear from you, apply today!
What you'll do
Provide leadership and support during external audits performed by regulatory bodies such as the FDA and TUV, Partners and Customers, as well as other auditing bodies
Support conducting internal audits of Nova's Quality System
CAPA management of internal and external CAPAs for appropriate action, risk assessment, and effectivityServes as Nova's PLQC chair
Management and execution of NIRs and other failure investigations
Manage the Nova Shipping Hold processes and ensure timely interaction between functional groups
Employee Quality Training design and delivery for company-wide compliance
Oversight of approval process for NCMRs as part of the MRB process
Supplier Quality Engineering support for review and approval of SQE CAPAs
Provide quality leadership of company improvement projects
Oversee validation activities and ensure effectiveness of process
Ensure compliance with company procedures and processes
Quality Planning - develop and execute plans related to product development as well as new project plans
Oversee metrics and KPIs for evaluation and reporting at Senior Management Reviews
Ensure timely response and feedback to Nova's suppliers and ensure supplier-related issues are resolved in a manner that does not disrupt production processes
Management of customer and partner qualifications, and ongoing compliance maintenance activities, such as SCARs, quality surveys, and quality agreements
Provide quality support to Nova's subsidiaries
Management of documents of external origin (i.e. ISO Standards, Electrical Standards, etc.)
What we are looking for in you
Certifications are not required. However, Certified Quality Auditor and/or Certified Quality Manager through ASQ is a plus
Strength in organizational skills
Proven track record with process improvements
Communication with various functional departments will be critical to achieving successful outcomes
Strong communication and presentation skills
Working knowledge of GMP is required
Demonstrated ability to provide Root Cause Analysis tools and structured problem-solving methodologies to QMS issues
Skilled at performing and leading internal and external audits
Technical knowledge of Nova-type products is a plus
Knowledge of LMS software
12+ years of medical diagnostic or device experience managing a quality program
12+ years of quality team management
BS Degree in the sciences or other technical discipline, or 10+ years of QA experience in the medical device or diagnostic industry
Physical Requirements for this role include:
The ability to work while standing or sitting for prolonged periods
The ability to work on a laptop or desktop computer for prolonged periods
The full list of physical requirements for this role is available upon request.
Why work for Nova Biomedical
Flexible Medical, Dental, & Vision Coverage
Competitive 401k company match
Bonus Program, Generous PTO and paid holidays
Generous Tuition reimbursement
Hybrid and flexible work arrangements
Professional development, engagement and events
Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices
Company subsidized cafeteria in our Waltham, MA office
Work Location: Hybrid work schedule, onsite in our Waltham, MA office
Targeted Salary Range: $220,000 - $300,000/year
Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate's experience and may vary based on individual factors such as location, skills, and education.
EEO Statement:
Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Privacy policy
Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical , marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets.
About the company
At Nova Biomedical, we're not just building instruments, we're powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care.
Our integration brings together more than 70 years of scientific excellence with Nova's cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we're setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.
With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we're building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity .
Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you'll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health.
Explore what's next with us at novabiomedical.com or aicompanies.com
About the role
The Senior Director of Quality focuses on assuring company compliance to ISO/FDA QSR, IVDD, IVDR, ISO 13485, ISO 14971; Direct oversight of CAPA management, ISO/QSR employee training; metrics; validation, internal and external quality auditing processes; improvements. Primary responsibilities includes managing corporate level compliance activities along with day-to-day quality activities at the global Nova Biomedical manufacturing sites. Interact directly with management at other Nova subsidiaries on issues regarding QA systems and processes.
If you're passionate about quality assurance and want to be part of a team that is shaping the future of life sciences, we'd love to hear from you, apply today!
What you'll do
Provide leadership and support during external audits performed by regulatory bodies such as the FDA and TUV, Partners and Customers, as well as other auditing bodies
Support conducting internal audits of Nova's Quality System
CAPA management of internal and external CAPAs for appropriate action, risk assessment, and effectivityServes as Nova's PLQC chair
Management and execution of NIRs and other failure investigations
Manage the Nova Shipping Hold processes and ensure timely interaction between functional groups
Employee Quality Training design and delivery for company-wide compliance
Oversight of approval process for NCMRs as part of the MRB process
Supplier Quality Engineering support for review and approval of SQE CAPAs
Provide quality leadership of company improvement projects
Oversee validation activities and ensure effectiveness of process
Ensure compliance with company procedures and processes
Quality Planning - develop and execute plans related to product development as well as new project plans
Oversee metrics and KPIs for evaluation and reporting at Senior Management Reviews
Ensure timely response and feedback to Nova's suppliers and ensure supplier-related issues are resolved in a manner that does not disrupt production processes
Management of customer and partner qualifications, and ongoing compliance maintenance activities, such as SCARs, quality surveys, and quality agreements
Provide quality support to Nova's subsidiaries
Management of documents of external origin (i.e. ISO Standards, Electrical Standards, etc.)
What we are looking for in you
Certifications are not required. However, Certified Quality Auditor and/or Certified Quality Manager through ASQ is a plus
Strength in organizational skills
Proven track record with process improvements
Communication with various functional departments will be critical to achieving successful outcomes
Strong communication and presentation skills
Working knowledge of GMP is required
Demonstrated ability to provide Root Cause Analysis tools and structured problem-solving methodologies to QMS issues
Skilled at performing and leading internal and external audits
Technical knowledge of Nova-type products is a plus
Knowledge of LMS software
12+ years of medical diagnostic or device experience managing a quality program
12+ years of quality team management
BS Degree in the sciences or other technical discipline, or 10+ years of QA experience in the medical device or diagnostic industry
Physical Requirements for this role include:
The ability to work while standing or sitting for prolonged periods
The ability to work on a laptop or desktop computer for prolonged periods
The full list of physical requirements for this role is available upon request.
Why work for Nova Biomedical
Flexible Medical, Dental, & Vision Coverage
Competitive 401k company match
Bonus Program, Generous PTO and paid holidays
Generous Tuition reimbursement
Hybrid and flexible work arrangements
Professional development, engagement and events
Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices
Company subsidized cafeteria in our Waltham, MA office
Work Location: Hybrid work schedule, onsite in our Waltham, MA office
Targeted Salary Range: $220,000 - $300,000/year
Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate's experience and may vary based on individual factors such as location, skills, and education.
EEO Statement:
Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Privacy policy
Job ID: 520850600
Originally Posted on: 5/12/2026
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