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Quality Assurance Program Manager Jobs in Worcester, MA

Provides oversight of quality management system operations and maintains and operates the Internal Quality Audit Program. * Manages correspondence with suppliers/vendors for all quality assurance ...

Quality Assurance Associate Make Quality Your Impact Are you detail-oriented, dependable, and ... Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a ...

Quality Assurance Associate The Quality Assurance Associate will be responsible for performing in ... Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a ...

[Job Summary] R&R Responsible for coordination, implementation, and maintenance of QA Program. Supervise daily QC Technician Activities. Responsible for identifying quality and food safety issues ...

[Job Summary] R&R Responsible for coordination, implementation, and maintenance of QA Program. Supervise daily QC Technician Activities. Responsible for identifying quality and food safety issues ...

Showing results 21-40

Quality Assurance Program Manager information

See Worcester, MA salary details

$37.9K

$117.8K

$178.6K

How much do quality assurance program manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for quality assurance program manager in Worcester, MA is $117,817.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,800.00 and $144,200.00 per year, depending on experience, location, and employer.

What does a quality assurance program manager do?

A Quality Assurance Program Manager oversees the development and implementation of quality assurance processes within an organization. They ensure that products or services meet established standards of quality, reliability, and performance. This role involves coordinating QA teams, developing testing strategies, analyzing data, and working closely with other departments to resolve quality issues. They also play a key role in continuous improvement by identifying trends and recommending process enhancements. Ultimately, they help ensure customer satisfaction and regulatory compliance.

What are the key skills and qualifications needed to thrive as a quality assurance program manager?

To thrive as a Quality Assurance Program Manager, you need expertise in quality management systems, process improvement, and a relevant bachelor's degree, often in engineering or a related field. Familiarity with tools like ISO 9001 standards, Six Sigma methodologies, and QA software platforms such as Jira or Quality Center is typically required, along with certifications like ASQ or Six Sigma Black Belt. Strong leadership, analytical thinking, and effective communication skills help you manage teams and collaborate across departments. These skills ensure that quality standards are met, risks are mitigated, and products or services consistently meet customer and regulatory requirements.

How does a quality assurance program manager typically collaborate with cross-functional teams to ensure product quality?

A Quality Assurance Program Manager frequently partners with departments such as product development, engineering, and operations to embed quality standards throughout the product lifecycle. They facilitate regular meetings, coordinate testing schedules, and align on quality metrics to ensure everyone is working toward the same goals. This collaborative approach helps quickly identify and address potential issues, streamlining the path to consistent, high-quality outcomes. Effective communication and relationship-building are essential skills for managing these cross-functional efforts.

What is the difference between Quality Assurance Program Manager vs Quality Control Supervisor?

AspectQuality Assurance Program ManagerQuality Control Supervisor
CertificationsASQ CQE, Six Sigma, PMPISO 9001, Six Sigma, CQE (optional)
Work EnvironmentOversees quality systems across departments, strategic planningSupervises daily inspection and testing activities
Employer & Industry UsageManufacturing, aerospace, healthcare, softwareManufacturing, production, industrial settings

The Quality Assurance Program Manager focuses on developing and maintaining quality systems and processes, ensuring compliance and continuous improvement. In contrast, the Quality Control Supervisor manages daily inspection and testing to ensure products meet quality standards. Both roles are essential in quality management but differ in scope and responsibilities.

Is a quality assurance program manager a stressful job?

A quality assurance program manager role can be stressful due to the responsibility of ensuring product quality, meeting deadlines, and managing cross-functional teams. The job often requires attention to detail, problem-solving skills, and the ability to handle pressure during audits or product launches.

What are popular job titles related to Quality Assurance Program Manager jobs in Worcester, MA?

For Quality Assurance Program Manager jobs in Worcester, MA, the most frequently searched job titles are:

What job categories do people searching Quality Assurance Program Manager jobs in Worcester, MA look for?

The top searched job categories for Quality Assurance Program Manager jobs in Worcester, MA are:

What cities near Worcester, MA are hiring for Quality Assurance Program Manager jobs?

Cities near Worcester, MA with the most Quality Assurance Program Manager job openings:

Infographic showing various Quality Assurance Program Manager job openings in Worcester, MA as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $117,817 per year, or $56.6 per hour.

Principal Clinical Quality Assurance Specialist

Boston Scientific

Marlborough, MA • Hybrid

$37.75 - $50.50/hr

Full-time

Re-posted 2 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers


Job description

Additional Location(s): US-MA-Marlborough; US-MN-Arden Hills; US-MN-Maple Grove

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.           

About the role:

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

As a Principal Clinical Quality Assurance Specialist, you will support the internal clinical quality assurance program for your assigned business area, partnering with cross-functional teams to ensure clinical investigations comply with applicable regulatory requirements, Good Clinical Practice (GCP) and Boston Scientific policies and procedures. In this role, you will serve as the Clinical Quality Assurance representative on clinical project teams, conduct internal and external quality audits, and support inspection readiness, corrective and preventive action (CAPA) activities, and clinical acquisition integrations.

Work model, sponsorship, relocation:

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to work from one of our local offices at least three days per week. This position may be based in Marlborough, Massachusetts; Arden Hills, Minnesota; or Maple Grove, Minnesota.

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Your responsibilities will include:

● Serve as the Clinical Quality Assurance representative on clinical project teams, promoting a continuous state of inspection readiness.

● Plan, schedule and conduct internal and external quality assurance audits of clinical systems, investigative sites, processes and controls supporting clinical trials.

● Assess compliance with study protocols, GCP, applicable regulatory requirements and Boston Scientific policies and procedures.

● Evaluate the accuracy, integrity and quality of clinical data generated during clinical investigations.

● Communicate audit observations, evaluate responses, monitor corrective actions and ensure timely closure of audit findings.

● Support investigator sites during regulatory inspections, including preparation activities and responses to inspection findings.

● Contribute to the development and continuous improvement of Clinical QA processes, audit procedures and annual audit planning.

● Support clinical CAPA activities by partnering with CAPA owners and providing quality guidance.

● Represent Clinical Quality during acquisitions and integration activities by identifying risks, supporting sponsorship transfers and ensuring compliance with quality systems and regulatory requirements.

● Demonstrate a commitment to patient safety and product quality by maintaining compliance with the Boston Scientific Quality System and participating in internal quality and supplier audits.

Qualifications:

Required qualifications:

● Bachelor's degree in science, engineering, health sciences or a related discipline.

● Minimum of 5 years' experience in Clinical Quality Assurance, clinical research compliance or a related quality function.

● Minimum of 5 years' experience conducting GCP audits, clinical research audits or other regulated quality audits.

● Working knowledge of ISO 14155, ISO 13485, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).

● Experience supporting quality systems, controlled processes, CAPA and regulatory compliance activities.

● Ability to travel up to 30%.

Preferred qualifications:

● Working knowledge of U.S. and international regulations and standards applicable to clinical research.

● Professional quality certifications, such as ASQ, SOCRA, RQAP-GCP or Certified Lead Internal Auditor.

● Experience collaborating with cross-functional stakeholders in support of clinical quality initiatives, inspections or acquisitions.

● Advanced degree in a scientific, engineering or health-related discipline.

#LI-Hybrid

Requisition ID: 631122 

Minimum Salary: $ 116600 

Maximum Salary: $ 221500 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company 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.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.  


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About Boston Scientific

Sourced by ZipRecruiter

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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