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Quality Assurance Program Manager Jobs in Edgartown, MA

Hathaway Manor Extended Care

ACTIVITIES AIDE

New Bedford, MA · On-site

$14.75 - $19.25/hr

... quality assurance program for the activity department. • Perform administrative duties, i.e. completing necessary forms, reports, etc. Opportunities for Growth/Advancement. Equal Opportunity ...

Integritus Healthcar

ACTIVITIES AIDE

New Bedford, MA · On-site

$14.75 - $19.25/hr

... quality assurance program for the activity department. • Perform administrative duties, i.e. completing necessary forms, reports, etc. Opportunities for Growth/Advancement. Equal Opportunity ...

Cape Cod Hospital

Case Manager

Hyannis, MA · On-site

$21.25 - $27.25/hr

Case Manager The Case Manager is responsible for the timely facilitation and coordination of ... Maintains established departmental policies and procedures, objectives, quality assurance program ...

Cape Cod Hospital

Case Manager

Hyannis, MA · On-site

$21.25 - $27.25/hr

Case Manager The Case Manager is responsible for the timely facilitation and coordination of ... Maintains established departmental policies and procedures, objectives, quality assurance program ...

Cape Cod Healthcare Inc.

Case Manager

Hyannis, MA · On-site

$42.04 - $89.99/hr

The Case Manager must assess patient needs utilizing established standards/Care Maps and other ... Maintains established departmental policies and procedures, objectives, quality assurance program ...

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All JobsQuality Assurance Program JobsQuality Assurance Program Manager JobsQuality Assurance Program Manager Jobs in Edgartown, MA

Quality Assurance Program Manager information

See Edgartown, MA salary details

$44.7K

$138.9K

$210.5K

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

As of Sep 4, 2026, the average yearly pay for quality assurance program manager in Edgartown, MA is $138,874.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,600.00 and $170,000.00 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 job categories do people searching Quality Assurance Program Manager jobs in Edgartown, MA look for?

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

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

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

Quality Assurance Program Manager jobs near you
Infographic showing various Quality Assurance Program Manager job openings in Edgartown, MA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $138,874 per year, or $66.8 per hour.

Senior Associate, Supplier Quality

Tonix Pharmaceuticals

North Dartmouth, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Key responsibilities

  • Execute day-to-day operations of supplier quality assurance

  • Maintain the Approved Supplier List and supplier management files including audit documentation

  • Manage supplier quality agreement review and approval

Job description

Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti-Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X.
*Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication.
Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners.
Job Summary
The Senior Associate, Supplier Quality performs activities for the Quality Assurance Supplier Quality function. The individual in this position performs duties associated with the implementation and maintenance of Quality procedures, standards and systems related to GxP activities. The individual in this position executes aspects of the supplier quality management program that provides materials and services to Tonix for GxP operations as well as external contract organization activities.
The individual in this position works with the other Quality functions to ensure patient safety and compliance with FDA and other applicable global health authority requirements. The individual in this position also is directly involved in the execution of QA strategic planning for continuous improvement and reporting/escalation of quality issues and/or risk mitigation activities pertaining to GxP activities and to ensure a culture of quality and compliance.
Essential Functions
  • Execute day-to-day operations of supplier quality assurance
  • Maintain the Approved Supplier List and supplier management files including audit documentation
  • Execute GxP contractor and consultant qualification process
  • Manage supplier quality agreement review and approval
  • Maintain the Supplier Change Notification and Supplier Corrective Action Reporting processes to ensure supplier adherence to Tonix requirements
  • Provide compliance input for internal teams as well as external contract organizations related to supplier quality
  • Collect and monitor metrics to ensure control of systems and drive continuous improvements
  • Maintain and support the internal audit program as well as participate in regulatory inspections
  • Develop and implement GxP quality standards, policies, and procedures
  • Execute supplier audits with the supplier quality team, as needed.
  • Follow all established occupational health and safety procedures, good manufacturing practices (GMP's) and standard operating procedures (SOP's)
  • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork
  • Perform ad-hoc work/special projects as necessary to support Tonix on various business initiatives

Necessary Skills and Abilities
  • Demonstrated troubleshooting and problem-solving skills
  • Ability to analyze a wide variety of information and data to support decisions regarding potential risks associated with regulatory compliance
  • Knowledge of global pharmaceutical industry regulations, standards, and guidelines, such as, cGMPs (FDA, EMA), USP and other Pharmacopeia, FDA Guidance, 483s, Warning Letters, EIRs etc.
  • GxP auditing and inspection experience preferred
  • Collaborative, results-driven team player who excels in a dynamic environment
  • Dedicated team player who can withstand the high demands of a fast-paced environment
  • Strong planning and organizational skills
  • Comfortable working independently with minimal supervision
  • Highly organized, results driven, problem solver, and collaborator
  • Excellent organizational, written, and verbal communication skills
  • Demonstrated ability to perform the essential duties of the position with or without accommodation
  • Ability to travel up to 10%

Educational Requirements
  • Bachelor's degree in science or other related discipline or equivalent work experience required

Experience Requirements
  • Five (5) plus years of Supplier Quality related experience in the biotechnology/pharmaceutical industries required

Salary Range
$80,000-$110,000 USD
*Please note that Tonix does not offer sponsorship for this role.
Recruitment & Staffing Agencies
Tonix does not accept agency resumes unless contacted directly by internal Tonix Talent Acquisition. Please do not forward resumes to Tonix employees or any other company location; Tonix is not responsible for any fees related to unsolicited resumes.
Compensation & Benefits
Tonix provides a comprehensive compensation and benefits package which includes:
  • Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Accounts, Health Savings Account, and Employee Assistance Programs
  • Pet Insurance
  • Retirement Savings 401k with company match and annual discretionary stock options
  • Generous Paid Time Off, Sick Time, & Paid Holidays
  • Career Development and Training

Tonix provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, or any other characteristic protected by law. In addition to federal law requirements, Tonix complies with applicable state and local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfers, leaves of absence, compensation, and training. Tonix expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic, information, disability, veteran status, or any other characteristic protected by law.

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