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Quality Assurance Program Manager Jobs in Worcester, MA

Ardelyx

Quality Assurance Manager

Waltham, MA · Hybrid

The Quality Assurance Manager will serve within Quality Assurance, providing oversight and hands-on support for achieving QA milestones, in a fast-paced pharmaceutical environment. This role will be ...

Ardelyx

Quality Assurance Manager

Waltham, MA · Hybrid

$139K - $169K/yr

The Quality Assurance Manager will serve within Quality Assurance, providing oversight and hands-on support for achieving QA milestones, in a fast-paced pharmaceutical environment. This role will be ...

Ardelyx

Quality Assurance Manager

Waltham, MA · On-site

$139K - $169K/yr

The Quality Assurance Manager will serve within Quality Assurance, providing oversight and hands-on support for achieving QA milestones, in a fast-paced pharmaceutical environment. This role will be ...

Ardelyx

Quality Assurance Manager

Waltham, MA · Hybrid

$139K - $169K/yr

The Quality Assurance Manager will serve within Quality Assurance, providing oversight and hands-on support for achieving QA milestones, in a fast-paced pharmaceutical environment. This role will be ...

Cesna Group

QA Supervisor

Ayer, MA · On-site

$50K - $100K/yr

Responsible for coordination, implementation, and maintenance of QA Program. * Supervise daily QC Technician Activities. * Responsible for identifying quality and food safety issues & verify they ...

SofTec Solutions

QA Analyst

Waltham, MA · On-site

... of program logic and system flow. • Manages and participates in the analysis and design phases of QA projects by collaborating with off shore team to create test scenario and acceptance test ...

Abbott

Supervisor Quality Assurance

Westford, MA · On-site

Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an ... Support all Company initiatives as identified by management and in support of Quality Management ...

Collabera

QA Analyst

Waltham, MA · On-site

... Vendor Management Programs. Collabera recognizes true potential of human capital and provides ... Title: QA Lead Location: Waltham, MA Duration: 6 month (may extend) Our top direct client is ...

Abbott

Supervisor Quality Assurance

Westford, MA

Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an ... Support all Company initiatives as identified by management and in support of Quality Management ...

Abbott

Supervisor Quality Assurance

Westford, MA · On-site

Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an ... Support all Company initiatives as identified by management and in support of Quality Management ...

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

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 Aug 11, 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 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.

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 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:
Quality Assurance Program Manager jobs near you
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.

Quality Assurance Manager

Ardelyx

Waltham, MA • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 15 days ago

Job description

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients.
 
Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive.
 
We foster an inclusive environment where employees are respected, supported, and empowered to make an impact — both within our company and in the lives of patients we serve.
 
Position Summary:
 
The Quality Assurance Manager will serve within Quality Assurance, providing oversight and hands-on support for achieving QA milestones, in a fast-paced pharmaceutical environment. This role will be deeply engaged in day-to-day quality operations, including batch record review, product disposition, investigations, quality agreements, and quality systems support.
 
The position requires strong technical expertise in GMP quality systems, CMC QA, and quality risk management, along with the ability to independently manage complex quality activities and partner cross-functionally across the organization. In addition to core operational responsibilities, this individual will serve as the primary QA representative supporting operations on the East Coast and provide occasional back-up support to department management to help ensure continuity when coverage is needed.
 
Responsibilities:
  • Serve as the primary QA representative supporting day-to-day activities for teams and operations located on the east coast
  • Provide QA oversight for CMC activities supporting development, clinical, and commercial products
  • Evaluate completed manufacturing documentation (batch records, COAs, packaging records, and related GMP documentation) from CMOs to ensure accuracy, completeness, and compliance
  • Review and approve batch record and product disposition activities in support of clinical trials, process validation, registration activities, and commercial product distribution
  • Review and approve development, qualification, and validation protocols and reports
  • Collaborate cross-functionally with CMC, Regulatory Affairs, Supply Chain, and external partners to support quality and compliance activities throughout the product lifecycle
  • Provide QA oversight of CMO and suppliers’ activities to ensure required quality standards and regulatory expectations are maintained
  • Generate Annual Product Quality Report, quality metrics, management review inputs, and KPI reporting
  • Ensure Quality Agreements clearly define GMP responsibilities, and quality oversight expectations and responsibilities between parties
  • Assist with inspection readiness activities and support internal and external GMP audits
  • Participate in quality systems activities, including deviations, investigations, OOS events, change controls, and related GMP processes
  • Identify and support continuous improvement opportunities within QA processes and systems
  • Ensure compliance with cGMP, ICH, FDA, EU, and other applicable regulatory requirements
 
This is a hybrid role (2-3 days in office) at our Waltham, MA headquarters.
 
Qualifications:
  • Bachelor’s degree in science or related field with 10+ years of progressive GxP Quality Assurance experience within biotechnology or equivalent experience.
  • Experience in relevant CMC area (DS, DP), with an ability to introduce Quality-relevant (phase appropriate) best practices into the CMC development processes
  • Experience in a manufacturing setting as a Quality person in the plant (QA PIP)
  • Extensive knowledge of GMP regulations and guidance (such as FDA, EU, and ICH)
  • Experience with Quality Assurance systems and processes
  • Excellent investigational and QA problem-solving skills
  • Strong technical writing skills
  • Advanced software skills including SharePoint, and Veeva
The anticipated annualized base pay range for this full-time position is $139,000 - $169,000 Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.
 
Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.
 
Ardelyx is an equal opportunity employer.
 
We do not accept unsolicited resumes from search firms, or recruiters or similar vendors. Any such unsolicited resume submitted to any employee or through Company's career site without a valid, signed search agreement signed by Company's authorized representative will be deemed the property of the company, and no fees will be paid in the event of a hire. Company will have the right to hire any such candidate at its discretion without any financial obligation or fee owed to the vendor. Any verbal or written communication with a Company employee outside of this process will not be considered a binding agreement.