FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations ...
FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations ...
Program Manager
Taunton, MA · On-site
$58K/yr
Program Manager Pay Range: $ 58,700 Annually Schedule: 40 hrs.- Monday-Friday 8a-4p FLSA: Exempt ... Quality Assurance: Ensure the program delivers compassionate, individualized support that aligns ...
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Program Manager
Taunton, MA · On-site
$58K/yr
Program Manager Pay Range: $ 58,700 Annually Schedule: 40 hrs.- Monday-Friday 8a-4p FLSA: Exempt ... Quality Assurance: Ensure the program delivers compassionate, individualized support that aligns ...
Alert senior management of potential quality, compliance, supply, or safety risks. * Complete ... Drive operational improvement initiatives, programs, and projects. * Perform other tasks, as ...
New
Alert senior management of potential quality, compliance, supply, or safety risks. * Complete ... Drive operational improvement initiatives, programs, and projects. * Perform other tasks, as ...
New
Senior Salesforce QA Analyst
Providence, RI · On-site +1
$93K - $140K/yr
We offer health, dental, and vision insurance as well as programs that support your mental health ... Partner with release management and DevOps teams to support CI/CD validation, deployment ...
New
Senior Salesforce QA Analyst
Providence, RI · On-site +1
$93K - $140K/yr
We offer health, dental, and vision insurance as well as programs that support your mental health ... Partner with release management and DevOps teams to support CI/CD validation, deployment ...
New
Program Manager
Halifax, MA · On-site
$58K/yr
Program Manager Pay Range: $58,700 Annually Schedule: (40 hours) Monday-Friday 8:30a-4:30p FLSA ... Quality Assurance: Ensure the program delivers compassionate, individualized support that aligns ...
Quick apply
Program Manager
Halifax, MA · On-site
$58K/yr
Program Manager Pay Range: $58,700 Annually Schedule: (40 hours) Monday-Friday 8:30a-4:30p FLSA ... Quality Assurance: Ensure the program delivers compassionate, individualized support that aligns ...
Program Manager
Acushnet, MA · On-site
$58K/yr
Program Manager Pay Range: $58,700 Annually Schedule: (40 hours) Monday-Friday 8:00a-4:00p FLSA ... Quality Assurance: Ensure the program delivers compassionate, individualized support that aligns ...
New
Quick apply
Program Manager
Acushnet, MA · On-site
$58K/yr
Program Manager Pay Range: $58,700 Annually Schedule: (40 hours) Monday-Friday 8:00a-4:00p FLSA ... Quality Assurance: Ensure the program delivers compassionate, individualized support that aligns ...
New
Manage a team of Quality Assurance Documentation Specialists and ensure successful training and ... Prepare nuclear specialty valve documentation packages in accordance with the invoked QA Program ...
Manage a team of Quality Assurance Documentation Specialists and ensure successful training and ... Prepare nuclear specialty valve documentation packages in accordance with the invoked QA Program ...
Quality Documentation Supervisor
Mansfield, MA · On-site
$90K/yr
Manage a team of Quality Assurance Documentation Specialists and ensure successful training and ... Prepare nuclear specialty valve documentation packages in accordance with the invoked QA Program ...
Quality Documentation Supervisor
Mansfield, MA · On-site
$90K/yr
Manage a team of Quality Assurance Documentation Specialists and ensure successful training and ... Prepare nuclear specialty valve documentation packages in accordance with the invoked QA Program ...
Manage a team of Quality Assurance Documentation Specialists and ensure successful training and ... Prepare nuclear specialty valve documentation packages in accordance with the invoked QA Program ...
Manage a team of Quality Assurance Documentation Specialists and ensure successful training and ... Prepare nuclear specialty valve documentation packages in accordance with the invoked QA Program ...
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 1st Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 1st Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 3rd Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 3rd Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 1st Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 1st Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 3rd Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 2nd Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 2nd Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 3rd Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 3rd Shift
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 2nd Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector I - 2nd Shift
Fall River, MA · On-site
$23 - $30/hr
Quality Assurance Manager Salary Range : $23 - $30 PURPOSE The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the ...
QA Inspector II - 2nd Shift
$26 - $33/hr
Quality Control Manager Salary Range:$26 - $33 Job Purpose: The purpose of the QA Inspector position is to monitor and ensure shop floor activities and ensure product quality is maintained throughout ...
QA Inspector II - 2nd Shift
$26 - $33/hr
Quality Control Manager Salary Range:$26 - $33 Job Purpose: The purpose of the QA Inspector position is to monitor and ensure shop floor activities and ensure product quality is maintained throughout ...
Quality Control Manager Salary Range:$26 - $33 Job Purpose: The purpose of the QA Inspector position is to monitor and ensure shop floor activities and ensure product quality is maintained throughout ...
Quality Control Manager Salary Range:$26 - $33 Job Purpose: The purpose of the QA Inspector position is to monitor and ensure shop floor activities and ensure product quality is maintained throughout ...
Quality Manager
Lincoln, RI · On-site
Develops and implements, as necessary, Quality Assurance and Continual Improvement programs to ... Manages and directs required testing throughout all processes. * Provides analyzed data reports as ...
Quality Manager
Lincoln, RI · On-site
Develops and implements, as necessary, Quality Assurance and Continual Improvement programs to ... Manages and directs required testing throughout all processes. * Provides analyzed data reports as ...
Qa Program Manager information
See Fall River, MA salary details
$24.1K - $36.3K
12% of jobs
$44.4K is the 25th percentile. Wages below this are outliers.
$36.3K - $48.5K
20% of jobs
$48.5K - $60.8K
14% of jobs
The median wage is $64.9K / yr.
$60.8K - $73K
13% of jobs
$73K - $85.2K
9% of jobs
$85.2K - $97.5K
5% of jobs
$105.1K is the 75th percentile. Wages above this are outliers.
$97.5K - $109.7K
4% of jobs
$109.7K - $121.9K
4% of jobs
$121.9K - $134.1K
2% of jobs
$134.1K - $146.4K
0% of jobs
$146.4K - $158.6K
17% of jobs
$24.1K
$86.5K
$158.6K
How much do qa program manager jobs pay per year?
As of Aug 14, 2026, the average yearly pay for qa program manager in Fall River, MA is $86,490.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,200.00 and $136,500.00 per year, depending on experience, location, and employer.
What is a QA program manager?
A QA Program Manager is a professional responsible for overseeing and coordinating quality assurance (QA) programs within an organization. They manage teams, set QA standards, and ensure that products or services meet quality requirements before they are released to customers. Their role often includes strategic planning, process improvement, risk management, and collaborating with other departments to maintain high-quality deliverables. QA Program Managers also monitor performance metrics, facilitate audits, and drive continuous improvement initiatives.
What is the difference between Qa Program Manager vs Qa Analyst?
| Aspect | Qa Program Manager | Qa Analyst |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in quality assurance, engineering, or related field; certifications like ASQ CQE or CQA are common | Usually holds a bachelor's degree in quality assurance, engineering, or related area; certifications like ISTQB or ASQ CQA are beneficial |
| Work Environment | Oversees multiple projects, manages teams, and develops quality programs within organizations | Performs testing, inspections, and analysis to identify quality issues; works closely with development teams |
| Employer & Industry Usage | Used in manufacturing, software, and engineering sectors to lead quality initiatives | Commonly found in software, manufacturing, and healthcare industries for testing and analysis |
The Qa Program Manager focuses on developing and managing quality programs across projects, while the Qa Analyst concentrates on executing testing and quality assessments. Both roles require relevant certifications and work within similar industries, but their responsibilities differ in scope and leadership level.
What are the key skills and qualifications needed to thrive as a QA program manager?
To thrive as a QA Program Manager, you need a solid background in quality assurance methodologies, project management, and a relevant degree such as in computer science or engineering. Familiarity with QA automation tools, test management systems, and certifications like PMP or ISTQB are typically required. Strong leadership, communication, and problem-solving skills help you effectively manage teams and collaborate across departments. These abilities are crucial for ensuring software quality, meeting project deadlines, and aligning QA initiatives with organizational goals.
Is a QA Program Manager a stressful job?
A QA Program Manager role can be stressful due to the responsibility of ensuring product quality, meeting deadlines, and coordinating across teams. The job often involves managing multiple projects, troubleshooting issues, and maintaining high standards, which can contribute to work-related stress. However, stress levels vary depending on organizational culture, workload, and individual skills in project management and communication.
What are some common challenges faced by QA program managers when coordinating cross-functional testing efforts?
QA Program Managers often encounter challenges such as aligning testing schedules across multiple teams, ensuring consistent communication between development, QA, and product stakeholders, and managing shifting priorities or resource constraints. Successfully navigating these issues typically requires strong organizational skills, proactive risk management, and the ability to foster collaboration among diverse groups. Implementing clear processes and regular status updates can help minimize misunderstandings and keep testing efforts on track.
What job categories do people searching Qa Program Manager jobs in Fall River, MA look for?
The top searched job categories for Qa Program Manager jobs in Fall River, MA are:
What cities near Fall River, MA are hiring for Qa Program Manager jobs?
Cities near Fall River, MA with the most Qa Program Manager job openings:
Full-time
Re-posted 22 days ago
Job description
SUMMARY/OBJECTIVE
This position supports activities of the Quality Assurance Department regarding pharmaceutical manufacturing, testing and packaging to ensure compliance with all relevant pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations, investigations and CAPA. Adheres to Client compliance initiatives, including
following all quality and division/company policy requirements. Helps to ensure that all Client products meet quality requirements by supporting all assigned quality aspects of product approval. The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards are maintained and product integrity is preserved.
RESPONSIBILITIES
1. Provide support to GMP investigations, validation documentation review and approval, identify gaps within existing Quality Systems and propose solutions for functional management;
2. Participates/leads internal/external audits, prepare and issue audit reports. Recommend remediation actions and follow up on implementation of the plan.
3. Supports resolution of technical and compliance issues/gap analysis.
4. Aides implementation of Quality Systems/System Improvements.
5. Supports and assists with Quality systems-related training, including compliance with cGMP and SOPs.
6. Interface with key quality, manufacturing, customers and coordinate documentation impacting quality areas.
7. Review/approval of all cGMP documents generated across site to include (but not limited to): SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control, deviation & document revisions, etc.
8. Participates in activities associated with primary batch record review, non-conformances investigation and CAPA.
9. Work in coordination with regulatory affairs group in support of ANDA submissions.
10. Provides QA review/approval of all cGMP documents associated with manufacture of product.
11. Communicates with contractors and internal manufacturing/technical groups regarding compliance and quality issues (i.e., batch documentation, investigations, timelines and data related issues).
12. Authors or revises SOPs as necessary.
13. Actively engaged in the training of staff with lesser experience or knowledge of quality assurance processes. Educate and instruct QA and plant personnel in quality best practices for sampling, labeling,
good documentation practices, equipment sanitation. Confirm these procedures are being adhered to, taking corrective actions when non-conformances are observed.
14. Routinely provide input to quality and operations management for better operational procedures to improve overall efficiency and regulatory compliance.
15. Assist in development of special department projects and work in conjunction with quality management.
16. Other duties as assigned.
COMPETENCIES
1. Project Management
2. Technical Capacity.
3. Discretion.
4. Problem Solving/Analysis.
5. Decision Making.
6. Communication Proficiency.
7. Collaboration Skills.
8. Learning Agility
9. Managing Changing Priorities
POSITION TYPE/EXPECTED HOURS OF WORK
This is a full-time position requiring 40 or more hours of work per week.
This position supports activities of the Quality Assurance Department regarding pharmaceutical manufacturing, testing and packaging to ensure compliance with all relevant pharmaceutical regulatory requirements: FDA, GMP. Provides QA oversight to operations under direction of the QA Manager. Provides review, impact/risk assessment analysis, detailed improvement plans for change controls, deviations, investigations and CAPA. Adheres to Client compliance initiatives, including
following all quality and division/company policy requirements. Helps to ensure that all Client products meet quality requirements by supporting all assigned quality aspects of product approval. The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards are maintained and product integrity is preserved.
RESPONSIBILITIES
1. Provide support to GMP investigations, validation documentation review and approval, identify gaps within existing Quality Systems and propose solutions for functional management;
2. Participates/leads internal/external audits, prepare and issue audit reports. Recommend remediation actions and follow up on implementation of the plan.
3. Supports resolution of technical and compliance issues/gap analysis.
4. Aides implementation of Quality Systems/System Improvements.
5. Supports and assists with Quality systems-related training, including compliance with cGMP and SOPs.
6. Interface with key quality, manufacturing, customers and coordinate documentation impacting quality areas.
7. Review/approval of all cGMP documents generated across site to include (but not limited to): SOPs, technical reports, validation documents, QA assessment, APRs, audit documents, change control, deviation & document revisions, etc.
8. Participates in activities associated with primary batch record review, non-conformances investigation and CAPA.
9. Work in coordination with regulatory affairs group in support of ANDA submissions.
10. Provides QA review/approval of all cGMP documents associated with manufacture of product.
11. Communicates with contractors and internal manufacturing/technical groups regarding compliance and quality issues (i.e., batch documentation, investigations, timelines and data related issues).
12. Authors or revises SOPs as necessary.
13. Actively engaged in the training of staff with lesser experience or knowledge of quality assurance processes. Educate and instruct QA and plant personnel in quality best practices for sampling, labeling,
good documentation practices, equipment sanitation. Confirm these procedures are being adhered to, taking corrective actions when non-conformances are observed.
14. Routinely provide input to quality and operations management for better operational procedures to improve overall efficiency and regulatory compliance.
15. Assist in development of special department projects and work in conjunction with quality management.
16. Other duties as assigned.
COMPETENCIES
1. Project Management
2. Technical Capacity.
3. Discretion.
4. Problem Solving/Analysis.
5. Decision Making.
6. Communication Proficiency.
7. Collaboration Skills.
8. Learning Agility
9. Managing Changing Priorities
POSITION TYPE/EXPECTED HOURS OF WORK
This is a full-time position requiring 40 or more hours of work per week.
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008