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Senior Qa Associate Jobs in Worcester, MA (NOW HIRING)

RoslinCT US

Sr. QA Training Specialist

Hopkinton, MA

$90K - $124K/yr

ACCELERATING YOUR FUTURE The Sr. Training Specialist is position responsible for supporting the ... Complete other responsibilities, as assigned within the Quality Assurance department. * Serve as a ...

Dyne Tx

Associate Director, GMP QA Operations

Waltham, MA · On-site

$160 - $195/hr

Role Summary The Associate Director, QA Operations serves as the QA technical lead for external manufacturing and testing project teams, ensuring the effective development, implementation, and ...

Nova Biomedical

Senior Quality Director

Waltham, MA · Hybrid

The Sr. Director, Quality will provide direct oversight of CAPA management, ISO/QSR employee ... Bachelors degree in the sciences or another technical discipline, or 10+ years of quality assurance ...

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Senior Qa Associate information

See Worcester, MA salary details

$28.9K

$74K

$132.7K

How much do senior qa associate jobs pay per year?

As of Sep 3, 2026, the average yearly pay for senior qa associate in Worcester, MA is $74,036.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,400.00 and $94,800.00 per year, depending on experience, location, and employer.

What does a Senior QA Associate do?

A Senior QA (Quality Assurance) Associate is responsible for overseeing and executing quality control processes to ensure that products or services meet established standards and regulatory requirements. They design and implement test plans, conduct inspections, analyze data, and collaborate with cross-functional teams to identify and resolve quality issues. Additionally, Senior QA Associates often mentor junior team members and help improve overall quality systems and procedures within an organization.

What are the key skills and qualifications needed to thrive as a Senior QA Associate?

To thrive as a Senior QA Associate, you need a solid background in quality assurance methodologies, process validation, and regulatory compliance, typically supported by a relevant degree and several years of industry experience. Familiarity with quality management systems (QMS), electronic documentation tools, and regulatory standards like GMP or ISO is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These competencies are crucial to ensure product quality, regulatory adherence, and continuous process improvement in highly regulated environments.

What are some typical challenges faced by Senior QA Associates when managing multiple testing projects simultaneously?

Senior QA Associates often juggle several testing projects at once, which requires excellent organizational and prioritization skills. Common challenges include balancing tight deadlines, ensuring thorough test coverage, and coordinating with cross-functional teams such as development, product management, and regulatory affairs. Proactively communicating and setting clear expectations with stakeholders is key to managing these challenges. Additionally, Senior QA Associates often mentor junior team members, adding another layer of responsibility to their role.

What is the difference between Senior Qa Associate vs Quality Assurance Tester?

AspectSenior Qa AssociateQuality Assurance Tester
Required CredentialsBachelor's degree in Computer Science or related field; experience in QAHigh school diploma or equivalent; some technical training or certifications preferred
Work EnvironmentCollaborates with cross-functional teams; involved in planning and oversightPrimarily executes test cases; reports bugs and issues
Employer & Industry UsageUsed in software development, technology companies, and IT servicesCommon in software firms, startups, and quality-focused organizations
Search & Comparison IntentOften compared for experience level and responsibilitiesCompared for entry-level or mid-level QA roles

The Senior Qa Associate typically has more experience, responsibilities in planning, and oversight in quality assurance processes, whereas a Quality Assurance Tester focuses on executing tests and identifying bugs. The senior role often involves collaboration with development teams and strategic planning, making it suitable for professionals with more experience in QA.

What are the most commonly searched types of Senior Qa jobs in Worcester, MA?

The most popular types of Senior Qa jobs in Worcester, MA are:

What cities near Worcester, MA are hiring for Senior Qa Associate jobs?

Cities near Worcester, MA with the most Senior Qa Associate job openings:

Senior Qa Associate jobs near you
Infographic showing various Senior Qa Associate job openings in Worcester, MA as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $74,036 per year, or $35.6 per hour.

Senior Quality Assurance Document Specialist

Candel Therapeutics

Needham, MA • On-site

$143K - $155K/yr

Full-time

Re-posted 8 days ago

Job description

  • Location:Hybrid, Needham, MA
  • Salary: $143k-$155k
Why Work With Us?
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.
Our Science: Advancing Cancer Immunotherapies
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it's an exciting time to join us and help bring transformative cancer treatments to patients. Learn more:www.candeltx.com
Position Summary:
Cross-functional to support relevant Quality Systems GXP activities in adherence to applicable regulations (FDA, EU, etc.) and standards (ICH Q10, ISO). Also supports the implementation and improvement of Quality Systems to ensure quality and adherence with current Good Manufacturing Practice (cGMP) and inspection readiness.
Essential Areas of Responsibility:
  • Administers Document Management Program and provides support to end users for the creation, revision, and retirement of documents including:
  • Reviews GxP documents and records for completeness and compliance with internal procedures and applicable regulations and ensures ALCOA++ principles are followed to ensure data robustness.
  • Supports and manages document lifecycle in the Electronic Quality Management System (eQMS)
  • Maintains and improves Document Management Program procedures
  • Provides training on the Document Management Program
  • Acts as Administrator for Document Management within the eQMS
  • Manages physical document archival and retention program
  • Administers the Training Management Program and provides support to end users for the maintenance of training activities including:
  • Maintains user roles, training curricula, and training assignments.
  • Maintains and improves Training Management Program procedures
  • Provides training on the Training Management Program, as well as Employee Onboarding Program related policies and procedures.
  • Assists document owners in generating training materials and quiz questions
  • Acts as Administrator for Training Management within the eQMS
  • Additional duties to include:
  • Inspection readiness and execution tasks, as assigned
  • Internal audit support
  • Deviation, CAPA, Change Control, and Supplier Qualification support
  • Preparation of Quality Management System metrics
  • eQMS, design and validation support
  • Continuous Improvement initiatives
  • Other responsibilities as assigned by management
Education, Experience and Skill Requirements:
Education:
  • BS/BA in a scientific or engineering discipline with 6+ years of experience in pharmaceutical/ biotech industry within Quality Assurance or Quality (Assurance) exposure, or equivalent experiences
  • Or, Associate's degree in a scientific or engineering discipline with 8+ years of Quality experience or Quality (Assurance) exposure or equivalent experiences
Experience:
  • Knowledge in 21 CFR Part 11, Annex 11, CFR 210, CFR 211, GxP practices
  • Knowledge of current regulatory and industry guidelines
  • Exposure to global health agency regulations
  • Internal audit/self-inspection experience
  • Experience in electronic Quality Management Systems
  • Proficient in Microsoft Office suite (Word, Excel, PowerPoint, Outlook, and Teams)
  • Familiar with SmartSheet and SharePoint platforms
  • Excellent written and oral communication skills
  • Strong organizational skills with the ability to effectively prioritize and manage multiple projects and tasks with attention to detail in a rapidly changing environment
  • Ability to proactively resolve issues in a diplomatic, flexible, and constructive manner
  • Highly motivated, ethical individual with excellent time management skills
  • Skilled at building consensus, securing stakeholder buy-in, and advancing strategic priorities in a matrixed organization
Must be authorized to work in US. We cannot provide sponsorships.
*** NOTE: We are not accepting resumes from agencies. ***

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