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Senior Quality Assurance Engineer Jobs in Rochester, NH

Lonza

Quality Assurance Manager, Operations

Portsmouth, NH · On-site

$100 - $120/hr

United States, Portsmouth (New Hampshire) Quality Assurance Manager, Operations Location: This ... Partner cross-functionally with Manufacturing, MSAT, Engineering, QC, Validation, and Supply Chain ...

Lonza

Associate Director, QA Ops

Portsmouth, NH

Associate Director, QA Ops Location: This position is based in our Portsmouth, NH office. The ... Partner with cross-functional teams (Manufacturing, MSAT, Engineering, QC, Validation, and Supply ...

Lonza

Associate Director, QA Ops

Portsmouth, NH · On-site

Associate Director, QA Ops Location: This position is based in our Portsmouth, NH office. The ... Partner with cross-functional teams (Manufacturing, MSAT, Engineering, QC, Validation, and Supply ...

A/Z Corp

Quality Assurance/Control Manager

Kittery, ME · On-site

Support updates to formal Corporate QA/QC Program Standard Operating Procedure (SOP); * Support ... Support the development and formalization of the corporate Project Engineering / Manager Training ...

Lonza

QA Specialist IV-Operations

Portsmouth, NH · On-site

Collaborate with QA, Manufacturing, Engineering, and other stakeholders to resolve documentation ... and quality issues * Support continuous improvement efforts to enhance documentation practices ...

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Senior Quality Assurance Engineer information

See Rochester, NH salary details

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$55

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How much do senior quality assurance engineer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for senior quality assurance engineer in Rochester, NH is $55.52, according to ZipRecruiter salary data. Most workers in this role earn between $47.16 and $63.17 per hour, depending on experience, location, and employer.

What is a senior quality assurance engineer?

Senior Quality Assurance Engineers are experienced professionals responsible for overseeing and improving the quality of software products. They develop and execute test plans, identify defects, and ensure that products meet specified requirements before release. In addition to hands-on testing, they often mentor junior QA staff, refine testing processes, and collaborate closely with developers and product managers to drive quality initiatives. Their role is vital in delivering reliable, high-performing software to users.

How does a senior quality assurance engineer typically collaborate with cross-functional teams during a software development project?

A Senior Quality Assurance Engineer works closely with developers, product managers, and sometimes UX/UI designers throughout the software development lifecycle. They participate in planning meetings to understand requirements, provide input on testability, and help define acceptance criteria. Regular collaboration ensures that any issues are identified early, and quality standards are maintained. Additionally, they may lead defect triage meetings and mentor junior QA staff, fostering a culture of continuous improvement across teams.

What are the key skills and qualifications needed to thrive as a senior quality assurance engineer, and why are they important?

To thrive as a Senior Quality Assurance Engineer, you need deep expertise in software testing methodologies, test automation, and a strong understanding of software development lifecycles, usually supported by a degree in computer science or a related field. Familiarity with automated testing tools such as Selenium, JUnit, or TestNG, as well as experience with CI/CD platforms, is typically required, and certifications like ISTQB can be advantageous. Outstanding analytical skills, attention to detail, and effective communication enable you to identify, document, and relay complex issues efficiently within cross-functional teams. These skills and qualities are crucial to ensuring software reliability, reducing defects, and accelerating high-quality product releases.

What is the difference between Senior Quality Assurance Engineer vs Quality Assurance Analyst?

AspectSenior Quality Assurance EngineerQuality Assurance Analyst
CredentialsBachelor's in Computer Science or related field, certifications like ISTQBBachelor's in IT, Computer Science, or related field, ISTQB certification often preferred
Work EnvironmentLead testing efforts, develop testing strategies, mentor junior staffExecute test cases, report bugs, perform manual and automated testing
Industry UsageUsed across software development, tech, and IT companiesCommon in software, finance, healthcare, and tech sectors

The main difference is that Senior Quality Assurance Engineers typically lead testing projects, develop strategies, and mentor teams, while Quality Assurance Analysts focus on executing tests and reporting issues. Both roles require similar credentials and are vital in software quality assurance across industries.

Is a senior quality assurance engineer a good career?

A senior quality assurance engineer is a valuable role in software development, focusing on testing, process improvement, and ensuring product quality. It offers opportunities for career growth, specialization in testing tools and methodologies, and often requires strong analytical and communication skills. The role is generally considered stable and in demand across various industries that develop software or hardware products.

What cities near Rochester, NH are hiring for Senior Quality Assurance Engineer jobs?

Cities near Rochester, NH with the most Senior Quality Assurance Engineer job openings:

Senior Quality Assurance Engineer jobs near you
Infographic showing various Senior Quality Assurance Engineer job openings in Rochester, NH as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $115,231 per year, or $55.4 per hour.

Quality Assurance (QA) Roles (Entry to Mid-Level) (Day-Shift)

Lonza

Portsmouth, NH • On-site

Full-time

Posted 18 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

We're Hiring: Quality Assurance (QA) Professionals - Multiple Levels & Areas
Join our team and grow your career in Quality! We have exciting QA opportunities across multiple functions and levels, supporting both Cell Therapy and Biologics operations.
Job Summary - Quality Assurance (QA) Roles (Entry to Mid-Level)
The Quality Assurance (QA) function is responsible for ensuring that all products, processes, and systems comply with internal standards, regulatory requirements, and industry best practices. QA professionals support quality and compliance activities across manufacturing, laboratory, and operational environments, with responsibilities that may include compliance oversight, deviation management, investigations, batch record review, on-the-floor quality support, and project or program management.
At the entry level, QA professionals focus on executing routine quality tasks such as reviewing documentation, supporting Good Manufacturing Practice (GMP) compliance, assisting with investigations, and ensuring adherence to Standard Operating Procedures (SOPs). As experience grows, individuals take on increased ownership in deviation investigations, CAPA management, audit readiness, and cross-functional collaboration.
Mid-level QA professionals are expected to lead complex investigations, manage quality systems, support regulatory inspections, and drive continuous improvement initiatives. They may also oversee quality-related projects or programs, partner with manufacturing and technical teams, and provide guidance to junior staff. Roles such as QA Project Manager and QA Program Manager involve coordinating cross-functional efforts, managing timelines, mitigating risks, and ensuring successful delivery of quality and compliance objectives.
Across all levels, QA team members play a critical role in maintaining product quality, ensuring patient safety, and supporting regulatory compliance in a fast-paced, highly regulated environment.
Key Responsibilities (may vary by role and level):
  • Ensure compliance with GMP, regulatory requirements, and internal quality standards
  • Review and approve batch records, protocols, reports, and quality documentation
  • Support and/or lead deviation investigations, root cause analysis, and CAPA implementation
  • Provide on-the-floor QA support to manufacturing and operations teams
  • Participate in audits and inspections (internal, client, and regulatory)
  • Monitor quality metrics and identify opportunities for continuous improvement
  • Support change controls, risk assessments, and validation activities
  • Collaborate cross-functionally with Manufacturing, QC, Regulatory, and Engineering teams
  • Lead or support quality-related projects and programs, including timeline and risk management

Basic Qualifications (Entry-Level):
  • Bachelor's degree in Life Sciences, Engineering, or related field (or equivalent experience)- A combination of education and years of experience will be considered.
  • Strong attention to detail and organizational skills
  • Basic understanding of GMP or regulated environments preferred
  • Ability to follow SOPs and accurately document work
  • Strong communication and willingness to learn

Preferred Qualifications (Mid-Level):
  • 3-7+ years of experience in QA within a GMP-regulated industry
  • Hands-on experience with deviations, investigations, CAPAs, and change controls
  • Experience with batch record review and quality systems
  • Familiarity with audits and regulatory inspections
  • Experience with systems such as TrackWise, Veeva, LIMS, or similar

Key Skills and Competencies:
  • Strong knowledge of GMP and quality systems
  • Critical thinking and problem-solving skills
  • Attention to detail and data integrity mindset
  • Effective communication and cross-functional collaboration
  • Ability to manage multiple priorities and meet deadlines
  • Decision-making and risk assessment capabilities
  • Project management skills (for mid-level and above roles)
  • Continuous improvement mindset

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

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