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Senior Quality Assurance Engineer Jobs in Rochester, NH

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

QA Compliance Specialist - LSA Location: This position is based in our Portsmouth, NH office. The ... This role partners with Manufacturing, Quality Control, Validation, Engineering, and other ...

QA Compliance Specialist - LSA Location: This position is based in our Portsmouth, NH office. The ... This role partners with Manufacturing, Quality Control, Validation, Engineering, and other ...

QA Specialist II - Operations Location: Location: This position is based in our Portsmouth, NH ... Bachelor's degree in Life Sciences, Engineering, or a related field. A combination of education and ...

As a key member of the Quality Team, the Senior Supplier Quality Engineer will be to manage product ... Expertise applying statistical methods to quality assurance. * Ability to advise others on complex ...

QA Specialist II - Operations Location: Location: This position is based in our Portsmouth, NH ... Bachelor's degree in Life Sciences, Engineering, or a related field. A combination of education and ...

The role provides leadership for product quality assurance, manufacturing quality, supplier quality ... Bachelor's degree in Engineering, Quality, Life Sciences, Biomedical Engineering, or related ...

Senior Electrical Engineer

Portsmouth, NH · On-site

$150K - $170K/yr

Senior Electrical Engineer Job Location: Portsmouth, NH Role Description This is a full-time, on ... performing quality assurance on projects to maintain excellence in engineering solutions.

Showing results 41-60

Senior Quality Assurance Engineer information

See Rochester, NH salary details

$32

$55

$78

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:

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.

QA Specialist IV-Operations

Lonza

Portsmouth, NH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 11 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

QA Specialist IV-Operations
Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM-4:30 PM EST.
What you will get:
Below you will find a comprehensive summary of the benefits package we offer:
  • Performance-related bonus.
  • Medical, dental and vision insurance.
  • 401(k) matching plan.
  • Life insurance, as well as short-term and long-term disability insurance.
  • Employee assistance programs.
  • Paid time off (PTO).

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What will you do:
We are seeking a detail-oriented QA Specialist IV-Operations to support document review and quality oversight activities within a cGMP manufacturing environment. This role is responsible for reviewing and approving GMP documentation, ensuring compliance with internal procedures and regulatory requirements, and supporting cross-functional teams to maintain high-quality standards. The ideal candidate will bring strong technical writing and review experience, a solid understanding of quality systems, and the ability to work independently while collaborating effectively across the organization.
  • Independently review and approve GMP documentation, including SOPs, work instructions, forms, and electronic batch records within the document management system
  • Review and approve validation and qualification documentation, including protocols and summary reports for equipment, instrumentation, and computer systems
  • Review non-DMS documentation such as maintenance records, engineering documentation, and supporting quality records to ensure compliance
  • Provide detailed feedback and recommendations during document review to ensure accuracy, completeness, and adherence to procedures
  • Ensure document changes are appropriately justified, documented, and aligned with revision control processes
  • Serve as a subject matter resource for document review related to validation, equipment, and analytical systems
  • Collaborate with QA, Manufacturing, Engineering, and other stakeholders to resolve documentation and quality issues
  • Support continuous improvement efforts to enhance documentation practices, compliance, and overall quality systems

What we are looking for:
  • Bachelor's degree in scientific discipline or equivalent experience
  • 4-6 years of experience in a pharmaceutical, biotechnology, or cGMP-regulated environment
  • Strong experience reviewing and approving GMP documentation across operations, validation, engineering, or quality functions
  • Solid understanding of cGMP regulations, documentation practices, and quality systems
  • Strong attention to detail and analytical skills, with the ability to identify and resolve documentation and compliance issues
  • Effective written and verbal communication skills, with the ability to collaborate across cross-functional teams
  • Ability to manage multiple priorities and work independently while meeting deadlines
  • Customer-focused mindset with the ability to provide clear guidance and escalate issues as appropriate

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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