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Software Quality Operations Associate Jobs in Exeter, NH

Strategic Operations Associate II Location: Portsmouth, NH, (On-site) As a Strategic Operations ... Working closely with Manufacturing, MSAT, Quality, Engineering, Validation, and Project Management ...

Quality Engineer

Manchester, NH · On-site

$71K - $92K/yr

This position will support manufacturing quality operations in a dynamic, fast-paced, medical ... Microsoft Office software (Word, Outlook, Excel). QUALIFICATIONS AND SKILLS: * 3 + years of ...

Quality Engineer

Manchester, NH · On-site

$71K - $92K/yr

This position will support manufacturing quality operations in a dynamic, fast-paced, medical ... Microsoft Office software (Word, Outlook, Excel). QUALIFICATIONS AND SKILLS: * 3 + years of ...

QA Engineer Technician

Derry, NH · On-site

$70K - $80K/yr

Key Responsibilities Quality Assurance / Production Test / Operations * Test, troubleshoot, and ... Associates degree in Electronics and a minimum of 2 years of related experience. * Self-motivated ...

QA Engineer Technician

Derry, NH · On-site

$70K - $80K/yr

Key Responsibilities Quality Assurance / Production Test / Operations * Test, troubleshoot, and ... Associates degree in Electronics and a minimum of 2 years of related experience. * Self-motivated ...

Showing results 21-40

Software Quality Operations Associate information

See Exeter, NH salary details

$11

$27

$51

How much do software quality operations associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for software quality operations associate in Exeter, NH is $27.40, according to ZipRecruiter salary data. Most workers in this role earn between $18.61 and $32.02 per hour, depending on experience, location, and employer.

What is a software quality operations associate?

A Software Quality Operations Associate is a professional who supports the quality assurance (QA) processes within a software development organization. Their main responsibilities include monitoring software quality, helping to implement QA procedures, coordinating testing activities, and ensuring that software products meet established standards before release. They often work closely with QA engineers, developers, and product managers to track defects, document issues, and improve workflow efficiency. This role is essential for maintaining high software quality and facilitating smooth operations within the QA team.

What are some of the typical challenges faced by a software quality operations associate when coordinating between development and QA teams?

One of the main challenges for a Software Quality Operations Associate is ensuring clear and timely communication between development and QA teams, especially when managing tight release schedules. Balancing the need for rapid deployment with thorough testing can create pressure to prioritize tasks and manage resources efficiently. Additionally, adapting to shifting project requirements and quickly resolving bugs or discrepancies requires strong organizational and problem-solving skills. Proactively fostering collaboration and maintaining detailed documentation help overcome these obstacles and contribute to smoother software delivery.

What are the key skills and qualifications needed to thrive as a software quality operations associate, and why are they important?

To thrive as a Software Quality Operations Associate, you need a solid understanding of software development processes, quality assurance principles, and a relevant degree in computer science or a related field. Familiarity with test management tools (like JIRA or TestRail), bug tracking systems, and automation frameworks is typically required, along with any relevant QA certifications. Strong analytical thinking, attention to detail, and effective communication skills help you excel in identifying issues and collaborating with development teams. These skills ensure the delivery of high-quality software products and support efficient, error-free operations.

What is the difference between Software Quality Operations Associate vs Software Quality Analyst?

AspectSoftware Quality Operations AssociateSoftware Quality Analyst
CredentialsTypically requires a bachelor's degree in computer science, quality assurance, or related fieldUsually requires a bachelor's degree in computer science, software engineering, or related discipline
Work EnvironmentWorks within software development teams, focusing on process and operationsFocuses on testing, identifying bugs, and analyzing software quality
Employer & Industry UsageCommon in tech companies, software firms, and IT departmentsWidely used in software development, IT, and quality assurance sectors

The Software Quality Operations Associate primarily handles quality processes and operational tasks within software teams, while the Software Quality Analyst concentrates on testing and analyzing software quality. Both roles require similar educational backgrounds and are integral to software development, but they focus on different aspects of quality assurance.

What job categories do people searching Software Quality Operations Associate jobs in Exeter, NH look for?

The top searched job categories for Software Quality Operations Associate jobs in Exeter, NH are:

Infographic showing various Software Quality Operations Associate job openings in Exeter, NH as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $56,999 per year, or $27.4 per hour.

Strategic Operation Associate II

Lonza

Portsmouth, NH • On-site

Full-time

Medical, Dental, Vision

Posted 16 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

Job Title: Strategic Operations Associate II
Location: Portsmouth, NH, (On-site)
As a Strategic Operations Associate II, you will support manufacturing operations through project leadership, process improvements, and cross-functional collaboration. Working closely with Manufacturing, MSAT, Quality, Engineering, Validation, and Project Management teams, you will help drive operational readiness, solve technical challenges, and improve manufacturing processes. This role is ideal for someone who enjoys balancing technical problem-solving with project ownership while contributing to the production of life-changing therapies.
This role follows a Monday through Friday standard business hours schedule.
What you will get:
  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Compensation programs that recognize performance
  • Medical, dental, and vision insurance
  • Opportunities to grow and develop your career
  • A collaborative and team-focused environment
  • The opportunity to support the delivery of life-changing therapies

What you will do:
  • Lead and support projects focused on process improvements, operational readiness, and manufacturing efficiency
  • Manage project timelines, deliverables, KPIs, and change control activities
  • Analyze manufacturing processes and equipment to identify opportunities for improvement
  • Support investigations related to manufacturing events, quality issues, and operational challenges
  • Collaborate with Manufacturing, Quality, Engineering, Validation, and MSAT teams to achieve project goals
  • Support technical transfers and departmental readiness activities for new campaigns and processes
  • Participate in risk assessments and help drive CAPA actions to completion
  • Review and support manufacturing documentation, including SOPs, work instructions, batch records, and change requests
  • Support equipment implementation, commissioning activities, and small equipment procurement projects
  • Train and support manufacturing teams on new processes, procedures, and operational improvements

What we are looking for:
  • High school diploma • or equivalent required; Bachelor's degree in a scientific, engineering, manufacturing, or related field preferred
  • 3-5 years of experience in biotechnology, pharmaceutical manufacturing, quality, engineering, or a related industry
  • Experience working in a GMP-regulated manufacturing environment
  • Experience leading or supporting projects and continuous improvement initiatives
  • Knowledge of manufacturing processes, change controls, investigations, CAPAs, and quality systems
  • Strong technical writing, organizational, and problem-solving skills
  • Strong communication and stakeholder management abilities
  • Proficiency with Microsoft Word, Excel, and PowerPoint
  • Familiarity with SAP or similar business systems is preferred

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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