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Software Quality Operations Associate Jobs in Exeter, NH

Eastern Bank

Operations Associate

Newburyport, MA · On-site

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Eastern Bank

Operations Associate

Newburyport, MA

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Eastern Bank

Operations Associate

Manchester, NH · On-site

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Eastern Bank

Operations Associate

North Andover, MA

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Eastern Bank

Operations Associate

Manchester, NH

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Eastern Bank

Operations Associate

North Andover, MA · On-site

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Eastern Bank

Operations Associate I

Salem, NH · On-site

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Eastern Bank

Operations Associate I

Salem, NH

$24.50/hr

The Operations Associate maintains primary responsibility for all operational elements of a small ... quality control processes around new account opening, and other such branch activities. Fully ...

Lonza

Strategic Operations Associate I

Portsmouth, NH · On-site

Strategic Operations Associate I Location: Portsmouth, NH (On-site) As a Strategic Operations ... Working with teams across Manufacturing, Quality, Engineering, and MSAT, you will help solve ...

Lonza

Strategic Operations Associate I

Portsmouth, NH · On-site

Strategic Operations Associate I Location: Portsmouth, NH (On-site) As a Strategic Operations ... Working with teams across Manufacturing, Quality, Engineering, and MSAT, you will help solve ...

VAPOTHERM, INC.

Legal Operations Associate

Exeter, NH · On-site

Highly organized, detail-oriented, and tech-savvy Legal Operations Associate to support our dynamic ... Software Administration * Administers and optimizes legal technology tools, including contract ...

Crateandbarrel

Operations Associate, C&B

Kittery, ME · On-site

Drawn together by a shared passion for our customers and a spirit of fun, we deliver high-quality ... As a C&B Operations Associate, you will play a vital role in maintaining an efficient stockroom and ...

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Software Quality Operations Associate information

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$27

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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:

Software Quality Operations Associate jobs near you
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.

Quality Operations Specialist

Merrimack Manufacturing

Manchester, NH • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

COMPANY OVERVIEW:
Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life.Position Summary
The Quality Operations Specialist is responsible for supporting manufacturing quality operations through comprehensive review of Device History Records (DHRs), product release activities, and production quality documentation. This role ensures that Merrimack Manufacturing products meet established quality requirements, regulatory standards, and internal procedures prior to release for distribution.
The Quality Operations Specialist serves as a key quality representative within manufacturing operations and works closely with Production, Engineering, Supply Chain, and Quality teams to ensure timely review of production records, resolution of documentation issues, and compliant product disposition decisions. This position plays a critical role in maintaining compliance with ISO 13485, applicable regulatory requirements, and company quality standards.
Responsibilities
Device History Record (DHR) Review
  • Perform detailed reviews of Device History Records (DHRs) to ensure completeness, accuracy, and compliance with approved procedures and manufacturing requirements.
  • Verify that all manufacturing, inspection, testing, labeling, and packaging activities have been completed and documented appropriately.
  • Review production records for compliance with specifications, acceptance criteria, and quality requirements.
  • Identify documentation discrepancies, missing information, and record errors requiring correction prior to release.
  • Coordinate with Manufacturing, Engineering, and Quality personnel to resolve DHR review findings in a timely manner.
  • Maintain accurate review documentation and release records in accordance with established procedures.

Product Release Activities
  • Perform product disposition and release activities in accordance with established quality system procedures.
  • Verify that all required inspections, testing, and acceptance activities have been successfully completed prior to product release.
  • Ensure all non-conformances, deviations, and quality events impacting product release have been appropriately addressed and documented.
  • Review quality data and supporting documentation to support release decisions.
  • Support timely release of finished goods while maintaining compliance with regulatory and quality requirements.
  • Escalate quality concerns or release risks to Quality leadership when appropriate.

Manufacturing Quality Support
  • Partner with manufacturing teams to ensure production documentation meets quality requirements.
  • Support resolution of documentation and recordkeeping issues identified during production and review activities.
  • Assist with implementation of process improvements related to manufacturing documentation and product release workflows.
  • Participate in production meetings and provide quality input regarding documentation and release readiness.

Quality System Compliance
  • Ensure activities comply with ISO 13485, FDA Quality System Regulation, and applicable internal procedures.
  • Support investigations related to documentation errors, record discrepancies, and product release issues.
  • Participate in internal audits and inspection readiness activities related to manufacturing records and product release processes.
  • Support CAPA, nonconformance, and change control activities as assigned.

Metrics and Continuous Improvement
  • Track and report DHR review and product release metrics.
  • Identify recurring documentation issues and opportunities for process improvement.
  • Support continuous improvement initiatives to improve record accuracy, review efficiency, and overall quality system effectiveness.
  • Assist in development and implementation of best practices for manufacturing documentation and product release activities.

Qualifications & Skills
  • Associate degree in Quality, Engineering, Life Sciences, Manufacturing, or related field preferred. Equivalent combination of education and experience may be considered.
  • 2-5 years of experience in Quality Assurance, Manufacturing Quality, Production Quality, or Quality Systems within a regulated industry.
  • Experience reviewing manufacturing records, batch records, Device History Records (DHRs), or equivalent production documentation preferred.
  • Experience working within an ISO 13485 and/or FDA-regulated medical device environment preferred.
  • Familiarity with product release or product disposition processes preferred.
  • Strong attention to detail and documentation review skills.
  • Ability to identify discrepancies and assess compliance with established procedures.
  • Strong organizational and time management skills.
  • Effective written and verbal communication skills.
  • Proficiency with Microsoft Office applications and electronic quality management systems (eQMS) and ERP/MES systems.
  • Ability to work independently while managing multiple priorities in a fast-paced manufacturing environment.
Preferred Candidate Profile
  • Exceptional attention to detail and ability to identify discrepancies, omissions, and documentation errors.
  • Strong recordkeeping and documentation management skills with a demonstrated ability to maintain accurate, complete, and organized records.
  • Experience reviewing large volumes of documentation while maintaining a high degree of accuracy and consistency.
  • Ability to follow established procedures, work instructions, and quality requirements with minimal oversight.
  • Strong analytical and verification skills with a methodical and disciplined approach to work.
  • Experience in documentation review, document control, inventory control, production record review, bookkeeping, data entry, or other highly detail-oriented administrative functions is highly desirable.
  • Demonstrated ability to manage repetitive review activities while maintaining accuracy and compliance.
  • Strong organizational and time management skills with the ability to prioritize workload and meet release timelines.
  • Comfortable working with electronic quality systems, ERP systems, databases, and controlled documentation.

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