Quality Assurance Auditor Jobs in New Hampshire
Quality Assurance Auditor jobs in New Hampshire are concentrated in Manchester, Nashua, and Concord, where manufacturing, healthcare, and financial services firms maintain active compliance and audit functions. Major employers with a lasting New Hampshire presence include BAE Systems, Fidelity Investments, and Dartmouth Health, all of which hire quality assurance auditors across product quality, regulatory compliance, and process audit specialties. Openings range from entry-level audit associates to senior compliance auditors. Scan the live roles below and apply to whichever ones fit.
Find JobsOverview
Showing 5 of 18+ Quality Assurance Auditor jobs
Quality Assurance Manager, 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 you will do:
We are seeking an experienced Quality Assurance Manager, Operations to lead a team supporting GMP compliance and quality oversight across site operations. This role is responsible for ensuring quality objectives are achieved, supporting cross-functional teams, and promoting a strong culture of quality and continuous improvement. The ideal candidate will bring leadership experience within a regulated manufacturing environment and the ability to effectively manage priorities, people, and processes.
Lead and manage a team of QA Compliance Specialists and QA Project Managers, ensuring timely and effective delivery of quality objectives
Provide guidance and act as a point of escalation for quality-related issues impacting internal and external stakeholders
Ensure alignment with regulatory requirements, customer Quality Agreements, and internal SOPs across all QA activities
Partner cross-functionally with Manufacturing, MSAT, Engineering, QC, Validation, and Supply Chain to resolve complex quality issues
Support and participate in key quality forums, including Change Control, Deviations Review Board, CAPA Board, and Site Quality Council
Oversee and track quality metrics, including deviation trending and performance indicators, to support continuous improvement
Perform and support lot release and disposition activities in accordance with GMP standards
Drive continuous improvement initiatives to enhance quality systems, processes, and overall site compliance
What we are looking for:
5–10 years of experience in quality assurance within a biotechnology, pharmaceutical, or regulated manufacturing environment
Proven experience managing and developing teams, including coaching, performance management, and talent development
Strong knowledge of GMP regulations, quality systems, and compliance requirements
Experience supporting or leading investigations, deviations, CAPA, and change control processes
Ability to effectively collaborate with cross-functional teams and influence decision-making in a matrixed environment
Strong organizational and analytical skills, with the ability to manage multiple priorities and meet deadlines
Excellent communication skills, with the ability to engage effectively across all levels of the organization
Experience with systems such as TrackWise, SAP, Syncade, and Microsoft Office tools 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.
Quality Assurance Manager, 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 you will do:
We are seeking an experienced Quality Assurance Manager, Operations to lead a team supporting GMP compliance and quality oversight across site operations. This role is responsible for ensuring quality objectives are achieved, supporting cross-functional teams, and promoting a strong culture of quality and continuous improvement. The ideal candidate will bring leadership experience within a regulated manufacturing environment and the ability to effectively manage priorities, people, and processes.
Lead and manage a team of QA Compliance Specialists and QA Project Managers, ensuring timely and effective delivery of quality objectives
Provide guidance and act as a point of escalation for quality-related issues impacting internal and external stakeholders
Ensure alignment with regulatory requirements, customer Quality Agreements, and internal SOPs across all QA activities
Partner cross-functionally with Manufacturing, MSAT, Engineering, QC, Validation, and Supply Chain to resolve complex quality issues
Support and participate in key quality forums, including Change Control, Deviations Review Board, CAPA Board, and Site Quality Council
Oversee and track quality metrics, including deviation trending and performance indicators, to support continuous improvement
Perform and support lot release and disposition activities in accordance with GMP standards
Drive continuous improvement initiatives to enhance quality systems, processes, and overall site compliance
What we are looking for:
5–10 years of experience in quality assurance within a biotechnology, pharmaceutical, or regulated manufacturing environment
Proven experience managing and developing teams, including coaching, performance management, and talent development
Strong knowledge of GMP regulations, quality systems, and compliance requirements
Experience supporting or leading investigations, deviations, CAPA, and change control processes
Ability to effectively collaborate with cross-functional teams and influence decision-making in a matrixed environment
Strong organizational and analytical skills, with the ability to manage multiple priorities and meet deadlines
Excellent communication skills, with the ability to engage effectively across all levels of the organization
Experience with systems such as TrackWise, SAP, Syncade, and Microsoft Office tools 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.
See All 18 Quality Assurance Auditor Jobs in New Hampshire
Find roles in New Hampshire that match your experience and apply in just a few clicks.
Find JobsQuality Assurance Auditor Jobs by City in New Hampshire
Where New Hampshire roles are concentrated, by current openings.
Quality Assurance Auditor Job Market in New Hampshire
A snapshot from current New Hampshire openings, updated as new roles post.
Who's Hiring
- PCI Pharma Services5
- Lonza2
- Extreme Networks2
- CANAM1
- Getinge1
Top Industries Hiring
- Manufacturing2
- Electronics & Hardware2
- Biotechnology & Pharmaceuticals2
- Energy1
- Education1
What New Hampshire Employers Look For
The qualifications that appear most often in quality assurance auditor jobs across New Hampshire.
- Bachelor's degree in quality management, engineering, business, or a related field required
- Certified Quality Auditor credential from ASQ preferred or required by most employers
- Demonstrated experience conducting internal audits against ISO 9001 or similar frameworks
- Proficiency with quality management systems software such as ETQ or MasterControl
- Strong written communication skills for producing clear audit findings and corrective action reports
- Familiarity with FDA 21 CFR Part 820 or GMP requirements for medical device or pharma roles
Quality Assurance Auditor Jobs in New Hampshire: Frequently Asked Questions
How do you become a quality assurance auditor in New Hampshire?
Most quality assurance auditor positions in New Hampshire require a bachelor's degree in a technical or business discipline, followed by experience in a quality or compliance role. New Hampshire does not issue a state license specific to quality auditors, but the Certified Quality Auditor credential from the American Society for Quality is the industry standard that New Hampshire employers consistently expect. Candidates from manufacturing, healthcare, or financial services backgrounds transition most readily into these roles.
How much do quality assurance auditors make in New Hampshire?
Quality assurance auditors in New Hampshire earn a median of about $82,800 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $54,980 for the lowest 10% to over $123,020 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire quality assurance auditors in New Hampshire?
Companies currently hiring quality assurance auditors in New Hampshire include PCI Pharma Services, Lonza, and Extreme Networks, per current listings on Migrate Mate as of July 2026. New Hampshire's manufacturing corridor along the Merrimack Valley and its growing healthcare network make it one of the more consistent states for audit and compliance hiring in New England.
Which New Hampshire cities have the most quality assurance auditor jobs?
Bedford, Salem, and Merrimack hold the most quality assurance auditor openings in New Hampshire. Manchester and Nashua dominate because they anchor the state's manufacturing and financial services sectors, while Concord draws audit roles tied to state government contractors and healthcare administration. Smaller southern New Hampshire communities often appear in listings because of their proximity to Boston-area employers with New Hampshire operations.
Are there remote quality assurance auditor jobs in New Hampshire?
Yes, though availability depends heavily on the industry, since roles tied to physical product inspection or on-site facility audits are rarely remote while compliance documentation and system audit work is more portable. About 8% of quality assurance auditor openings tied to New Hampshire are remote or hybrid as of July 2026, which reflects that split. Financial services and software quality roles account for most of the fully remote postings.
How can I get hired as a quality assurance auditor in New Hampshire with little or no experience?
The most realistic entry path is a quality technician or quality inspector role at one of New Hampshire's manufacturing firms, where you gain hands-on documentation and process review experience before moving into auditing. BAE Systems and smaller precision manufacturers along the Merrimack Valley regularly hire quality associates with no prior audit experience. Completing the ASQ Certified Quality Improvement Associate exam before applying signals commitment and gives you a concrete edge over other entry-level candidates.
Where can I find and apply to quality assurance auditor jobs in New Hampshire?
You can find and apply to quality assurance auditor jobs in New Hampshire on Migrate Mate, which lists current openings across the state. Search the listings, identify the roles that match your background and location, and apply directly to the ones that fit.
See All 18 Quality Assurance Auditor Jobs in New Hampshire
Find roles in New Hampshire that match your experience and apply in just a few clicks.
Find Jobs