Quality Assurance Specialist Jobs in New Hampshire
Quality Assurance Specialist jobs in New Hampshire concentrate heavily in advanced manufacturing, medical devices, defense electronics, and life sciences, with the strongest demand running from entry-level QA technicians through senior quality engineers. Manchester, Nashua, and the southern tier corridor anchor most hiring activity, where established employers like BAE Systems, Benchmark Electronics, and Dartmouth Health maintain large operations that depend on consistent quality oversight. Software-driven quality assurance, ISO 13485 compliance, and process validation are the specialties drawing the most consistent attention from New Hampshire hiring managers right now. Find a role that fits below and apply directly.
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Showing 5 of 12+ Quality Assurance Specialist 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 12 Quality Assurance Specialist Jobs in New Hampshire
Find roles in New Hampshire that match your experience and apply in just a few clicks.
Find JobsQuality Assurance Specialist Jobs by City in New Hampshire
Where New Hampshire roles are concentrated, by current openings.
Quality Assurance Specialist Job Market in New Hampshire
A snapshot from current New Hampshire openings, updated as new roles post.
Who's Hiring
- PCI Pharma Services5
- Lonza2
- CANAM1
- Cimetrics1
- BAE Systems USA1
Top Industries Hiring
- Manufacturing2
- Biotechnology & Pharmaceuticals2
- Energy1
What New Hampshire Employers Look For
The qualifications that appear most often in quality assurance specialist jobs across New Hampshire.
- Bachelor's degree in engineering, life sciences, or a related technical field required
- Hands-on experience with ISO 9001 or AS9100 quality management systems preferred
- Proficiency with inspection tools, CMMs, or statistical process control software expected
- Familiarity with FDA 21 CFR Part 820 or ISO 13485 for medical device roles
- Strong documentation skills including writing NCRs, CAPAs, and audit reports
- ASQ Certified Quality Auditor or Certified Quality Engineer credential viewed favorably
Quality Assurance Specialist Jobs in New Hampshire: Frequently Asked Questions
How do you become a quality assurance specialist in New Hampshire?
Most quality assurance specialist roles in New Hampshire require a bachelor's degree in engineering, manufacturing technology, or a related field, though associate degrees paired with strong technical experience are accepted by many manufacturers. New Hampshire does not issue a state license specifically for quality assurance specialists, so employers focus on certifications from the American Society for Quality, such as the CQE or CQA, which are widely recognized across the state's defense, medical device, and advanced manufacturing sectors.
Which companies hire quality assurance specialists in New Hampshire?
New Hampshire quality assurance specialist roles are posted by PCI Pharma Services, Lonza, and CANAM and others right now, based on current listings on Migrate Mate as of July 2026. New Hampshire's concentration of defense contractors, medical device firms, and precision manufacturers in the Nashua and Manchester area means that quality assurance hiring here tends to be steady and technically demanding year-round.
Which New Hampshire cities have the most quality assurance specialist jobs?
Bedford, Portsmouth, and Hudson account for the largest share of quality assurance specialist openings in New Hampshire. Manchester and Nashua drive the bulk of demand because southern New Hampshire hosts the state's densest cluster of defense electronics, medical device, and precision manufacturing employers, while smaller cities like Concord and Portsmouth add openings through healthcare systems, state government contractors, and aerospace suppliers operating in those areas.
Are there remote quality assurance specialist jobs in New Hampshire?
Yes, but they're limited. Quality assurance specialist work often involves hands-on inspection, supplier audits, and production floor oversight that requires physical presence. About 0% of quality assurance specialist openings tied to New Hampshire are remote or hybrid as of July 2026, and those positions tend to cover document control, supplier quality management, or quality systems roles where the core work is review and analysis rather than direct product inspection.
How can I get hired as a quality assurance specialist in New Hampshire with little or no experience?
The most realistic entry point is a QA technician or quality inspector role at one of New Hampshire's advanced manufacturers, where employers like BAE Systems and medical device firms in the Nashua corridor regularly hire candidates with a technical associate degree or a completed engineering technology program from a school like NHTI or Manchester Community College. Gaining an ASQ entry-level credential or completing a co-op through the University of New Hampshire's engineering program gives candidates a meaningful edge, and lateral moves from production technician or lab assistant roles are a common path in.
Where can I find and apply to quality assurance specialist jobs in New Hampshire?
You can find and apply to quality assurance specialist jobs in New Hampshire on Migrate Mate, which lists current openings across the state. Search the listings, find roles that match your background and location, and apply directly to the ones that fit.
See All 12 Quality Assurance Specialist Jobs in New Hampshire
Find roles in New Hampshire that match your experience and apply in just a few clicks.
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