1

Process Quality Manager Jobs in Rochester, NH (NOW HIRING)

Process Engineer

Sanford, ME ยท On-site

$70K - $80K/yr

... quality, safety, and cost performance. Join a company committed to protecting scientists and ... SUMMARY The Process Engineer reports to the Manufacturing Operations Manager. The Process Engineer ...

Quality Assurance Engineer III

Concord, NH ยท On-site

$121K - $148K/yr

... processes. Support activities related to: Design and Development, Risk Management, Quality Engineering, Supplier Quality Agreements, Quality Inspection Planning, Quality Auditing, Supplier Management ...

You will perform first-article, in-process, and final inspections while working closely with ... quality management system.โ— Strong attention to detail and the ability to accurately document ...

You will perform first-article, in-process, and final inspections while working closely with ... quality management system. โ€ข Strong attention to detail and the ability to accurately document ...

You will perform first-article, in-process, and final inspections while working closely with ... quality management system. โ€ข Strong attention to detail and the ability to accurately document ...

You will perform first-article, in-process, and final inspections while working closely with ... quality management system.โ— Strong attention to detail and the ability to accurately document ...

Further strong project management skills with ability to manage tasks effectively * Familiarity ... We live our mission of making our world more productive every day by providing high-quality ...

Showing results 41-60

Process Quality Manager information

See Rochester, NH salary details

$33.3K

$99.6K

$163K

How much do process quality manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for process quality manager in Rochester, NH is $99,567.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,000.00 and $126,700.00 per year, depending on experience, location, and employer.

What is a process quality manager?

Process Quality Managers are professionals responsible for ensuring that an organization's processes and products meet established quality standards. They design and implement quality control procedures, monitor production processes, and work to identify areas for improvement. These managers also lead audits, analyze data to prevent defects, and collaborate with various departments to uphold compliance with industry regulations. Their goal is to maintain high levels of customer satisfaction by ensuring consistent product or service quality.

What are some common challenges faced by process quality managers, and how can they be addressed?

Process Quality Managers often encounter challenges such as resistance to change from team members, balancing strict quality standards with production efficiency, and managing cross-functional communication. To address these issues, successful managers proactively engage stakeholders, provide clear training on quality processes, and foster a culture of continuous improvement. Collaboration and transparent communication with production, engineering, and leadership teams are key to overcoming obstacles and ensuring that quality initiatives are effectively implemented.

What are the key skills and qualifications needed to thrive as a process quality manager, and why are they important?

To thrive as a Process Quality Manager, you need a strong background in quality management, process improvement methodologies (such as Six Sigma or Lean), and a relevant degree in engineering, manufacturing, or a related field. Familiarity with quality management systems (QMS), statistical process control (SPC) tools, and certifications like Six Sigma Green/Black Belt or ISO 9001 Auditor are typically required. Outstanding analytical thinking, problem-solving abilities, leadership, and effective communication are vital soft skills for this position. These competencies ensure that quality standards are consistently met, processes are optimized, and teams are aligned to achieve organizational goals.

What is the difference between Process Quality Manager vs Quality Assurance Specialist?

AspectProcess Quality ManagerQuality Assurance Specialist
CertificationsSix Sigma, Lean, ISO certificationsISO, Six Sigma, or QA-specific certifications
Work EnvironmentManufacturing, production, or operational settingsProduct development, software, or service industries
ResponsibilitiesOversees process improvements, ensures process compliance, manages quality metricsTests products/services, identifies defects, implements QA procedures

The Process Quality Manager focuses on optimizing and maintaining manufacturing or operational processes, ensuring efficiency and compliance. In contrast, the Quality Assurance Specialist concentrates on testing and verifying products or services to meet quality standards. Both roles require similar certifications and often work within manufacturing or production environments, but their core responsibilities differ in scope and focus.

What cities near Rochester, NH are hiring for Process Quality Manager jobs?

Cities near Rochester, NH with the most Process Quality Manager job openings:

Infographic showing various Process Quality Manager 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 $99,567 per year, or $47.9 per hour.

QA Compliance Specialist 2 - Portsmouth, NH

Portsmouth, NH โ€ข On-site

Unicon Pharma Inc.
Recruiting and Staffing Servicesย โ€ขย 11 - 50 employees

Contractor

Re-posted 7 days ago


Job description

Title - QA Specialist – QA compliance

Job Description:

  • The QA Specialist – QA Compliance is responsible for supporting and maintaining the site's Quality Management System (QMS) by ensuring alignment between local quality procedures and Client Group Quality Standards.
  • The role leads structured gap assessments of local procedures against Group procedures, identifies compliance gaps, coordinates remediation activities, and ensures timely implementation of required changes.
  • The position collaborates with Global Quality, Manufacturing, Quality Operations, Engineering, Regulatory Affairs, and other stakeholders to maintain compliance with corporate standards and applicable GMP regulations while driving continuous improvement.

Key Accountabilities:

  • Lead gap assessments of local Quality Management System procedures against Group Quality Procedures and Corporate Standards.
  • Coordinate updates to local SOPs, work instructions, and controlled documents.
  • Track implementation and drive completion to defined timelines.
  • Partner with process owners and SMEs to establish and implement compliant solutions.
  • Support Change Control, CAPA, Deviations, and Quality Risk Management activities.
  • Support internal audits and regulatory inspections.
  • Monitor compliance metrics and prepare management reports through trending and visual KPI management.
  • Develop and Provide training and guidance on new or revised quality procedures.
  • Drive continuous improvement and harmonization of Quality System processes

Skills:

  • Bachelor’s Degree or equivalent experience. Preferred area of study:  Scientific related field
  • 3-5 or more years in GMP environment. Minimum 0-3 years in Quality Assurance or similar discipline. Biotechnology manufacturing background is preferred
  • Knowledge of cGMP and regulations
  • Project Management Experience: Presentation, Customer Liaison, Meeting facilitation
  • Demonstrates flexibility to adapt to changing business priorities.  .
  • Demonstrate ability for effective Planning, Organizing and Controlling competency.
  • Demonstrate sound decision making, considering broad scope of factors.
  • Able to manage multiple priorities and achieve results.
  • Good ability to complete assignments under tight timelines, and work under pressure.
  • Demonstrates knowledge on continuous improvement within the adherence to standardized procedures & cGMP compliance
  • Experience with Trackwise, SAP, Document management system preferred.
  • Detail-oriented
  • Self-motivated
  • Displays a clear willingness to listen to others.
  • Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer focused,Practices safety awareness at all times.