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Quality Assurance Program Manager Jobs in Wells, ME

High Liner Foods

QA Technician

Portsmouth, NH · On-site

Perform assigned quality, food safety, GMP, prerequisite program, and HACCP verification activities ... Manager. * Participate in Tier meetings or shift handoffs as needed to communicate quality ...

High Liner Foods

QA Technician

Portsmouth, NH

Perform assigned quality, food safety, GMP, prerequisite program, and HACCP verification activities ... Manager. * Participate in Tier meetings or shift handoffs as needed to communicate quality ...

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All JobsQuality Assurance Program JobsQuality Assurance Program Manager JobsQuality Assurance Program Manager Jobs in Wells, ME

Quality Assurance Program Manager information

See Wells, ME salary details

$40K

$124.4K

$188.5K

How much do quality assurance program manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for quality assurance program manager in Wells, ME is $124,364.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,400.00 and $152,200.00 per year, depending on experience, location, and employer.

What does a quality assurance program manager do?

A Quality Assurance Program Manager oversees the development and implementation of quality assurance processes within an organization. They ensure that products or services meet established standards of quality, reliability, and performance. This role involves coordinating QA teams, developing testing strategies, analyzing data, and working closely with other departments to resolve quality issues. They also play a key role in continuous improvement by identifying trends and recommending process enhancements. Ultimately, they help ensure customer satisfaction and regulatory compliance.

What are the key skills and qualifications needed to thrive as a quality assurance program manager?

To thrive as a Quality Assurance Program Manager, you need expertise in quality management systems, process improvement, and a relevant bachelor's degree, often in engineering or a related field. Familiarity with tools like ISO 9001 standards, Six Sigma methodologies, and QA software platforms such as Jira or Quality Center is typically required, along with certifications like ASQ or Six Sigma Black Belt. Strong leadership, analytical thinking, and effective communication skills help you manage teams and collaborate across departments. These skills ensure that quality standards are met, risks are mitigated, and products or services consistently meet customer and regulatory requirements.

How does a quality assurance program manager typically collaborate with cross-functional teams to ensure product quality?

A Quality Assurance Program Manager frequently partners with departments such as product development, engineering, and operations to embed quality standards throughout the product lifecycle. They facilitate regular meetings, coordinate testing schedules, and align on quality metrics to ensure everyone is working toward the same goals. This collaborative approach helps quickly identify and address potential issues, streamlining the path to consistent, high-quality outcomes. Effective communication and relationship-building are essential skills for managing these cross-functional efforts.

What is the difference between Quality Assurance Program Manager vs Quality Control Supervisor?

AspectQuality Assurance Program ManagerQuality Control Supervisor
CertificationsASQ CQE, Six Sigma, PMPISO 9001, Six Sigma, CQE (optional)
Work EnvironmentOversees quality systems across departments, strategic planningSupervises daily inspection and testing activities
Employer & Industry UsageManufacturing, aerospace, healthcare, softwareManufacturing, production, industrial settings

The Quality Assurance Program Manager focuses on developing and maintaining quality systems and processes, ensuring compliance and continuous improvement. In contrast, the Quality Control Supervisor manages daily inspection and testing to ensure products meet quality standards. Both roles are essential in quality management but differ in scope and responsibilities.

Is a quality assurance program manager a stressful job?

A quality assurance program manager role can be stressful due to the responsibility of ensuring product quality, meeting deadlines, and managing cross-functional teams. The job often requires attention to detail, problem-solving skills, and the ability to handle pressure during audits or product launches.

What job categories do people searching Quality Assurance Program Manager jobs in Wells, ME look for?

The top searched job categories for Quality Assurance Program Manager jobs in Wells, ME are:

Quality Assurance Program Manager jobs near you
Infographic showing various Quality Assurance Program Manager job openings in Wells, ME as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $124,364 per year, or $59.8 per hour.

Quality Assurance (QA) Roles (Entry to Mid-Level) (Night-Shift)

Lonza

Portsmouth, NH • On-site

Full-time

Posted 13 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

We're Hiring: Quality Assurance (QA) Professionals - Multiple Levels & Areas
Join our team and grow your career in Quality! We have exciting QA opportunities across multiple functions and levels, supporting both Cell Therapy and Biologics operations.
Job Summary - Quality Assurance (QA) Roles (Entry to Mid-Level)
The Quality Assurance (QA) function is responsible for ensuring that all products, processes, and systems comply with internal standards, regulatory requirements, and industry best practices. QA professionals support quality and compliance activities across manufacturing, laboratory, and operational environments, with responsibilities that may include compliance oversight, deviation management, investigations, batch record review, on-the-floor quality support, and project or program management.
At the entry level, QA professionals focus on executing routine quality tasks such as reviewing documentation, supporting Good Manufacturing Practice (GMP) compliance, assisting with investigations, and ensuring adherence to Standard Operating Procedures (SOPs). As experience grows, individuals take on increased ownership in deviation investigations, CAPA management, audit readiness, and cross-functional collaboration.
Mid-level QA professionals are expected to lead complex investigations, manage quality systems, support regulatory inspections, and drive continuous improvement initiatives. They may also oversee quality-related projects or programs, partner with manufacturing and technical teams, and provide guidance to junior staff. Roles such as QA Project Manager and QA Program Manager involve coordinating cross-functional efforts, managing timelines, mitigating risks, and ensuring successful delivery of quality and compliance objectives.
Across all levels, QA team members play a critical role in maintaining product quality, ensuring patient safety, and supporting regulatory compliance in a fast-paced, highly regulated environment.
Key Responsibilities (may vary by role and level):
  • Ensure compliance with GMP, regulatory requirements, and internal quality standards
  • Review and approve batch records, protocols, reports, and quality documentation
  • Support and/or lead deviation investigations, root cause analysis, and CAPA implementation
  • Provide on-the-floor QA support to manufacturing and operations teams
  • Participate in audits and inspections (internal, client, and regulatory)
  • Monitor quality metrics and identify opportunities for continuous improvement
  • Support change controls, risk assessments, and validation activities
  • Collaborate cross-functionally with Manufacturing, QC, Regulatory, and Engineering teams
  • Lead or support quality-related projects and programs, including timeline and risk management

Basic Qualifications (Entry-Level):
  • Bachelor's degree in Life Sciences, Engineering, or related field (or equivalent experience)- A combination of education and years of experience will be considered.
  • Strong attention to detail and organizational skills
  • Basic understanding of GMP or regulated environments preferred
  • Ability to follow SOPs and accurately document work
  • Strong communication and willingness to learn

Preferred Qualifications (Mid-Level):
  • 3-7+ years of experience in QA within a GMP-regulated industry
  • Hands-on experience with deviations, investigations, CAPAs, and change controls
  • Experience with batch record review and quality systems
  • Familiarity with audits and regulatory inspections
  • Experience with systems such as TrackWise, Veeva, LIMS, or similar

Key Skills and Competencies:
  • Strong knowledge of GMP and quality systems
  • Critical thinking and problem-solving skills
  • Attention to detail and data integrity mindset
  • Effective communication and cross-functional collaboration
  • Ability to manage multiple priorities and meet deadlines
  • Decision-making and risk assessment capabilities
  • Project management skills (for mid-level and above roles)
  • Continuous improvement mindset

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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