ZipRecruiter

Log In

1

Quality Control Manager Jobs in Wells, ME (NOW HIRING)

Naderi Engineering, Inc.

Be Seen First

GMP Documentation - QC

Portsmouth, NH · On-site

$48.25/hr

Manage updates to raw-material specifications initiated through compliance records, management requests, change requests, or other approved channels. * Create and revise QC chemical raw-material ...

Lonza

QC Technical Services Analyst II

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Technical Services Analyst II - Large Scale Allogeneic (LSA) Project Location: Portsmouth, NH ... Sample Lifecycle Management: Execute precise sample receipt, login, and temperature-controlled ...

Kellton Tech

QC Analyst III - Portsmouth, NH

Portsmouth, NH · On-site

$35 - $40/hr

Title: QC Analyst III Location: Portsmouth, NH Pay rate range: $35/hr - $40/hr Duration: 12 months ... Quality Systems & Documentation Write and manage Quality Records, including Deviations, CAPAs, and ...

Lonza

QC Senior Scientist- Raw Materials

Portsmouth, NH · On-site

$90 - $120/hr

Working within the Quality Control team, you will perform laboratory testing, support method ... Strong organizational and time management skills with the ability to manage multiple priorities

MMQCI

QC Technical Lead

Saco, ME · On-site

$65K - $124K/yr

MMQCI is seeking a Quality Control Technical Lead who enjoys overseeing and executing quality ... This role reports to the Manager of Manufacturing Operations and is expected to work independently ...

New

previous page

Showing results 41-60

All JobsQuality Control JobsQuality Control Manager JobsQuality Control Manager Jobs in Wells, ME

Quality Control Manager information

See Wells, ME salary details

$32.1K

$85.7K

$136.4K

How much do quality control manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for quality control manager in Wells, ME is $85,656.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,700.00 and $105,300.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

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

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.

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

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

Is a Quality Control Manager a high paying job?

A Quality Control Manager typically earns a salary above the national average for managerial roles, with pay varying based on industry, experience, and location. They often require skills in inspection, testing, and quality assurance, and may hold certifications such as Six Sigma or ISO auditor training. Overall, it is considered a well-compensated position within manufacturing, production, and related sectors.

What is the work of a quality control manager?

A quality control manager oversees the inspection and testing of products or services to ensure they meet quality standards and specifications. They develop quality control procedures, analyze data, and coordinate with production teams to address issues, often using tools like inspection equipment and quality management systems. The role requires attention to detail, problem-solving skills, and knowledge of industry regulations.
More about Quality Control Manager jobs

What cities near Wells, ME are hiring for Quality Control Manager jobs?

Cities near Wells, ME with the most Quality Control Manager job openings:

Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Wells, ME as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 6% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $85,656 per year, or $41.2 per hour.

GMP Documentation - QC

Naderi Engineering, Inc.

Portsmouth, NH • On-site

$48.25/hr

Contractor

Medical, Dental, Vision

Posted 8 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.

Job description

QC Specialist III – Documentation

Location: Portsmouth, New Hampshire

Position Summary

We are seeking a detail-oriented QC Specialist III – Documentation to support Quality Control documentation and chemical raw-material specifications within a regulated pharmaceutical or biotechnology manufacturing environment.

This position is responsible for creating, maintaining, and updating raw-material specifications using a Document Management System (DMS) and Management System Laboratory Information Management System (LIMS). The successful candidate will work closely with QC Raw Material Scientists, Coordinators, Quality Assurance, and other cross-functional stakeholders to ensure specifications are accurate, functional, compliant, and suitable for supporting site manufacturing operations.

Key Responsibilities

  • Manage updates to raw-material specifications initiated through compliance records, management requests, change requests, or other approved channels.
  • Create and revise QC chemical raw-material specifications.
  • Create and update LIMS templates for new and existing raw materials.
  • Collaborate with Raw Material Scientists and Coordinators to develop clear and effective testing specifications.
  • Communicate specification changes and compliance-record requirements to cross-functional stakeholders.
  • Ensure approved changes are accurately and effectively implemented.
  • Own or maintain specification documents, SOPs, work instructions, and other controlled documents.
  • Review and edit technical documents for accuracy, consistency, clarity, and compliance.
  • Apply data-integrity principles in accordance with applicable policies, procedures, and regulatory expectations.
  • Support document change-control and document-management activities.
  • Track assigned projects and documentation updates to ensure deadlines are met.
  • Identify opportunities to improve and streamline documentation processes.
  • Follow applicable cGMP, quality, environmental, health, and safety requirements.
  • Promptly escalate significant GMP deficiencies, process deviations, product-quality concerns, and documentation issues.
  • Perform other duties as assigned.

Required Qualifications

  • Associate degree in science or a related field.
  • A combination of relevant education and professional experience may be considered.
  • Minimum of two years of document editing, document control, or regulated-industry experience.
  • Experience working in a pharmaceutical, biotechnology, medical-device, or other regulated environment.
  • Knowledge of current Good Manufacturing Practices (cGMP).
  • Experience using document management systems and following document-control practices.
  • Experience with document change management.
  • Strong technical writing experience involving specifications, methods, protocols, or reports.
  • Advanced proficiency with Microsoft Office, particularly Word and Excel.
  • Excellent proofreading, editing, and attention-to-detail skills.
  • Ability to accurately interpret written and verbal instructions.
  • Business-fluent English communication skills.

Preferred Qualifications

  • Experience working with LIMS and creating or maintaining LIMS templates.
  • Knowledge of compendial requirements, including USP and EP.
  • Experience supporting QC raw-material testing or specification management.
  • Familiarity with data-integrity requirements in a cGMP laboratory or manufacturing environment.
  • Experience collaborating with Quality Control, Quality Assurance, Technical Transfer, and cross-functional teams.

Key Competencies

  • Strong organization and document-management skills.
  • Ability to manage competing priorities and meet tight deadlines.
  • Clear written and verbal communication.
  • Ability to adapt to changing priorities and customer requirements.
  • Strong collaboration and internal customer-service skills.
  • Commitment to accuracy, quality, and regulatory compliance.
  • Ability to independently drive assignments through completion.

Physical and Work Requirements

  • Ability to work in a busy environment with tight deadlines and fluctuating workloads.
  • Regular sitting and occasional standing, walking, reaching, bending, kneeling, squatting, stair climbing, ladder climbing, driving, and gowning.
  • Ability to occasionally lift up to 50 pounds.
  • Must complete required health and safety training and comply with all site safety procedures.