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

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing United States, Portsmouth (New ... CAPA & Change Control Management Author, edit, and coordinate corrective and preventive actions ...

QC Analyst IV

Portsmouth, NH · On-site

$24.50 - $32.75/hr

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Job Title: QC Analyst IV Location: Portsmouth, NH 03801 Duration: 8 Months Job Type: Temporary ...

QC Analyst III, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA ... CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions ...

QC Analyst III, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA ... CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions ...

QC Analyst III, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA ... CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions ...

QC Analyst III, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA ... CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions ...

QC Analyst II, Analytical - LSA

Portsmouth, NH

$24.50 - $32.75/hr

QC Analyst II, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA ... CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions ...

QC Analyst II, Analytical - LSA

Portsmouth, NH · On-site

$24.50 - $32.75/hr

QC Analyst II, Analytical - Large Scale Allogenic Manufacturing Location: Portsmouth, NH, USA ... CAPA & Change Control Management: Author, edit, and coordinate corrective and preventive actions ...

QC Analyst III

Portsmouth, NH · On-site

$25 - $30/hr

TekWissen group is a workforce management provider throughout the USA and many other countries in ... Job Title: QC Analyst III Location: Portsmouth, NH 03801 Duration: 12 months Job Type: Temporary ...

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC ... Use laboratory systems and software to record and manage data * Identify deviations and support ...

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC ... Use laboratory systems and software to record and manage data * Identify deviations and support ...

QC Analyst I-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst I - Microbial Control Location: Portsmouth, NH, (On-site) As a QC Analyst I ... Use laboratory systems and basic software to enter and manage data * Assist in identifying ...

QC Analyst I-Microbial Control

Portsmouth, NH

$24.50 - $32.75/hr

Quality Control Analyst I - Microbial Control Location: Portsmouth, NH, (On-site) As a QC Analyst I ... Use laboratory systems and basic software to enter and manage data * Assist in identifying ...

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC ... Use laboratory systems and software to record and manage data * Identify deviations and support ...

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Quality Control Analyst II - Microbial Control (Night) Location: Portsmouth, NH, (On-site) As a QC ... Use laboratory systems and software to record and manage data * Identify deviations and support ...

Showing results 21-40

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.

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

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

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.

QC Analyst III, Analytical - LSA

Lonza

Portsmouth, NH • On-site

$70 - $90/hr

Other

Medical, Dental, Vision, PTO

Re-posted 28 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

QC Analyst III, Analytical - Large Scale Allogenic Manufacturing

United States, Portsmouth (New Hampshire)

Location: Portsmouth, NH, USA.

Schedule: Monday - Friday, 0800-1700

We are seeking an advanced laboratory professional to join our Quality organization in Portsmouth, NH, as an Analyst III, QC Analytical. Operating under general supervision, this senior bench-based role executes critical cGMP release testing, handles method validation protocols, and drives complex laboratory investigations.

Advanced cGMP Release Testing

Execute complex biological, immunological, and cell-based testing—specifically utilizing flow cytometry, ELISA, PCR assays, cell culture, and cell counting—ensuring total compliance with internal SOPs, USP, and EP guidelines to support on-time in-process control and final product release.

Assay Transfer & Method Validation

Actively spearhead analytical method transfers, qualifications, and validation protocols, including onboarding new methodologies and configuring advanced laboratory instrumentation.

Data Review & Verification

Review raw laboratory records, data calculations, and execution logs for absolute accuracy, protocol compliance, and strict adherence to Good Documentation Practices (GDP).

Investigation & OOS Ownership

Lead comprehensive Out-of-Specification (OOS) and laboratory deviation investigations, leveraging root-cause analysis tools to address complex non-conformances with minimal support.

CAPA & Change Control Management

Author, edit, and coordinate corrective and preventive actions (CAPAs) and detail structured Change Controls to promote compliance and continuous laboratory improvement with minimal support.

Document Architecture

Develop, modify, and sustain standard operating procedures (SOPs), master forms, and test records to match evolving industry expectations and site improvements.

Peer Training & Floor Leadership

Deliver hands-on, on-the-job training for junior QC personnel, reviewing data packets, modeling strong work ethics, and escalating critical laboratory anomalies to management as needed.

What will you get?

An agile career and dynamic working culture

An inclusive and ethical workplace

Compensation programs that recognize high performance

Medical, dental and vision insurance, as well as PTO and more

What we’re looking for Experience

3-4+ years of direct Quality Control laboratory experience within a cGMP biomanufacturing or regulated clinical testing setting is required.

Technical Mastery

Proven, hands-on experience performing cell culture maintenance, immunophenotyping panels via flow cytometry, PCR amplification, and standard immunological assay techniques.

Systems & Digital Compliance

Familiarity with Laboratory Information Management Systems (LIMS), enterprise data management applications, and quality systems software (such as TrackWise) is highly preferred.

Investigation Savvy

Demonstrated ability to independently lead laboratory event investigations, formulate root-cause theories, and write clear, logical technical summaries.

Education

Bachelor’s Degree in Biochemistry, Biology, or a closely related technical science discipline is required. A Master’s Degree in a scientific discipline is preferred.

Soft Skills

Superior written and oral communication skills, a solutions-focused team attitude, and the personal initiative required to navigate multiple testing demands and overcome performance roadblocks without routine reminders.

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.

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