1

Final Quality Control Inspector Jobs in Fall River, MA

Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Inspection Readiness * Support internal and external audits by clearly communicating investigation ...

Specialist QC

West Greenwich, RI · On-site

$95 - $125/hr

Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Inspection Readiness * Support internal and external audits by clearly communicating investigation ...

Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Inspection Readiness * Support internal and external audits by clearly communicating investigation ...

Coordinate and perform analysis on incoming, in-process, and final product samples. Testing is conducted in designated Quality Control (QC) laboratories and serves as critical quality checkpoints ...

Identify areas for quality control improvement and implement new methods * Perform special ... final production, assembly, and ongoing strategic demand planning. Compensation Employee Type:

Be Seen First

Quality Control & Standards: * * Perform pre-paint and final Quality Control (QC) inspections to ensure all repairs comply with OEM repair procedures and safety guidelines. * Enforce shop safety ...

Be Seen First

Looking for experienced Quality Control Assistant. Must be trained in Geometrical Dimensioning and ... Ideal candidate will have training and experience with inspection of products produced by machine ...

... Process, and Final Inspections on Machines Parts - Ability to interpret blueprints, work ... of daily Quality Control functions to include: - Discusses inspection results with those ...

... Process, and Final Inspections on Machines Parts - Ability to interpret blueprints, work ... of daily Quality Control functions to include: - Discusses inspection results with those ...

... Process, and Final Inspections on Machines Parts - Ability to interpret blueprints, work ... of daily Quality Control functions to include: - Discusses inspection results with those ...

Showing results 41-60

Final Quality Control Inspector information

See Fall River, MA salary details

$11

$21

$33

How much do final quality control inspector jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for final quality control inspector in Fall River, MA is $21.56, according to ZipRecruiter salary data. Most workers in this role earn between $17.36 and $24.13 per hour, depending on experience, location, and employer.

What does a final quality control inspector do?

A Final Quality Control Inspector is responsible for examining finished products to ensure they meet specified quality standards before they are shipped to customers. They inspect items for defects, verify compliance with safety and quality guidelines, and document any issues found during the inspection process. Their work helps ensure that only products meeting the company’s quality requirements reach the market, reducing returns and enhancing customer satisfaction. Final Quality Control Inspectors may also recommend improvements to production processes to prevent future defects.

What skills and qualifications are needed to be a final quality control inspector?

To thrive as a Final Quality Control Inspector, you need a keen eye for detail, strong understanding of quality assurance standards, and typically a high school diploma or technical certification. Familiarity with inspection tools (like calipers, micrometers), quality management systems (such as ISO 9001), and reporting software is commonly required. Excellent communication, critical thinking, and problem-solving skills help inspectors document findings and collaborate effectively with production teams. These skills are crucial to ensure products meet required specifications and maintain customer satisfaction and regulatory compliance.

What are common challenges faced by final quality control inspectors and how are they addressed?

Final Quality Control Inspectors often face challenges such as identifying subtle defects in products under tight deadlines and maintaining consistency across large production batches. To address these, inspectors use standardized checklists, precision measuring tools, and collaborate closely with production teams to ensure clear communication about quality standards. Continuous training and adherence to quality protocols also help inspectors stay updated on best practices and improve their accuracy, making it easier to uphold rigorous quality requirements.

What is the difference between Final Quality Control Inspector vs Quality Assurance Inspector?

AspectFinal Quality Control InspectorQuality Assurance Inspector
CertificationsOften requires quality control certifications (e.g., CQI, ASQ)May also hold similar certifications, with additional focus on QA processes
Work EnvironmentWorks at the end of production lines, inspecting finished productsInvolved throughout the production process, ensuring quality standards are met
Industry UsageCommon in manufacturing, aerospace, automotive sectorsUsed across manufacturing, pharmaceuticals, and food industries
Primary FocusDetects defects in finished products before shipmentDevelops and implements quality systems to prevent defects

While both roles focus on quality, the Final Quality Control Inspector primarily inspects finished products for defects, whereas the Quality Assurance Inspector works proactively to develop processes that prevent defects throughout production.

Is final quality control inspection a good career?

Final quality control inspection is a stable career that involves reviewing products for defects and ensuring standards are met, often requiring attention to detail and familiarity with inspection tools. It can offer steady employment with opportunities for advancement and certification, such as Six Sigma or ISO standards, depending on the industry. The role typically involves working in manufacturing or production environments and may require shift work or physical stamina.

What cities near Fall River, MA are hiring for Final Quality Control Inspector jobs?

Cities near Fall River, MA with the most Final Quality Control Inspector job openings:

Specialist QC

Amgen, Inc.

West Greenwich, RI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 11 days ago


Job description

Career Category
Operations
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Specialist QC
What you will do
Let's do this. Let's change the world. In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen.
Responsibilities:
Analytical Investigation Ownership
  • Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results.
  • Perform scientifically sound root cause analysis and develop effective corrective and preventive actions (CAPAs).
  • Ensure investigations are completed accurately, on time, and in compliance with GMP requirements and internal quality standards.

Quality Systems & Risk Assessment
  • Own and support deviations, CAPAs, and effectiveness verifications as assigned.
  • Review and approve equipment-related change controls, as applicable.
  • Partner with Quality Assurance to ensure investigation outcomes are risk-based and inspection-ready.
  • May support additional project-based assignments as required.

Cross-Functional Collaboration
  • Collaborate with Quality Control laboratories, Manufacturing, Process Development, Quality Assurance, Supply Chain, and other functional groups to resolve complex quality events.
  • Facilitate effective communication among stakeholders to ensure timely investigation progression and issue resolution.
  • Engage subject matter experts as needed to support technically complex investigations.

Inspection Readiness
  • Support internal and external audits by clearly communicating investigation findings, root cause, and CAPA effectiveness.
  • Maintain complete, accurate, and inspection-ready documentation.

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a collaborative teammate with these qualifications.
Basic Qualifications
  • High school diploma/GED and 10 years of directly related experience OR
  • Associate's degree and 8 years of directly related experience OR
  • Bachelor's degree and 4 years of directly related experience OR
  • Master's degree and 2 years of directly related experience OR
  • Doctorate degree

Preferred Qualifications
  • Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or another Life Science discipline.
  • 5-8+ years of Quality Control or Quality Assurance experience within the biotechnology or pharmaceutical industry.
  • Demonstrated experience leading complex laboratory investigations, including OOS, OOT, atypical results, and laboratory deviations.
  • Strong knowledge of GMP regulations, laboratory quality systems, and deviation management processes.
  • Experience performing root cause analysis using structured problem-solving methodologies.
  • Strong understanding of analytical laboratory techniques, instrumentation, and data integrity principles.
  • Experience authoring and managing deviations, CAPAs, change controls, and effectiveness verifications.
  • Ability to evaluate technical data, assess risk, and make sound, science-based decisions.
  • Strong written and verbal communication skills with the ability to influence cross-functional teams.
  • Experience supporting regulatory inspections and responding to auditor inquiries.
  • Experience utilizing digital tools, data analytics, or AI-enabled technologies to improve laboratory processes is preferred.

What you can expect from us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Salary Range
100,450.45USD -135,903.55 USD