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Quality Control Investigator Jobs (NOW HIRING)

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Quality Control (QC) Chemist - Inhalation Products (MDI Focus) Location: Fall River, MA (On-site ... Investigate OOS, deviations, and atypical results , contributing to root cause analysis and ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

Quality Control (QC) Chemist - Inhalation Products (MDI Focus) Location: Fall River, MA (On-site ... Investigate OOS, deviations, and atypical results , contributing to root cause analysis and ...

Cipla

$65K - $105K/yr

Quality Control (QC) Chemist - Inhalation Products (MDI Focus) Location: Fall River, MA (On-site ... Investigate OOS, deviations, and atypical results, contributing to root cause analysis and ...

Techtrueup

Quality Control

Mebane, NC · On-site

$16.25 - $20.75/hr

Identify and document non-conforming materials and products. * Assist in root cause investigations ... Measurement Specialist (QC): Focuses on routine inspection activities, product verification ...

University of Colorado

Quality Control Supervisor

Aurora, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The QC supervisor ensures timely, compliant analytical support for a GMP-regulated clinical ... Quality Systems, Investigations, and Compliance Oversight (15%) * Draft, review, and manage ...

Techtrueup

Quality Control

Mebane, NC · On-site

$16.25 - $20.75/hr

Identify and document non-conforming materials and products. * Assist in root cause investigations ... Measurement Specialist (QC): Focuses on routine inspection activities, product verification ...

American Society for Quality

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead root cause investigations using structured problem-solving methodologies and statistical tools ... Experience linking QC trends, nonconformances, complaint investigations, and manufacturing ...

Techtrueup

Quality Control

Mebane, NC

$16.25 - $20.75/hr

Identify and document non-conforming materials and products. * Assist in root cause investigations ... Measurement Specialist (QC): Focuses on routine inspection activities, product verification ...

Enchanted Rock

Quality Control (QC) Supervisor

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The QC Supervisor will be a member of the Quality Team, reporting to the Quality Director. This ... Experience investigating quality issues and participating in root cause analysis and corrective ...

UFP Industries

Quality Control

Nappanee, IN · On-site

Job Summary The Quality Control Inspector is responsible for the measurement and visual inspection ... Assists in investigation of all quality issues and/or occurrences and ensures that corrective ...

Cashco

Quality Control (QC) Inspector

Ellsworth, KS

$19 - $27/hr

... investigate root causes of quality issues and recommend corrective actions. • Monitor rework or ... control professional. • Strong understanding of assembly processes, quality standards, and ...

Adecco

Quality Control

Londonderry, NH · On-site

$19 - $21/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Associate Shift: Monday - Friday | 4:00 PM - 12:30 AM Pay: $19-$21 Job Duties ... Investigate inventory variances and assist with corrective actions * Complete quality documentation ...

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Quality Control Investigator information

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How much do quality control investigator jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for quality control investigator in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality control investigator?

To thrive as a Quality Control Investigator, you need expertise in quality assurance processes, attention to detail, and a background in science or engineering, often supported by relevant certifications such as Six Sigma or ISO compliance. Familiarity with laboratory equipment, statistical analysis software, and quality management systems is typically required. Strong analytical thinking, problem-solving abilities, and effective communication are essential soft skills in this role. These competencies ensure that products and processes consistently meet regulatory standards and company expectations, minimizing errors and maintaining organizational integrity.

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

Quality Control Investigators often encounter challenges such as managing tight deadlines for investigating quality deviations, ensuring thorough documentation, and coordinating with multiple departments to collect necessary information. To address these, it's important to develop strong organizational skills, maintain clear communication channels, and stay current with regulatory requirements. Proactively collaborating with production, QA, and regulatory teams can help streamline investigations and lead to more effective root cause analysis and corrective actions.

What is the difference between Quality Control Investigator vs Quality Assurance Specialist?

AspectQuality Control InvestigatorQuality Assurance Specialist
CertificationsOften requires GMP, GLP, or ISO certificationsSimilar certifications, with additional focus on auditing
Work EnvironmentLaboratory, manufacturing, or production settingsOffice, laboratory, or production environments
Primary FocusInvestigating quality issues, deviations, and non-conformancesDeveloping and implementing quality systems and procedures
Employer & Industry UsagePharmaceutical, biotech, manufacturingPharmaceutical, biotech, manufacturing

Both roles are vital in quality management, but the Quality Control Investigator primarily focuses on identifying and resolving quality issues through investigations, while the Quality Assurance Specialist develops systems to prevent issues. They often work together to ensure product quality and compliance.

What is a quality control investigator?

Quality Control Investigators are professionals responsible for ensuring that products or services meet established quality standards and regulatory requirements. They inspect processes, materials, and finished goods, investigate quality issues, and recommend corrective actions to prevent recurrence. Their work is crucial in maintaining product safety, consistency, and compliance across various industries, such as manufacturing, pharmaceuticals, and food processing.
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Quality Control Investigator jobs near you
Infographic showing various Quality Control Investigator job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

Quality Control (QC) Chemist

Cipla

Fall River, MA • On-site

$65K - $105K/yr

Full-time

Re-posted 21 days ago

Job description

Quality Control (QC) Chemist - Inhalation Products (MDI Focus)

Location: Fall River, MA (On-site)
Schedule: 8:30 AM - 5:00 PM (flex based on production/testing needs)
Salary: $65,000 - $105,000 (based on expertise, especially inhalation experience)

  Bring Precision to Every Breath

Step into a critical role where science meets patient impact. As a QC Chemist specializing in inhalation products, you'll play a vital role in ensuring the safety, quality, and performance of metered dose inhalers (MDIs) and related dosage forms that patients rely on every day.

This is not your average QC role-here, you'll work on complex aerosol and particle-based delivery systems, applying advanced analytical techniques to confirm product integrity and regulatory compliance in a highly controlled cGMP environment.

  What You'll Do

Analytical Testing & Expertise

  • Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems)
  • Evaluate critical quality attributes (CQA) such as particle size distribution, spray pattern, plume geometry, and dose uniformity
  • Operate and maintain advanced instrumentation:
    • Gas Chromatography (GC)
    • Particle Size Analyzers (e.g., laser diffraction, cascade impaction)
    • ICP (trace elemental analysis)
  • Execute specialized inhalation testing protocols including propellant-based system assessments

Material & Product Understanding

  • Apply working knowledge of raw materials, propellants, excipients, and canister/valve systems specific to aerosol delivery
  • Support testing across multiple dosage forms (solid oral, liquids, injectables, topical, and inhalation platforms)

Data Integrity & Investigations

  • Ensure strict adherence to cGMP, data integrity standards, and ALCOA principles
  • Investigate OOS, deviations, and atypical results, contributing to root cause analysis and corrective actions

Documentation & Compliance

  • Maintain accurate, audit-ready documentation aligned with FDA and regulatory expectations
  • Follow and continuously improve SOPs in a structured QC environment
  What Makes You a Strong Candidate

Education & Technical Background

  • Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or Physics (highly preferred fields aligned with role expectations)
  • Strong foundation in analytical techniques and data interpretation

Industry Experience

  • Proven experience in a pharmaceutical QC environment (required)
  • Hands-on exposure to multiple dosage forms, especially:
    • Tablets/Capsules
    • Liquid formulations
    • Injectables
    • Topicals
    • MDI/DPI inhalation products (highly preferred)

Functional Expertise

  • Experience specifically in Quality Control roles (primary function)
  • Comfortable working in a fully onsite, regulated lab environment with fixed schedules and SOP-driven workflows
  • Strong communication skills and ability to interpret, document, and present scientific findings
  Work Environment
  • Operate in a state-of-the-art cGMP laboratory handling solvents, powders, and aerosol systems
  • Required use of PPE: lab coats, safety glasses, respirators, etc.
  • May include shift flexibility (day/evening/night) and occasional weekends based on production demands
  Physical Requirements
  • Stand/walk for extended periods (~75% of shift)
  • Lift up to 10 kg as needed
  • Perform detailed lab work requiring precision and focus
  Why This Role Stands Out

Inhalation Expertise - Work on advanced drug delivery systems that directly impact respiratory health
Technical Depth - Go beyond routine testing into specialized aerosol science and complex analytics
Career Growth - Build niche expertise in a high-demand domain within pharmaceuticals
Quality at the Core - Be a trusted gatekeeper ensuring every product meets the highest standards

  Important Notes
  • This is a fully onsite role (no remote or hybrid options)
  • Candidates must be authorized to work in the U.S. (no sponsorship available)

GLOBAL COMPANY

Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies.  Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare.  The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future.  Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)

About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.


EEO Statement

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.


  About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.  

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