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Quality Control Professional Jobs in Massachusetts

Cipla

Quality Control (QC) Chemist

Fall River, MA

$65K - $105K/yr

Quality Control (QC) Chemist - Inhalation Products (MDI Focus) Location: Fall River, MA (On-site ... We are trusted by healthcare professionals and patients across geographies. Over the last eight ...

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 ... We are trusted by healthcare professionals and patients across geographies. Over the last eight ...

Cipla

$65K - $105K/yr

Quality Control (QC) Chemist - Inhalation Products (MDI Focus) Location: Fall River, MA (On-site ... We are trusted by healthcare professionals and patients across geographies. Over the last eight ...

MassHousing

Quality Control Specialist

Boston, MA · On-site

$15K/yr

Quality Control Specialist Organization: MassHousing Location: One Beacon Street, Boston, MA 02108 ... professionals, this might be the job for you! Interested candidates should send a letter of ...

Northeast Paving

Quality Control Technician

Northfield, MA · On-site

$17.50 - $22.50/hr

A Quality Control Technician typically performs a wide variety of tasks, transferring from one task ... Keep informed of professional and technical developments of new specifications to maintain and ...

TransMedics

Manager Quality Control

Andover, MA

Ensure the Quality Control department complies with 21CFR820, ISO 13485, MDSAP and MDR ... Excellent interpersonal skills demonstrating the ability to work with others in a professional ...

TransMedics

Manager Quality Control

Andover, MA · On-site

Ensure the Quality Control department complies with 21CFR820, ISO 13485, MDSAP and MDR ... Excellent interpersonal skills demonstrating the ability to work with others in a professional ...

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

Develop, mentor, and retain a high-performing QC organization, fostering a culture of accountability, collaboration, and continuous professional development. * Manage departmental budgets, capital ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210 - $220/hr

We are seeking an experienced professional to serve as Director of QC, supporting release, characterization, and environmental monitoring (EM) testing for cellular drug products manufactured ...

Integrated Resources INC

QC Microbiologist

Andover, MA

$25.75 - $34/hr

We've stayed true to our focus of finding qualified and experienced professionals in our specialty ... Position 1: This role will be responsible for the review of GMP documentation respective to QC ...

Kelly Services

Quality Control Inspector

Billerica, MA

$28 - $30/hr

We at Kelly ® hear you, and we're here for you! We're seeking a Quality Control Inspector I to ... Kelly ® Professional & Industrial recruiters are focused on only offering opportunities with ...

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Quality Control Professional information

What is the difference between Quality Control Professional vs Quality Assurance Technician?

AspectQuality Control ProfessionalQuality Assurance Technician
CertificationsISO 9001, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentManufacturing, production lines, labsManufacturing, labs, inspection facilities
Primary FocusInspecting products, identifying defectsDeveloping and implementing quality processes
Employer UsageManufacturers, production companiesManufacturers, quality departments

Both roles focus on quality but differ in scope. The Quality Control Professional primarily inspects products and detects defects, while the Quality Assurance Technician develops processes to prevent defects. Understanding these differences helps employers and job seekers target the right skills and certifications for each role.

Is quality control professional a good career?

A quality control professional plays a key role in ensuring products and services meet safety and quality standards, often requiring attention to detail and knowledge of industry regulations. The field offers opportunities for advancement, certifications, and employment in various industries such as manufacturing, healthcare, and technology. Job stability and demand are generally strong, especially with experience and specialized skills.

What is a career in quality control professional?

A career as a quality control professional involves inspecting products, processes, or services to ensure they meet specified standards and quality requirements. This role often requires attention to detail, knowledge of industry standards, and familiarity with testing tools or inspection techniques. Quality control professionals work in manufacturing, healthcare, food production, and other industries to maintain product safety and compliance.

What are the most commonly searched types of Quality Control jobs in Massachusetts?

The most popular types of Quality Control jobs in Massachusetts are:

Quality Control Professional jobs near you
Infographic showing various Quality Control Professional job openings in Massachusetts as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% In-person, and 9% Remote job distribution.

Quality Control (QC) Chemist

Cipla

Fall River, MA

$65K - $105K/yr

Full-time

Re-posted 3 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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