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Quality Control Chemist Jobs in Indiana (NOW HIRING)

The QC Chemist is responsible for performing tasks associated with release testing and reviewing laboratory data. Communicating with and supporting internal & external partners of the Quality Control ...

Quality Control Chemist Summary: INCOG is seeking a Quality Control (QC) Chemist with a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment ...

JOIN A TOP WORKPLACE - QC Chemist The primary purpose of this position is to perform required quality control analysis of incoming, manufactured, and outgoing material. Ensure all Quality Assurance ...

JOIN A TOP WORKPLACE - QC Chemist The primary purpose of this position is to perform required quality control analysis of incoming, manufactured, and outgoing material. Ensure all Quality Assurance ...

JOIN A TOP WORKPLACE - QC Chemist The primary purpose of this position is to perform required quality control analysis of incoming, manufactured, and outgoing material. Ensure all Quality Assurance ...

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Quality Control Chemist information

See Indiana salary details

$16

$30

$43

How much do quality control chemist jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for quality control chemist in Indiana is $30.06, according to ZipRecruiter salary data. Most workers in this role earn between $24.47 and $34.76 per hour, depending on experience, location, and employer.

What are Quality Control Chemists?

Quality Control Chemists are professionals who analyze and test materials and products to ensure they meet required standards and specifications. Their primary responsibility is to conduct laboratory tests on raw materials, in-process samples, and finished products using various chemical and analytical techniques. They document their findings, maintain laboratory equipment, and collaborate with other departments to resolve quality issues. Quality Control Chemists play a vital role in industries such as pharmaceuticals, food and beverage, and manufacturing to ensure product safety and compliance with regulations.

Where do QC chemists work?

Quality Control Chemists typically work in laboratories within manufacturing facilities, pharmaceutical companies, food production plants, or chemical processing plants. They perform testing and analysis of products, often using specialized equipment, and may work standard daytime shifts or in environments requiring strict safety protocols.

What does a quality control chemist do?

A quality control chemist tests and analyzes raw materials, in-process samples, and finished products to ensure they meet quality standards and specifications. They use laboratory equipment and techniques, such as chromatography and spectroscopy, and often follow strict protocols and documentation procedures to maintain product consistency and safety.

What is the highest paying chemist job?

Senior or specialized roles such as Pharmaceutical Chemist, Chemical Research Director, or Quality Control Manager tend to be the highest paying positions for chemists, often earning six-figure salaries. These roles typically require advanced education, extensive experience, and leadership skills in the industry.

How much do QC chemists make in the US?

The average salary for a Quality Control Chemist in the US is around $55,000 to $70,000 per year, depending on experience, education, and location. Entry-level positions typically start lower, while experienced chemists with specialized skills or certifications can earn higher salaries. Many QC chemists also receive benefits such as health insurance and paid time off.

What are the key skills and qualifications needed to thrive as a Quality Control Chemist, and why are they important?

To thrive as a Quality Control Chemist, you need a solid background in chemistry, analytical techniques, and a relevant bachelor's degree in chemistry or a related field. Familiarity with laboratory instruments like HPLC, GC, and spectrophotometers, as well as knowledge of regulatory standards such as GMP or ISO, is typically required. Attention to detail, problem-solving ability, and strong organizational skills are crucial soft skills for this role. These competencies ensure the accuracy, reliability, and compliance of product testing, which are vital for product safety and quality assurance.

What Is a Quality Control Chemist?

A quality control chemist (QC chemist) is a specific type of laboratory chemist, whose primary duties are to measure and test lab materials and products according to industry-specific standard procedures. Jobs are typically in the pharmaceutical or manufacturing fields. As a QC chemist, you assure adherence to all federal regulations and safety procedures. In addition to performing rigorous quality assurance of samples, some QC chemists are responsible for calibrating and performing maintenance on lab equipment. Relevant qualifications for this career include a bachelor’s degree in chemistry, experience in a chemistry lab setting, and skills like attention to detail and the ability to multitask.

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

AspectQuality Control ChemistQuality Assurance Technician
CredentialsBachelor's in Chemistry or related field; certifications like CQE beneficialBachelor's in Chemistry, Quality Management, or related; certifications like CQTA helpful
Work EnvironmentLaboratory setting, testing raw materials, in-process, and finished productsManufacturing or production environment, focusing on process compliance and documentation
Employer & IndustryPharmaceutical, food, cosmetics, chemical industriesManufacturing, pharmaceutical, food, and beverage industries

While both roles ensure product quality, the Quality Control Chemist primarily conducts laboratory testing and analysis, whereas the Quality Assurance Technician focuses on process monitoring and compliance to prevent defects. Both positions are essential for maintaining product standards in manufacturing industries.

What are some common challenges faced by Quality Control Chemists in maintaining consistent testing standards across different production batches?

Quality Control Chemists often encounter challenges in ensuring consistency due to variations in raw materials, equipment calibration, and environmental conditions. Addressing these issues requires diligent documentation, regular equipment maintenance, and strict adherence to standard operating procedures. Effective communication with production and R&D teams is also essential to quickly resolve discrepancies and implement corrective actions, ensuring that all products meet quality and regulatory standards.
What are popular job titles related to Quality Control Chemist jobs in Indiana? For Quality Control Chemist jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Quality Control Chemist jobs in Indiana look for? The top searched job categories for Quality Control Chemist jobs in Indiana are:
What cities in Indiana are hiring for Quality Control Chemist jobs? Cities in Indiana with the most Quality Control Chemist job openings:
What are popular job titles related to Quality Control Chemist jobs in IN? For Quality Control Chemist jobs in IN, the most frequently searched job titles are:
Infographic showing various Quality Control Chemist job openings in Indiana as of July 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 100% In-person job distribution, with an average salary of $62,530 per year, or $30.1 per hour.

$97K - $146K/yr

Full-time

Re-posted 20 days ago


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Job description

Job Description Summary

Location: Indianapolis, IN #LI-Onsite
About this role:
The QC Chemist is responsible for performing tasks associated with release testing and reviewing laboratory data. Communicating with and supporting internal & external partners of the Quality Control organization is also required.


Job Description

Major accountabilities:

  • Provide support to peers within the Quality Assurance, Quality Control and AS&T teams.
  • On-time and GMP-compliant release of dosage forms
  • Support Quality Control and AS&T as a valued business partner, with a culture of safety, quality,
  • delivery to patients, cost, compliance, and data integrity.

  • Author, review and support procedures, investigations, corrective and preventive actions, change
  • controls, complaints, and training as it relates to quality control testing.

  • Ensure that QC testing is properly conducted and documented for all performed activities, with
  • emphasis on Data Integrity. Evaluate and approve QC records as required.

  • Provide oversight and monitoring of quality control KPIs and programs.
  • Perform QC related validations, transfers, improvements, investigations related activities (deviations, OOS, OOE, OOT, CAPAs, trending), and Change Control systems.
  • Prepare and participate in health authorities’ inspections and internal audits of QC. Ensure quality control area is inspection ready.

Essential Requirements

  • BSc in Chemistry or relevant scientific
  • 3+ years of experience in a GMP quality control environment
  • Strong HPLC experience a must
  • General HSE Knowledge
  • Knowledge of GMP Manufacturing Process Execution
  • Quality Control (QC) Testing
  • Quality Control Sampling
  • Dealing With Ambiguity.
  • GMP Procedures
  • Quality Control (Qc) Testing.
  • Quality Standards.
  • Self Awareness.
  • Technological Expertise.
  • Technological Intelligence.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$97,600.00 - $146,400.00


Skills Desired

Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

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