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Quality Control Chemist Jobs (NOW HIRING)

Novartis

QC Chemist

Indianapolis, IN

$97K - $146K/yr

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 ...

TekWissen LLC

Quality Control Chemist

High Point, NC · On-site

Quality Control Chemist Location: High Point, NC, 27265 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Summary: We are seeking a Quality Control Chemist / Associate Scientist to ...

Fujifilm

QC Chemist

Mesa, AZ · On-site

The Role The QC Chemist serves as a Quality Control Specialist responsible for analyzing semiconductor materials in support of product qualification and to support all Quality Control laboratory ...

Coast Southwest, Inc.

The Quality Control Chemist will be responsible for analyzing materials using a variety of instrumental and testing methods as part of the Coast Southwest Quality Control Laboratory Department.

GRIFOLS, S.A.

Quality Control Chemist

Los Angeles, CA · On-site

The QC Chemist is responsible for performing routine and non-routine chemical and biochemical assays on protein-based therapeutics and raw materials. Essential Job Duties: * Perform various QC / ...

Grifols

Quality Control Chemist

Los Angeles, CA · On-site

The QC Chemist is responsible for performing routine and non-routine chemical and biochemical assays on protein-based therapeutics and raw materials. Essential Job Duties: * Perform various QC / ...

RXinsider LTD.

Quality Control Chemist

Houston, TX · On-site

Position Summary The Quality Control Chemist is responsible for the review, approval, and maintenance of analytical chemistry documentation and quality records to ensure compliance with regulatory ...

Eagle

Quality Control Chemist

Houston, TX

Position Summary The Quality Control Chemist is responsible for the review, approval, and maintenance of analytical chemistry documentation and quality records to ensure compliance with regulatory ...

RXinsider LTD.

Position Summary The Quality Control Chemist is responsible for the review, approval, and maintenance of analytical chemistry documentation and quality records to ensure compliance with regulatory ...

Eagle

Quality Control Chemist

Houston, TX · On-site

Position Summary The Quality Control Chemist is responsible for the review, approval, and maintenance of analytical chemistry documentation and quality records to ensure compliance with regulatory ...

Us tech Solutions

Quality control chemist

Myerstown, PA · On-site

Quality control chemist- 2nd shift Duration: 12 Months Location: Myerstown, PA 17067 Description: The Raw Material testing team is responsible for Quality Control testing of APIs and excipients used ...

Hays

Quality Control Chemist II

Johns Creek, GA · On-site

This is an excellent opportunity for an experienced analytical chemist with a strong background in method validation, laboratory instrumentation, and quality control testing within a regulated ...

Chemence

Quality Control Chemist

Alpharetta, GA · On-site

Summary: QC Chemist personnel ensure that profitable, quality product is sold to the marketplace in compliance with the applicable ISO standards by the efficient, reproducible, and accurate analysis ...

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Quality Control Chemist information

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How much do quality control chemist jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for quality control chemist in the United States is $31.59, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $36.54 per hour, depending on experience, location, and employer.

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

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 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 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.

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Quality Control Chemist jobs near you
Infographic showing various Quality Control Chemist job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $65,713 per year, or $31.6 per hour.

QC Chemist

Indianapolis, IN

Novartis
Pharmaceutical and Medicine Manufacturing • 10K+ employees
Learn more about Novartisexternal

$97K - $146K/yr

Full-time

Re-posted 5 days ago

Key responsibilities

  • Perform tasks associated with release testing and review laboratory data to ensure GMP compliance.

  • Support quality control activities, including authoring, reviewing, and supporting procedures, investigations, and change controls.

  • Prepare for and participate in health authorities' inspections and internal audits of the QC area.

Novartis rating

7.8

Company rating: 7.8 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

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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