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Quality Control Chemistry Jobs in Indiana (NOW HIRING)

In this people management role, the QC Chemistry Supervisor works with the Quality Control team in supporting our efforts of RLT therapy. This role is responsible for the day-to-day oversight of the ...

Bachelor's Degree in Science (Chemistry or Biochemistry) * Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control ...

QC Chemistry Technician, 2nd Shift

Fishers, IN · On-site

$18.50 - $23.50/hr

Performs sample management activities for Quality Control Chemistry Laboratory including management of samples from clean utilities, components, raw materials, in-process samples, finished product ...

QC Chemistry Technician, 3rd Shift

Fishers, IN

$18.50 - $23.50/hr

Performs sample management activities for Quality Control Chemistry Laboratory including management of samples from clean utilities, components, raw materials, in-process samples, finished product ...

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 ...

Quality Control Chemist Location of the job: Hammond, IN (Union) Rotating Shift Hours: (1st week) 7 ... All other duties as assigned What You'll Need To Succeed * 4 year degree in Chemistry, Biology ...

QC Sample Management Technician

Fishers, IN

$17.50 - $22.50/hr

Coordinate sample distribution to QC Chemistry, QC Microbiology, and external testing laboratories as required. * Ensure samples are transferred, shipped, or staged in compliance with internal ...

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Quality Control Chemistry information

See Indiana salary details

$16

$30

$43

How much do quality control chemistry jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for quality control chemistry 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 is the difference between Quality Control Chemistry vs Quality Assurance Specialist?

AspectQuality Control ChemistryQuality Assurance Specialist
CertificationsOften requires a Bachelor's in Chemistry or related field, with certifications like ASQ CQE or similarSimilar certifications, with focus on process audits and compliance
Work EnvironmentLaboratory settings, testing labs, manufacturing plantsOffice-based, audits, documentation, and process review environments
Primary FocusTesting raw materials, in-process, and finished products for quality and complianceDeveloping, implementing, and maintaining quality systems and procedures
Industry UsageCommonly used in manufacturing, pharmaceuticals, and chemical industriesUsed across similar industries but with a broader focus on quality systems

While both roles aim to ensure product quality, Quality Control Chemistry focuses on laboratory testing and analysis, whereas Quality Assurance Specialists develop and oversee quality systems and processes to prevent defects.

What are some common challenges faced in a Quality Control Chemistry role, and how can they be addressed?

Quality Control Chemists often face challenges such as tight deadlines for product release, maintaining compliance with changing regulatory standards, and managing complex testing protocols. To address these, effective time management, continuous training on regulations, and strong attention to detail are essential. Additionally, collaborating with production and R&D teams helps resolve discrepancies quickly and ensures that quality standards are consistently met.

What is Quality Control Chemistry?

Quality Control Chemistry is a branch of chemistry focused on ensuring that products, especially in industries like pharmaceuticals, food, and manufacturing, meet quality and safety standards. Quality Control (QC) Chemists analyze raw materials, in-process samples, and finished products using a variety of analytical techniques to verify their composition and purity. Their work helps identify any deviations from regulatory or company standards, ensuring that products are safe and effective for consumers. QC Chemistry is crucial for compliance with government regulations and maintaining a company's reputation.

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 understanding of analytical chemistry, laboratory techniques, and a bachelor's degree in chemistry or a related field. Familiarity with instruments such as HPLC, GC, FTIR, and LIMS, as well as knowledge of GMP/GLP regulations, is typically required. Attention to detail, critical thinking, and effective communication are valuable soft skills that enhance accuracy and teamwork. These competencies are crucial for ensuring product quality, regulatory compliance, and reliable laboratory operations.
What are popular job titles related to Quality Control Chemistry jobs in Indiana? For Quality Control Chemistry jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Quality Control Chemistry jobs in Indiana look for? The top searched job categories for Quality Control Chemistry jobs in Indiana are:
What cities in Indiana are hiring for Quality Control Chemistry jobs? Cities in Indiana with the most Quality Control Chemistry job openings:
Supervisor, QC Chemistry

Supervisor, QC Chemistry

Novartis

Indianapolis, IN

$88K - $132K/yr

Full-time

Re-posted 20 days ago


Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

55th of 74 rated pharmaceutical


Job description

Job Description Summary

Location: Indianapolis, IN #LI-Onsite
About this role:
In this people management role, the QC Chemistry Supervisor works with the Quality Control team in supporting our efforts of RLT therapy. This role is responsible for the day-to-day oversight of the QC Chemistry team including raw material testing and final product testing.


Job Description

Key Responsibilities:

  • Supervision of laboratory personnel.
  • Provide oversight for personnel work schedules as well as for scheduling and completion of testing and documentation.
  • Provides oversight towards QC laboratory equipment maintenance.
  • Expertise in one or more of the following methodologies: HPLC/UPLC, wet chemistry, TLC, endotoxin, radionuclidic identity by half-life, environmental monitoring, sterility
  • Maintain the laboratory and laboratory procedures/processes in a constant state of inspection readiness.
  • Ensure personnel are appropriately trained and cross-trained.
  • Author, review, and approve technical documents.
  • Ensure trending reports are completed and approved within established timelines.
  • Support 5S and Lean Laboratory implementation and sustainability.
  • Provide support of laboratory related manufacturing investigations, CAPAs, and change controls.
  • Ensure safety requirements are met and maintained.
  • Perform other job duties as assigned.
  • Design and execute method transfers/qualifications/validations based on Regulatory guidelines and industry best practices.
  • Collaborate with other groups to drive project success.
  • Troubleshoot method challenges.
  • Manage method development and optimization activities as needed.

Essential Requirements:

  • BS or MS in Biology, Chemistry, Microbiology or other related science.
  • Minimum of 5 years of relevant experience in the pharmaceutical, biologics, medical device, or advanced therapy medicinal products industry.
  • Previous supervisory experience is recommended but not required.
  • Working knowledge of aseptic manufacturing, cGMPs, GLPs and applicable compendial and regulatory guidelines (e.g. FDA, EP, JP)
  • Thorough knowledge of analytical and microbiological test methods.
  • Experience with LIMS.

Commitment to Diversity and Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.


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

$88,000.00 - $132,000.00


Skills Desired

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

What Novartis employees say

Pay

Benefits

Hours and flexibility

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