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Quality Control Chemistry Intern Jobs in Indiana

Novartis

Supervisor, QC Chemistry

Indianapolis, IN · On-site

$88K - $132K/yr

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 ...

INCOG

QC Chemist, 3rd Shift

Fishers, IN

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 ...

Novartis

QC Chemist

Indianapolis, IN · On-site

$97K - $146K/yr

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 ...

INCOG

QC Sample Management Technician, 2nd Shift

Fishers, IN · On-site

$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 ...

Orano

Quality Control Supervisor

Brownsburg, IN · On-site

Execute and supervise QC testing for batch release within hours of production Routine Functions - QC * Direct daily QC Chemistry laboratory operations, assign work, balance staffing, and ensure ...

SpectronRx

QC Specialist

Indianapolis, IN · On-site

$29 - $34/hr

Quality Control Specialist COMPANY OVERVIEW SpectronRx is a growing Contract Development and ... Wet Chemistry testing including pH, Osmolality, Immunoreactivity Fraction (IRF) testing * Prepare ...

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Quality Control Chemistry Intern information

What does a quality control chemistry intern do?

A Quality Control Chemistry Intern assists in testing and analyzing raw materials, in-process samples, and finished products to ensure they meet quality and safety standards. They work under the supervision of experienced chemists, using various laboratory instruments and techniques such as titration, spectroscopy, and chromatography. Interns are also responsible for maintaining accurate records of test results, following strict lab procedures, and helping to troubleshoot issues with equipment or processes. This role provides valuable hands-on experience in a laboratory environment and helps interns develop skills important for a career in quality control and analytical chemistry.

What is the difference between Quality Control Chemistry Intern vs Quality Control Chemist?

AspectQuality Control Chemistry InternQuality Control Chemist
CredentialsEnrolled in or recent graduate of a chemistry or related programBachelor's degree in chemistry or related field, often with experience
Work EnvironmentLaboratory, internship setting, supervisedLaboratory, production, or quality assurance departments, more autonomous
Employer & Industry UsageInternship programs in pharmaceutical, biotech, or manufacturing companiesFull-time roles in similar industries, responsible for quality testing

The main difference is that a Quality Control Chemistry Intern is typically a student or recent graduate gaining hands-on experience under supervision, while a Quality Control Chemist is a full-time professional responsible for routine testing and quality assurance tasks. Interns focus on learning, whereas Chemists perform ongoing quality control duties independently.

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

To thrive as a Quality Control Chemistry Intern, you need a solid understanding of analytical chemistry, laboratory safety, and experience with standard laboratory procedures, typically gained through coursework in chemistry or a related science. Familiarity with analytical instruments such as HPLC, GC, and spectrophotometers, as well as proficiency in using laboratory information management systems (LIMS), is often required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for accurately documenting data and collaborating with team members. These skills and qualities ensure precise testing, regulatory compliance, and support the overall quality assurance process in laboratory environments.

What types of projects or tasks can a quality control chemistry intern expect to work on during their internship?

As a Quality Control Chemistry Intern, you can expect to be involved in hands-on laboratory work such as preparing chemical solutions, conducting routine analytical tests like HPLC or titrations, and supporting the documentation of results in accordance with Good Laboratory Practices (GLP). You may also assist with equipment calibration, participate in investigations of out-of-specification results, and help maintain lab safety and cleanliness. This role often requires close collaboration with experienced chemists and quality assurance teams, offering valuable exposure to industry-standard procedures and teamwork within a regulated environment.

What cities in Indiana are hiring for Quality Control Chemistry Intern jobs?

Cities in Indiana with the most Quality Control Chemistry Intern job openings:

Quality Control Chemistry Intern jobs near you

Supervisor, QC Chemistry

Novartis

Indianapolis, IN • On-site

$88K - $132K/yr

Full-time

Re-posted 16 days ago

Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

64th of 86 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

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Benefits

Hours and flexibility

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