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Internship Pharmaceutical Quality Control Jobs in Indiana

Orano

Quality Control Supervisor

Brownsburg, IN · On-site

At least 5 years of experience in pharmaceutical quality control, analytical development, or a related GMP laboratory function. * At least 1 year of experience as a laboratory supervisor, team lead ...

True Rx

Quality Control Specialist

Washington, IN · On-site

Quality Control Specialist Wanted at True Rx Health Strategists! Are you passionate about ensuring ... Our team of pharmacists and strategists delivers proven programs that find maximum savings and ...

Novartis

Supervisor, QC Chemistry

Indianapolis, IN

$88K - $132K/yr

Minimum of 5 years of relevant experience in the pharmaceutical, biologics, medical device, or ... (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological ...

Tate & Lyle

QC Lab Supervisor

Lafayette, IN

$71K - $95K/yr

Position Summary We are seeking an experienced and detail-oriented QC Lab Supervisor to lead daily ... Experience in food, beverage, ingredient, pharmaceutical, or other regulated manufacturing ...

Tate & Lyle

QC Lab Supervisor

Lafayette, IN · On-site

$71K - $95K/yr

Position Summary We are seeking an experienced and detail-oriented QC Lab Supervisor to lead daily ... Experience in food, beverage, ingredient, pharmaceutical, or other regulated manufacturing ...

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Internship Pharmaceutical Quality Control information

What is an internship in pharmaceutical quality control?

An Internship in Pharmaceutical Quality Control is a temporary training position where students or recent graduates gain practical experience in ensuring the quality and safety of pharmaceutical products. Interns typically work in laboratory settings, assisting with sample analysis, documentation, equipment calibration, and compliance with regulatory standards. This role helps interns develop key skills in laboratory techniques, data analysis, and understanding of Good Manufacturing Practices (GMP). It is a valuable opportunity for those considering a career in the pharmaceutical or biotechnology industries.

What are the typical responsibilities of an internship in pharmaceutical quality control?

As a Pharmaceutical Quality Control intern, you can expect to assist with routine laboratory testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory standards. Responsibilities often include preparing chemical reagents, performing analytical techniques (such as HPLC or spectroscopy) under supervision, recording and analyzing data, and maintaining lab equipment. Interns also learn proper documentation practices and may support investigations of deviations or out-of-specification results. This hands-on experience provides insight into the strict quality standards and teamwork required in the pharmaceutical industry.

What are the key skills and qualifications needed for an internship in pharmaceutical quality control?

To excel in a Pharmaceutical Quality Control internship, you need a solid understanding of chemistry, laboratory procedures, and basic GMP regulations, often gained through relevant coursework or a degree in pharmacy, chemistry, or a related field. Familiarity with analytical instruments like HPLC, GC, and software for data analysis is highly valued. Attention to detail, strong organizational skills, and effective communication set candidates apart in this environment. These skills ensure the accuracy and reliability of product testing, which is critical for maintaining safety, regulatory compliance, and product quality.

What is the difference between Internship Pharmaceutical Quality Control vs Pharmaceutical Quality Control Analyst?

AspectInternship Pharmaceutical Quality ControlPharmaceutical Quality Control Analyst
QualificationsEnrolled in or recent graduate of related degreeBachelor's degree in pharmacy, chemistry, or related field
Work EnvironmentTraining-focused, supervised lab settingFull-time professional lab environment
ResponsibilitiesAssisting with tests, learning proceduresPerforming quality tests, data analysis

Internship Pharmaceutical Quality Control roles are entry-level positions designed for students or recent graduates to gain industry experience. In contrast, Pharmaceutical Quality Control Analysts are full-time professionals responsible for executing quality tests and ensuring product compliance. The internship provides foundational exposure, while the analyst role involves independent work and responsibility.

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

The most popular types of Pharmaceutical Quality Control jobs in Indiana are:

What are popular job titles related to Internship Pharmaceutical Quality Control jobs in Indiana?

For Internship Pharmaceutical Quality Control jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Internship Pharmaceutical Quality Control jobs in Indiana look for?

The top searched job categories for Internship Pharmaceutical Quality Control jobs in Indiana are:

What cities in Indiana are hiring for Internship Pharmaceutical Quality Control jobs?

Cities in Indiana with the most Internship Pharmaceutical Quality Control job openings:

Internship Pharmaceutical Quality Control jobs near you
Infographic showing various Internship Pharmaceutical Quality Control job openings in Indiana as of August 2026, with employment types broken down into 73% Full Time, and 27% Contract. Highlights an 100% In-person job distribution.

Quality Control Supervisor

Orano

Brownsburg, IN • On-site

Full-time

Posted 26 days ago

Job description

Description
Orano Med, a subsidiary of Orano USA, is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the extraction and purification of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative Pb-212-based treatments which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells.
With a solid portfolio of development projects covering a diverse range of biological molecules capable of recognizing and targeting various forms of cancerous tumors, and a reliable supply chain for Pb-212, Orano Med aims to become a leader in targeted alpha therapies, in particular addressing needs of patients currently without effective therapeutic solutions among the existing approaches.
Position Summary
This is a working supervisor role. The individual is expected to learn, remain proficient in, and provide hands-on support for all assigned test methods, laboratory processes, and documentation practices. The Supervisor will set daily priorities, maintain a strong laboratory presence, and make timely operational and technical decisions.
The Supervisor will serve as a technical subject-matter expert and people leader. Responsibilities include analyst training, performance management, conflict resolution, laboratory investigations, and cross-functional communication. Success requires sound scientific judgment, strong technical writing and verbal communication, and calm decision-making under time-sensitive conditions.
Setup & Development Phase
  • Learn, perform, and maintain proficiency in all analytical test methods, laboratory processes, and controlled documentation practices within the assigned area.
  • Support analytical method development, optimization, qualification, validation, transfer, and lifecycle activities.
  • Establish training plans, qualification requirements, testing workflows, and clear expectations for compliant laboratory execution.
  • Support laboratory commissioning, instrument qualification, method readiness, staffing readiness, and analyst training.
  • Author and review protocols, reports, standard operating procedures, specifications, investigations, and other technical documents.
  • Provide scientific and operational input during process development, technology transfer, validation, and regulatory submission activities.

Production Phase
Top Priority: 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 testing priorities are clearly understood.
  • Maintain hands-on capability and perform or directly support routine test methods when needed to protect testing timelines and product release.
  • Serve as the primary technical subject-matter expert for analytical methods, laboratory investigations, and complex technical issues.
  • Make timely laboratory decisions during testing and release, escalating significant quality, safety, or compliance risks appropriately.
  • Coordinate testing priorities with Manufacturing, Quality Assurance, Supply Chain, and other functions to meet production schedules.
  • Train, coach, and evaluate laboratory personnel; provide clear feedback, reinforce accountability, and resolve personnel conflicts promptly and fairly.
  • Maintain a visible leadership presence in the laboratory during critical testing, troubleshooting, and release operations.
  • Review analytical data, laboratory records, calculations, and results for accuracy, completeness, scientific validity, and compliance.
  • Lead laboratory investigations and corrective actions, and support inspections, audits, deviations, change controls, and CAPA activities.

Continuous Improvement
  • Evaluate method performance, laboratory trends, deviations, recurring issues, and workload data to identify improvement opportunities.
  • Lead root-cause analysis and ensure corrective actions address technical, procedural, and organizational causes.
  • Improve laboratory workflows, training systems, documentation quality, and inspection readiness while maintaining cGMP compliance.
  • Promote knowledge sharing, technical development, effective communication, and cross-functional collaboration.

Location: On-site 100%
This position may receive other responsibilities as needed.
Requirements
Qualifications
Education
Bachelor's degree in chemistry, analytical chemistry, pharmaceutical sciences, radiochemistry, or a related scientific discipline is required. A Master's degree is preferred.
Experience
  • At least 5 years of experience in pharmaceutical quality control, analytical development, or a related GMP laboratory function.
  • At least 1 year of experience as a laboratory supervisor, team lead, or technical lead with responsibility for directing personnel and work.
  • Direct experience supporting radiopharmaceutical drug testing is strongly preferred.
  • Strong knowledge of analytical method execution, qualification, validation, transfer, troubleshooting, and lifecycle management.
  • Experience in a GMP-regulated environment supporting clinical or commercial manufacturing.
  • Hands-on experience with techniques such as HPLC, GC, gamma spectroscopy, radio-TLC, dose calibrators, and related instrumentation.
  • Demonstrated technical writing, verbal communication, decision-making, coaching, and personnel conflict-resolution skills.

Skills
  • Strong laboratory presence, safety awareness, and hands-on technical leadership
  • Technical subject-matter expertise, scientific troubleshooting, and data review
  • Sound decision-making under time-critical conditions
  • Clear technical writing and effective verbal communication

  • Coaching, performance feedback, accountability, and personnel conflict resolution
  • Organization, prioritization, attention to detail, and urgency while maintaining cGMP standards

Other
  • Travel <10>
  • Lift 50 lbs.

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