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Quality Control Analyst Jobs in Fishers, IN (NOW HIRING)

Orano

Quality Control Supervisor

Brownsburg, IN · On-site

Support analytical method development, optimization, qualification, validation, transfer, and ... Execute and supervise QC testing for batch release within hours of production Routine Functions ...

INCOG

QC Sample Management Technician, 2nd Shift

Fishers, IN

$17.50 - $22.50/hr

Communicate sample status, priorities, and issues to QC analysts, supervisors, and QC Technical Services as needed. Sample Retention and Disposition * Manage sample retention programs, including ...

New

ravagoamericas

Quality Control Technician

Greenwood, IN · On-site

$17.75 - $22.75/hr

The technician will conduct preliminary, in-process, and final analysis of materials that are used ... QC Supervisor in organizing and storing retain samples, and the disposal of laboratory waste and ...

Clayco

Quality Technician

Indianapolis, IN · On-site

$15.75 - $21.25/hr

... A/QC role. * Proficient in the use of software including Microsoft Office Suite. * Strong analytical and problem-solving skills with attention to detail. * Ability to walk a job site and climb ...

ravagoamericas

Quality Control Technician

Greenwood, IN

$17.75 - $22.75/hr

The technician will conduct preliminary, in-process, and final analysis of materials that are used ... QC Supervisor in organizing and storing retain samples, and the disposal of laboratory waste and ...

Clayco

Quality Manager

Indianapolis, IN · On-site

Deliver daily QC reports aligned with project quality standards. * Collaborate with the project ... Strong analytical and problem-solving skills with high attention to detail. * Ability to walk job ...

Ravago Americas

Quality Control Technician

Greenwood, IN · On-site

$17.75 - $22.75/hr

The technician will conduct preliminary, in-process, and final analysis of materials that are used ... QC Supervisor in organizing and storing retain samples, and the disposal of laboratory waste and ...

CARLISLE COMPANIES

Quality Control Technician

Greenfield, IN · On-site

$18 - $23/hr

Job Summary Ability to perform various quality control tests on products to verify that all ... Conduct root cause analysis regarding quality issues, identify and implement appropriate corrective ...

PinnaclePartners

QC Engineer

Indianapolis, IN · On-site

$90K - $100K/yr

Title: QC Engineer Comp: $90,000 - $120,000 Location: Indianapolis, IN Our client is seeking immediate assistance in identifying a candidate for a QC Engineer direct hire in Indianapolis, IN.

NFI Industries

Quality Control Checker

Whiteland, IN · On-site

Overview The Quality Control Checker is responsible for the accurate checking or counting of all ... Excellent analytical and mathematical skills * Excellent customer service skills * Able to work ...

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All JobsQuality Control Analyst JobsQuality Control Analyst Jobs in Fishers, IN

Quality Control Analyst information

See Fishers, IN salary details

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How much do quality control analyst jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for quality control analyst in Fishers, IN is $25.13, according to ZipRecruiter salary data. Most workers in this role earn between $20.77 and $27.93 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

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

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by quality control analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What is a quality control analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

Is a quality control analyst a good job?

A quality control analyst is a valuable role in industries such as manufacturing, pharmaceuticals, and food production, focusing on ensuring products meet quality standards through testing and inspection. The job typically requires attention to detail, knowledge of testing tools and procedures, and may involve certifications like Six Sigma or ISO standards. It offers stable employment with opportunities for advancement and skill development.
More about Quality Control Analyst jobs
What job categories do people searching Quality Control Analyst jobs in Fishers, IN look for? The top searched job categories for Quality Control Analyst jobs in Fishers, IN are:
What cities near Fishers, IN are hiring for Quality Control Analyst jobs? Cities near Fishers, IN with the most Quality Control Analyst job openings:
Quality Control Analyst jobs near you
Infographic showing various Quality Control Analyst job openings in Fishers, IN as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $52,277 per year, or $25.1 per hour.

Quality Control Supervisor

Orano

Brownsburg, IN • On-site

Full-time

Posted 9 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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