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Quality Control In Jobs in Westfield, IN (NOW HIRING)

Orano

Quality Control Supervisor

Brownsburg, IN · On-site

Based on its unique expertise in the extraction and purification of lead-212 (Pb-212) and ... Execute and supervise QC testing for batch release within hours of production Routine Functions ...

Faith Technologies

QC Electrician

Lebanon, IN

Cares about leading the way in construction, engineering, manufacturing and renewable energy. Cares ... The Quality Control Electrician is responsible for delivery of quality control services including ...

Faithtechnologies

QC Electrician

Lebanon, IN

Cares about leading the way in construction, engineering, manufacturing and renewable energy. Cares ... The Quality Control Electrician is responsible for delivery of quality control services including ...

Kelly Services

Quality Control Specialist

Indianapolis, IN

$24.55/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Indianapolis, IN Pay Rate: $24.55/hour Shift: Sunday through Thursday, 11:00pm to 7:30am (3rd Shift) Summary Kelly Services is hiring a Temporary Quality Control Inspectors will perform component ...

Eurofins Scientific

QC Specialist

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The QC Specialist will also participate in second person verification (SPV ) of analytical data, laboratory investigations, equipment calibrations, and maintenance by executing well-defined protocols ...

Eurofins

QC Specialist

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The QC Specialist will also participate in second person verification (SPV ) of analytical data, laboratory investigations, equipment calibrations, and maintenance by executing well-defined protocols ...

Criticalarccx

QA/QC Engineer

Indianapolis, IN · On-site

$90 - $190/hr

CriticalArc is seeking qualified individuals for a QA/QC Engineer position to support a mission-critical project in Indianapolis, Indiana. The base salary range for this position is $90,000 to $190 ...

New

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 ...

IMI

Aggregate Quality Control Technician

Noblesville, IN

$17.50 - $22.50/hr

The job of a Qualified Technician is to test concrete and materials used for producing concrete in ... Perform testing procedures and report those results to the QC Manager * Demonstrate a commitment to ...

INCOG

QC Equipment Coordinator

Fishers, IN · On-site

$18.50 - $25.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Quality Control Equipment Coordinator Summary The Quality Control Equipment Coordinator is essential in assisting the QC team with qualifying, calibrating, and maintaining quality control instruments ...

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Showing results 21-40

All JobsQuality Control In JobsQuality Control In Jobs in Westfield, IN

Quality Control In information

See Westfield, IN salary details

$29.3K

$78K

$124.2K

How much do quality control in jobs pay per year?

As of Aug 19, 2026, the average yearly pay for quality control in in Westfield, IN is $78,001.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $95,900.00 per year, depending on experience, location, and employer.

What is the difference between Quality Control In vs Quality Control Inspector?

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

What does a quality control in job do?

A quality control in job involves inspecting products or services to ensure they meet specified standards and quality requirements. It includes tasks such as testing, measuring, and reviewing processes, often using tools like checklists or testing equipment, to identify defects and ensure customer satisfaction.

What cities near Westfield, IN are hiring for Quality Control In jobs?

Cities near Westfield, IN with the most Quality Control In job openings:

Quality Control In jobs near you
Infographic showing various Quality Control In job openings in Westfield, IN as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $78,001 per year, or $37.5 per hour.

Quality Control Supervisor

Orano

Brownsburg, IN • On-site

Full-time

Posted 21 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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