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Qc Laboratory Manager Jobs in Indiana (NOW HIRING)

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 ... Supervision of laboratory personnel. * Provide oversight for personnel work schedules as well as ...

ravagoamericas

Quality Control Technician

Greenwood, IN · On-site

$17.75 - $22.75/hr

All laboratory activities are to be conducted according to good laboratory practices (GLP) and ... Most possess good time management skills and be able to plan and execute daily functions with ...

ravagoamericas

Quality Control Technician

Greenwood, IN

$17.75 - $22.75/hr

All laboratory activities are to be conducted according to good laboratory practices (GLP) and ... Most possess good time management skills and be able to plan and execute daily functions with ...

INCOG

QC Sample Management Technician, 2nd Shift

Fishers, IN

$17.50 - $22.50/hr

The QC Sample Management Technician plays a critical role in maintaining data integrity, inspection readiness, and efficient laboratory operations by ensuring samples are handled in accordance with ...

New

Evonik Corporation

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

Evonik Corporation

The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross ... Demonstrated ability to independently manage laboratory investigations and technical projects.

Tate & Lyle

QC Lab Supervisor

Lafayette, IN

$71K - $95K/yr

Manage laboratory inventory and maintain adequate supplies to support operations. * Coordinate ... Quality Assurance or Quality Control experience within a manufacturing environment. * Strong ...

Ravago Americas

Quality Control Technician

Greenwood, IN · On-site

$17.75 - $22.75/hr

All laboratory activities are to be conducted according to good laboratory practices (GLP) and ... Most possess good time management skills and be able to plan and execute daily functions with ...

Tate & Lyle

QC Lab Supervisor

Lafayette, IN · On-site

$71K - $95K/yr

Manage laboratory inventory and maintain adequate supplies to support operations. * Coordinate ... Quality Assurance or Quality Control experience within a manufacturing environment. * Strong ...

Linde Group

QC Lab Technician

Indianapolis, IN · On-site

$17.75 - $22.50/hr

You will report and interpret data within the laboratory management system and communicate with production, QC Team lead and or other lab management as required * You will perform testing which ...

Linde

QC Lab Technician

Indianapolis, IN

$17.75 - $22.50/hr

You will report and interpret data within the laboratory management system and communicate with production, QC Team lead and or other lab management as required * You will perform testing which ...

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All JobsQc Laboratory JobsQc Laboratory Manager JobsQc Laboratory Manager Jobs in Indiana

Qc Laboratory Manager information

What is a QC Laboratory Manager?

A QC (Quality Control) Laboratory Manager oversees the daily operations of a quality control laboratory, ensuring that all testing procedures and results meet regulatory and company standards. They are responsible for supervising laboratory staff, developing and implementing quality control protocols, and maintaining compliance with health and safety regulations. QC Laboratory Managers also analyze test data, troubleshoot issues with equipment or procedures, and communicate findings with other departments to ensure product quality. Their role is crucial in industries like pharmaceuticals, food and beverage, and manufacturing, where product safety and quality are paramount.

What are the key skills and qualifications needed to thrive as a QC Laboratory Manager?

To thrive as a QC Laboratory Manager, you need a strong background in chemistry or biology, experience in laboratory operations, and a relevant degree, often supported by prior supervisory experience. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and industry-specific quality standards such as ISO 17025 is essential. Leadership, attention to detail, and effective communication are key soft skills that help manage teams and ensure regulatory compliance. These skills are crucial for maintaining high-quality standards, ensuring accurate test results, and leading laboratory teams efficiently.

What is the difference between Qc Laboratory Manager vs Qc Analyst?

AspectQc Laboratory ManagerQc Analyst
CredentialsBachelor's or higher in Chemistry, Biology, or related; often requires management experienceBachelor's in Chemistry, Biology, or related; certifications like ASQ are common
Work EnvironmentOversees laboratory operations, manages staff, ensures compliancePerforms testing, analyzes data, reports results
Industry UsageUsed in pharmaceutical, biotech, food, and manufacturing industriesCommonly employed in similar industries for quality testing

The Qc Laboratory Manager focuses on overseeing laboratory operations, managing staff, and ensuring compliance with regulations. In contrast, the Qc Analyst primarily conducts testing and analyzes quality data. Both roles require relevant scientific credentials and are integral to quality assurance in manufacturing and biotech sectors.

What are the main challenges a QC Laboratory Manager faces when leading a team in a fast-paced manufacturing environment?

A QC Laboratory Manager often navigates the challenge of balancing strict regulatory compliance with the need for efficient turnaround times. Managing a diverse team requires strong communication and training to ensure consistent testing and data integrity. Additionally, adapting to rapid changes in production schedules and troubleshooting equipment or process issues are frequent demands. Success in this role involves proactive planning, fostering a culture of continuous improvement, and effective cross-department collaboration.
What are popular job titles related to Qc Laboratory Manager jobs in Indiana? For Qc Laboratory Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Qc Laboratory Manager jobs in Indiana look for? The top searched job categories for Qc Laboratory Manager jobs in Indiana are:
Qc Laboratory Manager jobs near you
Infographic showing various Qc Laboratory Manager job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Supervisor, QC Chemistry

Novartis

Indianapolis, IN • On-site

$88K - $132K/yr

Full-time

Re-posted 9 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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