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Glp Jobs in Indiana (NOW HIRING)

Lead Internal Auditor, GLP/GCP

Indianapolis, IN ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

Lead Internal Auditor, GLP/GCP

Indianapolis, IN

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

Quality Auditor - GLP/GCP

Indianapolis, IN ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Labcorp is seeking a Quality Auditor, GLP/GCP to join our team in Indianapolis, IN Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Quality Auditor plays a pivotal role as part ...

Quality Auditor - GLP/GCP

Indianapolis, IN

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Labcorp is seeking a Quality Auditor, GLP/GCP to join our team in Indianapolis, IN Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Quality Auditor plays a pivotal role as part ...

Provide sponsor oversight for outsourced GLP studies, including protocol and final report reviews, and collaborate with study teams to ensure regulatory compliance. * Issue audit reports, QA ...

Licensing Consultant

Indianapolis, IN ยท On-site

$110 - $160/hr

As a Licensing Consultant on the Global Licensing Programs (GLP) team, you serve as a critical strategic advisor and escalation point within the Salesforce Foundations ecosystem--spanning Tableau, CR ...

Licensing Consultant

Indianapolis, IN

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Licensing Consultant on the Global Licensing Programs (GLP) team, you serve as a critical strategic advisor and escalation point within the Salesforce Foundations ecosystem-spanning Tableau, CRM ...

Licensing Consultant

Indianapolis, IN ยท On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a Licensing Consultant on the Global Licensing Programs (GLP) team, you serve as a critical strategic advisor and escalation point within the Salesforce Foundations ecosystem-spanning Tableau, CRM ...

Veterinary Anatomic Pathologist

Indianapolis, IN ยท On-site

$169K - $312K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience in pathology peer review of data from GLP nonclinical toxicity studies * Experience in the interpretation and/or reporting of clinical pathology data from nonclinical toxicity studies

R&D Formulation Scientist

Columbus, IN ยท On-site

$27 - $30/hr

Adhere to all safety guidelines, SOPs, and Good Laboratory Practices (GLP). Qualifications * Bachelor's degree in Microbiology, Biology, Chemistry, Pharmaceutical Sciences, or a related scientific ...

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Glp information

See Indiana salary details

$5

$21

$61

How much do glp jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for glp in Indiana is $21.79, according to ZipRecruiter salary data. Most workers in this role earn between $13.70 and $18.32 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals working in GLP (Good Laboratory Practice) roles, and how can they be addressed?

Professionals in GLP roles often encounter challenges such as maintaining meticulous documentation, ensuring strict protocol adherence, and staying updated with evolving regulatory standards. These responsibilities require strong attention to detail and effective time management. Collaboration with cross-functional teams, such as quality assurance and laboratory staff, is essential to ensure compliance and data integrity. Regular training and open communication channels can help address these challenges and support a smooth workflow.

What is the difference between Glp vs Pharmacist?

AspectGlpPharmacist
Required CredentialsCertification in Good Laboratory Practice (GLP) standardsDoctor of Pharmacy (PharmD) or equivalent, licensure
Work EnvironmentLaboratories, research facilitiesPharmacies, hospitals, clinics
Industry UsageRegulatory compliance, research oversightMedication dispensing, patient care
Common Search/ComparisonGLP vs PharmacistPharmacist roles, responsibilities

GLP professionals focus on ensuring laboratory compliance with regulatory standards in research settings, while pharmacists are healthcare providers responsible for dispensing medications and advising patients. Both roles require specialized knowledge but serve different functions within the healthcare and research industries.

What is a GLP (Good Laboratory Practice) professional?

GLP professionals are individuals who ensure that laboratory studies are conducted in accordance with Good Laboratory Practice regulations. These standards are designed to ensure the quality, reliability, and integrity of non-clinical laboratory studies, particularly those related to the safety of pharmaceuticals, chemicals, and other products. GLP professionals may work in various roles, such as quality assurance, study direction, data management, or laboratory operations. Their responsibilities include maintaining documentation, overseeing compliance, and supporting audits or inspections. By adhering to GLP guidelines, they help ensure that data generated in the lab are credible and accepted by regulatory agencies.

What are the key skills and qualifications needed to thrive as a GLP (Good Laboratory Practice) specialist, and why are they important?

To thrive as a GLP Specialist, you need a solid background in laboratory sciences, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in GLP environments. Familiarity with laboratory information management systems (LIMS), audit processes, and documentation standards is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure data integrity, regulatory compliance, and the smooth operation of laboratory processes subject to strict guidelines.

What are popular job titles related to Glp jobs in Indiana?

For Glp jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Glp jobs in Indiana look for?

The top searched job categories for Glp jobs in Indiana are:

Infographic showing various Glp job openings in Indiana as of August 2026, with employment types broken down into 82% Full Time, 7% Part Time, 1% Temporary, 9% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $45,315 per year, or $21.8 per hour.

GLP Laboratory Systems Administrator

Corteva Agriscience

Indianapolis, IN โ€ข On-site

Other

Medical, Retirement, PTO

Posted yesterday

New


Job description

Corteva Agriscience is seeking a GLP Software Administrator to support R&D laboratory systems and applications in a regulated environment. This role will serve as a key partner to researchers, lab staff, IT, and business teams by maintaining system reliability, troubleshooting issues, supporting upgrades and implementations, and ensuring GLP compliance and data integrity. The ideal candidate will bring strong application support experience, knowledge of GLP/GxP requirements, and the ability to manage multiple priorities while supporting critical laboratory operations.

What Youโ€™ll Do:

  • Support, maintain, and improve R&D laboratory systems and applications to ensure availability, reliability, and performance for lab users.

  • Serve as a primary point of contact for researchers and laboratory staff, troubleshooting application, system, access, and usage issues.

  • Administer and maintain GLP-compliant software systems in accordance with applicable regulatory requirements.

  • Partner with researchers, lab staff, IT, and business leaders to gather requirements, resolve issues, and support system enhancements.

  • Support application configurations, upgrades, implementations, and system changes within laboratory environments while minimizing disruption to lab operations.

  • Ensure laboratory systems meet the needs of day-to-day R&D activities and remain stable, reliable, and fit for purpose.

  • Implement and maintain data integrity practices and protocols aligned with GLP standards.

  • Assist with software validation, qualification, testing, and documentation activities as required by GLP guidelines.

  • Prepare, maintain, and update documentation related to software administration, including SOPs, user guides, training materials, and support procedures.

  • Provide training and support to laboratory users on application functionality, best practices, and compliance-related processes.

  • Build and maintain strong working relationships with lab users, IT teams, and business stakeholders.

  • Stay current on industry trends, regulatory expectations, and advancements in GLP laboratory software solutions.

What Skills You Need:

  • Bachelorโ€™s degree in Life Sciences, Computer Science, Information Technology, or a related field.

  • Minimum of 5 years of experience in software administration, application support, or systems support, preferably in a laboratory, R&D, or technical environment.

  • Experience supporting IT applications or systems used in lab, R&D, scientific, or regulated environments.

  • Exposure to regulated environments such as GLP, GxP, or similar compliance frameworks.

  • Strong troubleshooting skills across applications, systems, user access, and user-reported issues.

  • Experience working directly with end users and cross-functional teams to resolve issues and support business needs.

  • Experience supporting application upgrades, system enhancements, configurations, or implementations.

  • Strong problem-solving skills with excellent attention to detail.

  • Strong communication and interpersonal skills, with the ability to explain technical concepts to non-technical users.

  • Ability to manage multiple priorities in a fast-paced environment.

  • Ability to work both independently and collaboratively as part of a team.

Preferred Qualifications

  • Experience with software validation and qualification processes in regulated environments.

  • Familiarity with laboratory software platforms such as SCIEX OS, Analyst, Chromeleon, MassHunter, Openlab CDS, Debra, and Laura.

  • Certification or formal training in GLP, GxP, software validation, or a related compliance area.

#LI-BB1

Benefits โ€“ How Weโ€™ll Support You:

  • Numerous development opportunities offered to build your skills

  • Be part of a company with a higher purpose and contribute to making the world a better place

  • Health benefits for you and your family on your first day of employment

  • Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays

  • Excellent parental leave which includes a minimum of 16 weeks for mother and father

  • Future planning with our competitive retirement savings plan and tuition reimbursement program

  • Learn more about our total rewards package here - Corteva Benefits (https://hrportal.ehr.com/LinkClick.aspx?fileticket=2Nre68t3vrs%3d&portalid=351)

  • Check out life at Corteva! www.linkedin.com/company/corteva/life

Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team.

Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.

Corteva Agriscienceโ„ข is an equal opportunity employer. We are committed to boldly embracing the power of inclusion, diversity, and equity to enrich the lives of our employees and strengthen the performance of our company, while advancing equity in agriculture. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. Discrimination, harassment and retaliation are inconsistent with our values and will not be tolerated. If you require a reasonable accommodation to search or apply for a position, please visit:Accessibility Page for Contact Information

For US Applicants: See the โ€˜Equal Employment Opportunity is the Lawโ€™ poster. To all recruitment agencies: Corteva does not accept unsolicited third party resumes and is not responsible for any fees related to unsolicited resumes.