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Regulatory Associate Jobs in Lebanon, IN (NOW HIRING)

Ascension

Regulatory Research Specialist

Carmel, IN · On-site

We empower our 97,000+ associates to bring their skills and expertise every day to reimagining healthcare, together. Recognized as one of the Best 150+ Places to Work in Healthcare and a Military ...

SUPPLY.com

Warehouse Associate

Indianapolis, IN · On-site

$15.25 - $18.25/hr

Must adhere to all safety regulations, including the correct usage of personal protective equipment ... our associates. Our competitive offering not only includes benefits like health, dental, vision ...

Ferguson Enterprises, LLC

Warehouse Associate

Indianapolis, IN · On-site

$15.25 - $18.25/hr

Must adhere to all safety regulations, including the correct usage of personal protective equipment ... our associates. Our competitive offering not only includes benefits like health, dental, vision ...

Lighting Unlimited

Warehouse Associate

Indianapolis, IN · On-site

$15.25 - $18.25/hr

Must adhere to all safety regulations, including the correct usage of personal protective equipment ... our associates. Our competitive offering not only includes benefits like health, dental, vision ...

Ferguson Enterprises Inc.

Warehouse Associate

Indianapolis, IN · On-site

$15.25 - $18.25/hr

Must adhere to all safety regulations, including the correct usage of personal protective equipment ... our associates. Our competitive offering not only includes benefits like health, dental, vision ...

HP Products

Warehouse Associate

Indianapolis, IN · On-site

$15.25 - $18.25/hr

Must adhere to all safety regulations, including the correct usage of personal protective equipment ... our associates. Our competitive offering not only includes benefits like health, dental, vision ...

eTeam

Warehouse Associate

Westfield, IN · On-site

$15.25 - $18.25/hr

Warehouse Associate Under general supervision, the Warehouse Associate is responsible for material ... Comply with FDA regulations, applicable regulatory requirements, company policies, operating ...

Axelon

Warehouse Associate

Westfield, IN · On-site

$15.25 - $18.25/hr

Warehouse Associate Location: Westfield, IN Hours: 6:00 AM - 2:30 PM Working under general ... Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ...

Hire Talent

Warehouse Associate

Westfield, IN · On-site

$15.25 - $18.25/hr

Warehouse Associate Location: Westfield, IN 46074 Duration: 12 months of contract with possible ... Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies ...

Rural King

Firearms Associate

Avon, IN · On-site

Associate Assistance Program * RK Cares Associate Hardship Program * 24/7 Chaplaincy Services ... Your in-depth knowledge of firearms regulations, safety practices, and product features will ...

Rural King

Firearms Associate

Avon, IN

RK Cares Associate Hardship Program * 24/7 Chaplaincy Services What You'll do The purpose of a ... Your in-depth knowledge of firearms regulations, safety practices, and product features will ...

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All JobsRegulatory Associate JobsRegulatory Associate Jobs in Lebanon, IN

Regulatory Associate information

See Lebanon, IN salary details

$16

$30

$46

How much do regulatory associate jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for regulatory associate in Lebanon, IN is $30.85, according to ZipRecruiter salary data. Most workers in this role earn between $23.51 and $36.63 per hour, depending on experience, location, and employer.

What does a regulatory associate do?

As a regulatory associate or regulatory affairs associate, your job is to coordinate compliance with internal—and occasionally external—regulations. This work involves checking each inspection review for accuracy, using safety data sheets (SDS), gathering and compiling documentation for products, and submitting material for license renewals and registrations. In this role, you often create management templates, study existing report documents, oversee the collection of consent forms, and audit the company for any sign of regulatory noncompliance. Some regulatory associates frequently travel to perform audits at various locations. Depending on the industry, you may have additional tasks that involve meeting state or federal guidelines.

What are the key skills and qualifications needed to thrive as a regulatory associate, and why are they important?

To thrive as a Regulatory Associate, you need strong attention to detail, knowledge of regulatory guidelines (such as FDA or EMA), and a relevant degree in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and electronic common technical document (eCTD) software is typically required. Excellent organizational skills, communication abilities, and the capacity to manage deadlines make candidates stand out. These skills ensure accurate regulatory submissions, compliance with evolving regulations, and effective collaboration across teams, all of which are crucial for product approvals and market access.

What are some common challenges regulatory associates face when working with cross-functional teams?

Regulatory Associates often work closely with teams from R&D, quality assurance, clinical, and legal departments to ensure compliance throughout product development and approval processes. A common challenge is navigating differing priorities and timelines among these groups, which requires strong communication and organizational skills. Additionally, Regulatory Associates must interpret and clarify complex regulatory requirements to various stakeholders, ensuring everyone is aligned and informed. Building collaborative relationships and proactively addressing potential misunderstandings are key to overcoming these challenges.

What is the difference between Regulatory Associate vs Compliance Specialist?

AspectRegulatory AssociateCompliance Specialist
Required CredentialsBachelor's degree in life sciences, regulatory affairs, or related field; certifications like RAC are a plusBachelor's degree in law, business, or related; certifications like CCEP may be relevant
Work EnvironmentPharmaceutical, biotech, or medical device companies; regulatory departmentsCorporate compliance departments across various industries, including healthcare and finance
Employer & Industry UsageUsed in regulated industries to prepare and submit regulatory documentsUsed to ensure company adherence to laws and regulations, often involving audits and policy development

The Regulatory Associate primarily focuses on preparing and managing regulatory submissions within life sciences industries, while the Compliance Specialist ensures ongoing adherence to laws and regulations across various sectors. Both roles require similar educational backgrounds and certifications, but their core responsibilities and work environments differ slightly, with Regulatory Associates working more directly with regulatory agencies and Compliance Specialists focusing on internal compliance processes.

Is regulatory associate high paying?

Regulatory associates typically earn a competitive salary that varies by industry, location, and experience level. In general, the role offers moderate to high pay, especially for those with specialized knowledge of regulations, certifications, or experience in highly regulated sectors like pharmaceuticals or healthcare.
More about Regulatory Associate jobs

What cities near Lebanon, IN are hiring for Regulatory Associate jobs?

Cities near Lebanon, IN with the most Regulatory Associate job openings:

Regulatory Associate jobs near you
Infographic showing various Regulatory Associate job openings in Lebanon, IN as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 26% Part Time, 1% Temporary, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $64,174 per year, or $30.9 per hour.

Associate Director, Regulatory Affairs - Biologics

Indianapolis, IN • On-site

Elanco Animal Health Incorporated
Pharmaceutical and Medicine Manufacturing • 5 - 10K employees

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

49th of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by parents

Learn more about Elanco Animal Health Incorporatedexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 days ago

Job description

At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Your Role
As Associate Director, Regulatory Affairs - Biologics, you will lead regulatory strategy for biologics and vaccine programs supporting Animal Health innovation. This role guides regulatory activities across development and lifecycle management, partnering closely with R&D, Manufacturing, Quality, Technical Operations, and global regulatory stakeholders.
The ideal candidate brings experience in biologics, vaccines, biotechnology, or pharmaceutical regulatory affairs and has supported regulatory strategy, health authority interactions, and regulatory submissions. Experience in Animal Health is valued but not required.
This is an opportunity to apply your biologics regulatory expertise to innovative development programs while helping advance products that improve animal health globally.
Your Responsibilities
  • Lead regulatory strategy for biologics and vaccine programs across development and lifecycle management activities
  • Serve as a primary regulatory contact for interactions with health authorities, including FDA, USDA/CVB, EMA, and other global agencies
  • Drive planning, preparation, and submission of regulatory dossiers, agency responses, and supporting documentation
  • Provide regulatory guidance on biologics development, manufacturing changes, tech transfer, and lifecycle management
  • Partner with R&D, Manufacturing, Quality, Technical Operations, and other stakeholders to align regulatory strategy with program goals

What You Need to Succeed (minimum qualifications)
  • Education: Bachelor's degree in a scientific or technical discipline required
  • Experienced product Regulatory Affairs professional with 5+ years of direct RA experience, ideally biologics/vaccines or CMC, who has owned regulatory strategy, submissions and agency interactions and is either Indianapolis-based or clearly willing to relocate.
  • Experience supporting regulatory strategy, regulatory submissions, health authority interactions, or agency responses
  • Knowledge of biologics development, manufacturing processes, and product lifecycle management
  • Ability to work cross-functionally and influence decisions in a matrixed environment

What Will Give You a Competitive Edge (preferred qualifications)
  • Experience in Animal Health, Veterinary Biologics, Veterinary Vaccines, or related regulatory environments
  • Experience in Biologics CMC Regulatory Affairs
  • Familiarity with USDA-CVB, FDA-CVM, EMA, and VICH regulatory requirements
  • Experience supporting manufacturing changes, tech transfer, or post-approval regulatory activities
  • Experience supporting global or multi-regional regulatory programs

Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
• Multiple relocation packages
• Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
• 8-week parental leave
• 9 Employee Resource Groups
• Annual bonus offering
• Flexible work arrangements
• Up to 6% 401K matching
Full-time equivalent employees also will be eligible for a company bonus (depending partly on company and individual performance). Additionally, Elanco offers a comprehensive benefit program to eligible employees that includes a company-matching 401(k); vacation benefits; eligibility for medical, dental, vision, and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).
Elanco reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion, and Elanco's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Elanco employees.
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#LI-RH1
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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