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Regulatory Associate Jobs in Indiana (NOW HIRING)

Warehouse Associate, 3rd shift

Fishers, IN

$15 - $17.75/hr

This role involves receiving, storing, picking, and packing GMP products while adhering to strict safety and regulatory standards. The warehouse associate will also support handling and delivery of ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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Showing results 1-20

Regulatory Associate information

See Indiana salary details

$16

$30

$46

How much do regulatory associate jobs pay per hour?

As of Jun 28, 2026, the average hourly pay for regulatory associate in Indiana is $30.65, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $36.35 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 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.

What is a Regulatory Associate?

A Regulatory Associate is a professional who supports regulatory affairs teams in ensuring that a company complies with all relevant laws and regulations, particularly in industries like pharmaceuticals, biotechnology, and medical devices. They assist in preparing, submitting, and maintaining regulatory filings and documentation required by government agencies. Regulatory Associates also help track changes in regulations and support product development by ensuring all necessary approvals are obtained for products to enter the market.

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 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 the most commonly searched types of Regulatory jobs in Indiana? The most popular types of Regulatory jobs in Indiana are:
What are popular job titles related to Regulatory Associate jobs in Indiana? For Regulatory Associate jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Regulatory Associate jobs? Cities in Indiana with the most Regulatory Associate job openings:
Warehouse Associate, 3rd shift

Warehouse Associate, 3rd shift

INCOG BioPharma Services

Fishers, IN

$14.50 - $17/hr

Full-time

Posted 23 days ago


Job description

Warehouse Associate (3rd Shift ) Summary

INCOG Biopharma Services is looking for a Warehouse Associate to join our growing team.  This role is key to the material receipt, storage, handling, movement and reconciliation of inventory at the INCOG facility. This individual will help with the development and continuous improvement of processes and procedures.


The Warehouse Associate is responsible for ensuring the accurate and efficient handling, storage, and distribution of GMP products within the warehouse. This role involves receiving, storing, picking, and packing GMP products while adhering to strict safety and regulatory standards.  The warehouse associate will also support handling and delivery of NON-GMP materials throughout the facility. Must be able to meet the physical requirements of this job including operating a forklift, lifting 50lbs or more and being on your feet for 4-6 hours daily.


Essential Job Functions:

  • Receive incoming pharmaceutical shipments and verify contents against purchase orders, materials specifications and receiving in line with INCOG SOP’s.

  • Receive incoming non-pharmaceutical shipments and verify contents against the purchase order. Delivering to internal customers.

  • Inspect products for damage, discrepancies, or expired items and report any issues to the Warehouse Manager.

  • Store pharmaceutical products in designated areas according to material specifications and regulatory requirements.

  • Maintain accurate inventory records using warehouse management systems (WMS/SAPbyDesign).

  • Conduct regular cycle counts and assist in periodic physical inventory audits.

  • Pick and pack orders accurately and efficiently to meet internal customer demands

  • Ensure all orders are labeled correctly and prepared for internal delivery according to company standards.

  • Able to use barcode scanners and other technology to track and manage inventory.

  • Adhere to all safety, quality, and regulatory guidelines, including Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).

  • Maintain a clean and organized work environment to prevent contamination and ensure product integrity.

  • Assist in maintaining records for regulatory inspections and audits.

  • Operate warehouse equipment such as forklifts, pallet jacks, and conveyor systems safely and efficiently.

  • Perform routine maintenance checks on equipment and report any malfunctions to the Warehouse Manager.

  • Work collaboratively with other warehouse associates and departments to achieve operational goals.

  • Participate in team meetings and training sessions to stay updated on company policies and procedures.


Job Requirements:

  • 2-4  years previous experience in a warehouse or logistics environment, preferably in the pharmaceutical industry.

  • Strong attention to detail and accuracy.

  • Excellent organizational and time management skills.

  • Ability to operate warehouse equipment safely.

  • Proficiency with warehouse management systems (WMS) and barcode scanning technology.


    Physical Requirements:

  • Ability to lift and move objects up to [insert weight] pounds.

  • Certification in handling hazardous materials (preferred but not required).

  • Fast-paced warehouse environment with exposure to pharmaceutical products.


Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.


If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.


INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind.  All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.


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