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Fda Consulting Jobs in Indiana (NOW HIRING)

Amaris Consulting

Packaging Engineer

Warsaw, IN · On-site

Knowledge of ISO 11607, ISO 13485, and/or FDA requirements. * Exposure to packaging validation ... Consulting promotes equal opportunities. We are committed to bringing together people from diverse ...

Eightelevengroup

Software Quality Engineer

Warsaw, IN · On-site

$76 - $88/hr

Provide technical support for audits of software suppliers and consultants, including cybersecurity ... Provide expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance ...

Eliquent Life Sciences, Inc

CQV Engineer

Indianapolis, IN · On-site

$80K - $95K/yr

ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science ... Working knowledge of FDA and cGMP regulations and documentation practice * Ability to read and ...

Brooksource

Software Quality Engineer

Indianapolis, IN · On-site

$55 - $64/hr

Provide technical support for audits of software suppliers and consultants, including cybersecurity ... Provide expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance ...

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$49

$76

How much do fda consulting jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for fda consulting in Indiana is $49.97, according to ZipRecruiter salary data. Most workers in this role earn between $20.82 and $66.35 per hour, depending on experience, location, and employer.

What is an FDA consulting?

An FDA Consulting job involves providing expert guidance to businesses seeking regulatory approval for their products from the U.S. Food and Drug Administration (FDA). Consultants help companies navigate complex FDA regulations, ensure compliance, and prepare necessary documentation for submissions. They may work with pharmaceuticals, medical devices, food, and biotech industries. Their role includes strategy development, risk assessment, and communication with the FDA to facilitate approvals and avoid compliance issues.

What does an FDA consultant do?

As an FDA Consultant, your day might involve reviewing regulatory documentation, preparing submissions for FDA approval, and advising clients on compliance strategies. You’ll often attend meetings with cross-functional teams including R&D, quality assurance, and legal experts to ensure alignment on regulatory requirements. Consultants also stay updated on changes in FDA guidelines, draft correspondence to regulatory agencies, and address client questions or concerns. This dynamic role requires adaptability and strong collaboration skills to manage multiple projects and effectively support clients through all stages of the regulatory process.

What skills and qualifications are needed for FDA consulting?

To thrive in FDA Consulting, you need expertise in regulatory affairs, a deep understanding of FDA guidelines, and often a degree in life sciences or a related field. Familiarity with regulatory submission systems such as eCTD, knowledge of GxP standards, and certifications like RAC (Regulatory Affairs Certification) are valuable. Strong communication, analytical thinking, and project management skills set outstanding consultants apart. These competencies are essential to effectively guide clients through complex regulatory landscapes and ensure successful product approvals.

What are the most commonly searched types of Fda Consulting jobs in Indiana?

The most popular types of Fda Consulting jobs in Indiana are:

What are popular job titles related to Fda Consulting jobs in Indiana?

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

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

The top searched job categories for Fda Consulting jobs in Indiana are:

Fda Consulting jobs near you
Infographic showing various Fda Consulting job openings in Indiana as of August 2026, with employment types broken down into 70% Full Time, 16% Part Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $103,936 per year, or $50 per hour.

EPA Regulatory Consultant

Scientific & Regulatory Consultants, Inc.

Columbia City, IN • On-site

Other

Re-posted 13 days ago

Job description

Company Description

Scientific & Regulatory Consultants, Inc. (SRC) provides comprehensive regulatory services to the antimicrobial and pesticide industry, supporting products regulated by EPA, FDA, and international authorities. The team brings more than 220 years of combined experience and maintains active memberships in leading industry organizations, reflecting deep engagement with evolving regulatory standards. SRC specializes in translating complex scientific and regulatory requirements into practical strategies for testing, registration, and marketing. The company offers robust state registration and compliance services, supported by established relationships with agencies and a web-based SERVICE Portal for accessing registration data. Clients range from entrepreneurial startups to multinational corporations worldwide, and SRC is recognized for its commitment, integrity, and collaborative approach. Join one of the premier regulatory consulting teams in the U.S. You’ll navigate EPA FIFRA, California DPR, and international frameworks, build lasting client relationships, and help bring pesticide and antimicrobial products to market.


Role Description

The EPA Regulatory Consultant role is a full-time, remote position responsible for guiding clients through U.S. EPA regulatory processes for antimicrobial and pesticide products.


In this role you will:

•  Build and maintain relationships with clients, labs, and government regulators

•  Prepare EPA OPP/FIFRA, California DPR, Health Canada, and other regulatory submissions

•  Develop client-specific regulatory strategies and solutions

•  Negotiate with government agencies on behalf of SRC and clients

•  Review technical reports, labels, SDSs, and adverse event reports for compliance

•  Track regulatory trends; communicate challenges and opportunities to management

•  Support your clients’ business development, audits, training, and trade association activities


You will collaborate with internal team members and client stakeholders to plan testing programs, align product claims with regulatory standards, and address agency questions or data requests. The role also involves maintaining up-to-date knowledge of relevant statutes, regulations, and guidance documents, monitoring regulatory changes, and advising clients on compliance implications. Additional responsibilities include managing project timelines and deliverables, supporting state registration and compliance efforts, and contributing to internal best practices and knowledge-sharing.


Qualifications

•  College degree or equivalent regulatory work experience

•  Bachelor's degree preferred

•  Strong written, verbal, and digital communication skills

•  Ability to handle sensitive situations with tact and discretion

•  Proficiency in Office 365 (Word, Excel, PowerPoint, Outlook)

•  Experience with:

•  EPA FIFRA and California DPR regulations and     policies for pesticides

•  EPA and FDA Good Laboratory Practices

•  Good Manufacturing Practices

•  Canada and EU regulations

  • Fertilizers and plant/soil amendment

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