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Scientific Affairs Associate Jobs in Georgia (NOW HIRING)

Becton, Dickinson and Company

The Regulatory Affairs Associate Director, Globalization is responsible for alignment and execution ... Bachelor's degree in science, engineering, or technology discipline required. * Minimum 10 years of ...

Daiichi Sankyo, Inc.

$153K - $230K/yr

... Associate Director MSL 5 or More Years' experience including medical & scientific affairs, clinical practice, research, academic or US managed markets preferred Previous experience in Oncology ...

Agilent

Clinical Affairs Scientist

Turin, GA · On-site +1

$105K - $197K/yr

... Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and ... Ensure scientific validity of reported results including statistical analysis, tabulation, and ...

WebMD

Content Associate (Oncology)

Atlanta, GA

$35K - $40K/yr

Role OverviewThe Content Associate is an integral entry-level member of the Medical Affairs Scientific Services team. This role provides critical process leverage for Medical Science Directors (MSDs ...

WebMD

Content Associate (Oncology)

Atlanta, GA · On-site

$35K - $40K/yr

Role Overview The Content Associate is an integral entry-level member of the Medical Affairs Scientific Services team. This role provides critical process leverage for Medical Science Directors (MSDs ...

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Scientific Affairs Associate information

What does a Scientific Affairs Associate do?

A Scientific Affairs Associate supports the development and communication of scientific information within organizations such as pharmaceutical, biotechnology, or medical device companies. Their responsibilities often include reviewing and summarizing scientific literature, preparing technical documentation, assisting with regulatory submissions, and serving as a liaison between research, regulatory, and commercial teams. They play a crucial role in ensuring scientific accuracy in company materials and helping translate complex data into understandable information for both internal and external stakeholders. This position typically requires a strong background in science, excellent communication skills, and attention to detail.

What are the key skills and qualifications needed to thrive as a Scientific Affairs Associate?

To thrive as a Scientific Affairs Associate, a strong background in life sciences, analytical thinking, and often an advanced degree (such as MS or PhD) are essential. Familiarity with regulatory databases, scientific literature search tools, and document management systems is typically required, along with experience in preparing scientific and regulatory documents. Excellent communication, attention to detail, and the ability to collaborate with cross-functional teams are standout soft skills for this role. These competencies are crucial for ensuring accurate scientific communication, regulatory compliance, and effective support of product development and approval processes.

How does a Scientific Affairs Associate typically collaborate with cross-functional teams in a healthcare or pharmaceutical company?

As a Scientific Affairs Associate, you will frequently work alongside clinical, regulatory, and marketing teams to ensure scientific accuracy and compliance in all communications and materials. Collaboration often involves reviewing clinical data, preparing scientific content for internal and external stakeholders, and supporting product launches or educational initiatives. This role requires clear communication and the ability to translate complex scientific information for diverse audiences, making teamwork and adaptability essential for success.

What are the most commonly searched types of Scientific Affairs jobs in Georgia?

The most popular types of Scientific Affairs jobs in Georgia are:

What are popular job titles related to Scientific Affairs Associate jobs in Georgia?

For Scientific Affairs Associate jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Scientific Affairs Associate jobs in Georgia look for?

The top searched job categories for Scientific Affairs Associate jobs in Georgia are:

What cities in Georgia are hiring for Scientific Affairs Associate jobs?

Cities in Georgia with the most Scientific Affairs Associate job openings:

Scientific Affairs Associate jobs near you
Infographic showing various Scientific Affairs Associate job openings in Georgia as of August 2026, with employment types broken down into 96% Full Time, and 4% Part Time. Highlights an 96% In-person, and 4% Remote job distribution.

Director of Regulatory & Scientific Affairs, Health & Wellness

Kennesaw, GA

Archer Daniels Midland
Manufacturing • 1 - 5K employees

7.9

Company rating: 7.9 out of 10

Based on 186 frontline employees who took The Breakroom Quiz

76th of 366 rated logistics

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Learn more about Archer Daniels Midlandexternal

Full-time

Re-posted 2 days ago

Job description

Director of Regulatory & Scientific Affairs, Health & Wellness - Based on-site at any ADM location in the US, including Kennesaw, GA, Decatur, IL, Erlanger, KY, Chicago, IL
Summary:
This role is responsible for providing local technical support for the definition and execution of the commercial strategy in North America. This role works in conjunction with the Global RSA H&W Head, and the cross-functional H&W team to leverage regulatory compliance of the H&W portfolio by leading the assessments of permissibility and suitability in North America (NA) and any registration or process associated, to unlock the market according to the business strategy.
Job purpose:
  • North America Regulatory and Scientific Affairs responsibility for ADM Health & Wellness (H&W) microbiome-based food supplements and other health-regulated ingredients.
  • Drive cross-functional collaboration, proactive regulatory risk management and mitigation while informing innovation and enabling market access and business growth.
  • Engaging and aligning with commercial partners to develop and implement regulatory strategies that enable ADM H&W business.
Responsibilities:
  • Own the gap analysis of Health & Wellness portfolio against regulatory requirements and other relevant guidelines, providing subsequent advice to relevant colleagues in order to develop the data to unlock the NA market according to the business strategy.
  • Lead and support the assessment and approval of the steps that require regulatory input and are related to innovation and/or permissibility and suitability of the H&W portfolio.
  • According to the metrics and KPIs established by H&W and RSA, own trending and root cause analysis of NA's KPIs and implements actions to ensure a positive trend according to H&W expectations and ADM policies and standards.
  • Lead regulatory feedback on topics related to claims and marketing materials intended for North America.
  • Own the Regulatory Risk Assessments related to the permissibility and suitability assessments of the H&W portfolio intended for North America, according to the current process and propose technical mitigation actions as applicable.
  • Own the preparation, review and submission of regulatory dossiers and applications for the H&W portfolio in North America and ensure accuracy, completeness and compliance with regulatory requirements in close collaboration with internal SMEs and external experts.
  • Works in conjunction with the global RSA team, as well as local ADM country colleagues to achieve new products authorizations, renewals and successful variations of H&W products manufactured in North America.
  • In conjunction with the Global RSA H&W Head, ensures regulatory compliance for ingredients and products throughout their lifecycle.
  • Leverage the regulatory service ADM provides to its customers in accordance with ADM policies and processes by representing RSA H&W in meetings with key customers and by leading the H&W RSA team responsible for North America.
  • Keep abreast of regulatory requirements, guidelines and industry best practices related to H&W ingredients and make strategic recommendations to senior management as risks and opportunities arise.
  • Ensure alignment and engagement of the NA H&W RSA teams, using common ways of working, for daily interactions of RSA and business/client stakeholders within the region.
  • In conjunction with relevant RSA colleagues, develops and manages regulatory positions by writing and reviewing regulatory documents (SOPs, Work Instructions, RSA statements and guidelines) according to the Document Management System.
  • Ensure North America RSA H&W team members are adequately resourced to serve the commercial and technical needs of business stakeholders regarding the H&W product portfolio and daily operations.
  • Ensure alignment and engagement of the NA H&W RSA teams, using common ways of working, for daily interactions of RSA and business/client stakeholders within the region.
Qualification and Experience:
  • Degree in Food technology or law, Chemistry, Biology or Biochemistry
  • 10+ years of experience in regulatory affairs within food supplements, health ingredients, and/or microbiome ingredients.
  • Proven experience managing complex regulatory submissions,
  • Knowledge of relevant regulations and standards for the food industry.
  • Strong understanding of US and Canada regulatory frameworks.
  • Experience in regulatory advocacy and industry representation desirable.
  • Strong organizational, attention to detail, communication, and strategic planning skills, with ability to operate cross-functionally and at various levels of the organization.
  • Hands-on experience with regulatory systems, RIMS, and documentation platforms is a plus.
Excited about this role but don't think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings.
ADM requires the successful completion of a background check. 
REF:111352BR

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