1

Scientific Affairs Associate Jobs in Florida (NOW HIRING)

Position Summary The Regulatory Affairs Associate supports the organization's product stewardship ... Bachelor's degree in Chemistry, Environmental Science, Toxicology, Biology, Chemical Engineering ...

Ensure scientific work, data generation, and project activities comply with applicable requirements and standards; recommend and apply appropriate scientific approaches for product updates and future ...

Ensure scientific work, data generation, and project activities comply with applicable requirements and standards; recommend and apply appropriate scientific approaches for product updates and future ...

Bachelor's degree in a related field such as biology, chemistry, or pharmaceutical sciences. * Previous experience in a regulatory affairs role within the pharmaceutical industry is preferred.

... contact with Associate Director of Regulatory Affairs. * Responsible for preparation, review ... Bachelors degree in Pharmaceutical, Biological or Chemical Science or related field. Advanced ...

An Associate's degree from a regionally accredited institution. • Experience: At least 3 years of ... Preferred Qualifications: • A Bachelor's degree from an accredited college in Political Science ...

An Associate's degree from a regionally accredited institution. Experience: At least 3 years of ... A Bachelor's degree from an accredited college in Political Science, Public Administration ...

... Associate Dean of Academic Affairs in managing advising and academic support for graduate programs in the College of Health Professions and Sciences. The manager assists graduate students with ...

next page

Showing results 1-20

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 Florida?

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

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

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

Infographic showing various Scientific Affairs Associate job openings in Florida as of August 2026, with employment types broken down into 80% Full Time, 15% Part Time, and 5% Nights. Highlights an 85% In-person, 5% Hybrid, and 10% Remote job distribution.

Regulatory Affairs Associate

ITW Car Care

Lakeland, FL • Hybrid

Full-time

Posted 10 days ago


Job description

Job Description:

About Us:

ITW Car Care is a division of Illinois Tool Works (ITW), specializing in automotive aftermarket products. The division offers a diverse portfolio of brands such as Rain-X wiper blades, visibility enhancing products, and water repellent treatments, including our 2-in-1 Glass Cleaner. Black Magic to support all your wheel and tire needs including Tire Wet.

Position Summary

The Regulatory Affairs Associate supports the organization's product stewardship and regulatory compliance programs by ensuring products meet applicable environmental, health, safety, transportation, and chemical regulatory requirements. This role works closely with Regulatory Affairs, EHS & Quality, R&D, Product Development, Supply Chain, Marketing, and Operations to assess product compliance, maintain regulatory documentation, and support product lifecycle management activities. This role will be located in Lakeland, FL.

Key ResponsibilitiesRegulatory Compliance
  • Monitor global, federal, state, and local regulations impacting products and raw materials.
  • Support compliance evaluations for regulations such as TSCA, CEPA, GHS, Prop 65, PFAS restrictions, VOC regulations, and other applicable chemical management requirements.
  • Maintain regulatory databases and compliance records.
  • Assist in preparing regulatory submissions, notifications, and registrations as required.

Product Stewardship

  • Conduct product compliance reviews throughout the product lifecycle.
  • Evaluate raw material and finished product compositions for regulatory compliance.
  • Support hazard assessments and risk evaluations for new and existing products.
  • Ensure products are classified, labeled, and documented in accordance with applicable regulations.

Documentation & Data Management

  • Create, review, and maintain Safety Data Sheets (SDSs), product labels, and technical documentation.
  • Manage supplier compliance documentation, including SDSs, certificates, and regulatory declarations.
  • Maintain accurate compliance data within company systems and databases.
  • Support customer requests related to product regulatory and stewardship information.

Cross-Functional Collaboration

  • Partner with Research & Development teams during product development initiatives.
  • Collaborate with Supply Chain and Procurement to evaluate supplier regulatory information.
  • Support Marketing and Sales by providing regulatory guidance on product claims and market access requirements.
  • Assist Manufacturing and Quality teams with product compliance-related investigations and corrective actions.

Compliance Support

  • Participate in internal and external compliance audits.
  • Assist with responses to customer compliance questionnaires and regulatory inquiries.
  • Support continuous improvement initiatives within the Product Stewardship function.
QualificationsEducation
  • Bachelor's degree in Chemistry, Environmental Science, Toxicology, Biology, Chemical Engineering, Regulatory Affairs, or a related scientific discipline required.

Experience

  • 1-3 years of experience in Product Stewardship, Regulatory Affairs, Environmental Health & Safety (EHS), Product Compliance, Quality, or a related field preferred.
  • Internship or co-op experience in regulatory compliance or chemical management may be considered.

Knowledge & Skills

  • Basic understanding of global chemical regulations and product compliance requirements.
  • Familiarity with GHS hazard communication and Safety Data Sheet authoring.
  • Knowledge of chemical inventory management and product composition review processes.
  • Strong analytical and problem-solving skills.
  • Excellent organizational skills and attention to detail.
  • Effective written and verbal communication skills.
  • Proficiency with Microsoft Office applications and regulatory data management systems.

Preferred Qualifications

  • Experience with SDS authoring software.
  • Knowledge of automotive aftermarket, consumer products, chemical manufacturing, or industrial product regulations.
  • Familiarity with ERP systems, or regulatory compliance databases.
  • Professional certifications related to product stewardship or regulatory affairs are a plus.

Competencies

  • Attention to Detail
  • Regulatory Compliance Mindset
  • Analytical Thinking
  • Collaboration and Teamwork
  • Customer Focus
  • Project Management
  • Continuous Learning
  • Effective Communication

Working Conditions

  • Primarily office or hybrid work environment.
  • Ability to manage multiple tasks and deadlines in a fast-paced environment.

Reporting Structure

Reports To: Sr. Quality and Regulatory Manager

ITW is an equal opportunity employer. We value our colleagues’ unique perspectives, experiences and ideas and create workplaces where everyone can develop their careers and perform to their full potential. 


As an equal employment opportunity employer, ITW is committed to equal employment opportunity and fair treatment for employees, beginning with the hiring process and continuing through all aspects of the employment relationship. 


All qualified applicants will receive consideration for employment without regard to race, color, sex, gender identity, sexual orientation, religion, national origin, age, disability, protected Veteran status or any other characteristic protected by applicable federal, state, or local laws.