ZipRecruiter

Log In

1

Scientific Affairs Associate Jobs (NOW HIRING)

3M

Sr. Regulatory Affairs Associate

Maplewood, MN · On-site

$124K - $151K/yr

Sr. Regulatory Affairs Associate Collaborate with Innovative 3Mers Around the World Choosing where ... Bachelor's degree in Chemistry, Material Science, Technical or related degree from an accredited ...

3M

Sr. Regulatory Affairs Associate

Maplewood, MN

$124K - $151K/yr

Sr. Regulatory Affairs Associate Collaborate with Innovative 3Mers Around the World Choosing where ... Bachelor's degree in Chemistry, Material Science, Technical or related degree from an accredited ...

3M

Sr. Regulatory Affairs Associate

Austin, TX

$124K - $151K/yr

Sr. Regulatory Affairs Associate Collaborate with Innovative 3Mers Around the World Choosing where ... Bachelor's degree in Chemistry, Material Science, Technical or related degree from an accredited ...

Oscar Health

Associate, Government Affairs

Washington, DC · Remote

$87K - $114K/yr

We're hiring an Associate, Government Affairs to join our Government Affairs. Oscar is the first ... Requirements: * Bachelor's degree in legal studies, political science, public policy, public ...

Oscar Health

Associate, Government Affairs

New York, NY · Hybrid

$96K - $127K/yr

We're hiring an Associate, Government Affairs to join our Government Affairs. Oscar is the first ... Requirements: * Bachelor's degree in legal studies, political science, public policy, public ...

next page

Showing results 1-20

All JobsScientific Affairs Associate Jobs

Scientific Affairs Associate information

See salary details

$13

$31

$52

How much do scientific affairs associate jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for scientific affairs associate in the United States is $31.48, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $40.14 per hour, depending on experience, location, and employer.

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 key skills and qualifications needed to thrive as a Scientific Affairs Associate, and why are they important?

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.

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.
More about Scientific Affairs Associate jobs
What cities are hiring for Scientific Affairs Associate jobs? Cities with the most Scientific Affairs Associate job openings:
What are the most commonly searched types of Scientific Affairs jobs? The most popular types of Scientific Affairs jobs are:
What states have the most Scientific Affairs Associate jobs? States with the most job openings for Scientific Affairs Associate jobs include:
What job categories do people searching Scientific Affairs Associate jobs look for? The top searched job categories for Scientific Affairs Associate jobs are:
Scientific Affairs Associate jobs near you
Infographic showing various Scientific Affairs Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $65,473 per year, or $31.5 per hour.
Bilingual Regulatory Affairs Associate (English and Spanish)

Bilingual Regulatory Affairs Associate (English and Spanish)

5TH HQ

Fort Lauderdale, FL • On-site

$20 - $24/hr

Full-time

Posted 23 days ago

Job description

We are currently seeking a Bilingual Regulatory Affairs Associate (English/Spanish) for a manufacturing company in Davie, FL. This opportunity is ideal for candidates with a Science-related educational background, including recent graduates or individuals currently finishing their degree.

We are open to considering candidates whose academic background, technical knowledge, and potential can complement or substitute previous professional experience.

Davie, FL

Schedule: Monday – Friday
8:30 AM – 5:00 PM

Salary Range: $20 – $24/hr

Responsibilities:

  • Develop, review, edit, and maintain controlled documentation such as:
    • Standard Operating Procedures (SOPs)
    • Forms and specifications
    • Testing methods
    • Validation reports
    • Complaints and CAPA reports
    • Protocols and deviations
    • Laboratory notebooks
    • Product monographs
    • Certificates of Analysis templates
  • Review and maintain Master Formulas.
  • Coordinate document control systems and SOP distribution.
  • Support Change Control processes and compliance activities.
  • Prepare annual GMP training materials and coordinate training sessions.
  • Coordinate vendor qualification audits and supplier documentation.
  • Assist with customer and regulatory audits.
  • Prepare regulatory documentation submissions as required.
  • Maintain documentation databases, records, and archival systems.
  • Ensure compliance with cGMP regulations and company procedures.
  • Perform additional duties assigned by management.

Qualifications:

  • Bachelor's Degree in Science or related field preferred.
  • Recent graduates or candidates currently completing their degree are encouraged to apply.
  • Bilingual English/Spanish required.
  • 1–3 years of experience preferred, but not required.
  • Knowledge of GMP regulations preferred.
  • Computer literate.
  • Detail-oriented with strong organizational skills.
  • Previous experience in Production, Quality Control, or Regulatory Affairs is a plus.

Benefits:

  • Full-time opportunity.
  • Professional growth potential.
  • Stable work environment.
5th HQ logo

About 5th HQ

Sourced by ZipRecruiter

We are a boutique Staffing & Recruiting agency that provides a full range of employment solutions that include full-time, temporary, and part-time employment in a wide range of positions, including Professional, Light Industrial, and Office Services.

Industry

Recruiting and staffing services

Headquarters location

Plantation, FL, US

View All 5th HQ Jobs