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Regulatory Affairs Associate Two Jobs in Boca Raton, FL

We are currently seeking a detail-oriented and motivated Regulatory Affairs Specialist. This role is crucial in ensuring that our products comply with all regulatory requirements. If you are ...

Associates are part of a stimulating and exciting environment in which they can develop their ... Management experience (at least 2 years of project or supervisory management) It is Terumo's policy ...

Provides accurate and timely regulatory guidance to all company functions while maintaining frequent contact with Associate Director of Regulatory Affairs. * Responsible for preparation, review ...

... to associates and affiliates. Review and provide regulatory authorization for Nonconformance ... Minimum 5 years direct experience in regulatory affairs (preferably in the medical device/drug or ...

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Regulatory Affairs Associate Two information

See Boca Raton, FL salary details

$18

$37

$59

How much do regulatory affairs associate two jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for regulatory affairs associate two in Boca Raton, FL is $37.55, according to ZipRecruiter salary data. Most workers in this role earn between $30.10 and $44.47 per hour, depending on experience, location, and employer.

What is the difference between Regulatory Affairs Associate Two vs Regulatory Affairs Associate One?

AspectRegulatory Affairs Associate TwoRegulatory Affairs Associate One
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, entry-level certifications may suffice
Work EnvironmentMid-level regulatory team, more independent responsibilitiesEntry-level, supervised tasks within regulatory teams
Employer & Industry UsagePharmaceutical, biotech, medical device companiesSimilar industries, often within larger regulatory departments
Common Search & Comparison IntentUnderstanding role progression and responsibilitiesEntry-level position details and requirements

The main difference between Regulatory Affairs Associate Two and Regulatory Affairs Associate One lies in experience and responsibilities. Associate Two typically has more experience, handles more complex tasks independently, and may require relevant certifications. Associate One is an entry-level role focused on foundational regulatory tasks. Both roles are common in the pharmaceutical and biotech industries, with Associate Two representing a more advanced position within the regulatory team.

Is regulatory affairs a stable career?

Regulatory affairs is generally considered a stable career due to consistent demand in industries like pharmaceuticals, medical devices, and biotechnology. Professionals in this field often require specialized knowledge of regulations and may hold certifications, which support long-term employment opportunities.

What job categories do people searching Regulatory Affairs Associate Two jobs in Boca Raton, FL look for?

The top searched job categories for Regulatory Affairs Associate Two jobs in Boca Raton, FL are:

What cities near Boca Raton, FL are hiring for Regulatory Affairs Associate Two jobs?

Cities near Boca Raton, FL with the most Regulatory Affairs Associate Two job openings:

Bilingual Regulatory Affairs Associate (English and Spanish)

5TH HQ

Fort Lauderdale, FL • On-site

$20 - $24/hr

Full-time

Re-posted 25 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