Bilingual Regulatory Affairs Associate (English and Spanish)

5TH HQ

Fort Lauderdale, FL

JOB DETAILS
SALARY
$20–$24 Per Hour
SKILLS
Academic Background, Analysis Skills, Change Control, Computer Skills, Control Systems, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Customer Support/Service, Detail Oriented, Document Control, Document Management, Documentation, English Language, GMP (Good Manufacturing Practices), Laboratory Notebook, Maintain Compliance, Manufacturing, Multilingual, Organizational Skills, Production Control, Quality Assurance Methodology, Quality Control, Regulations, Regulatory Compliance, Regulatory Submissions, Spanish Language, Standard Operating Procedures (SOP), Training/Teaching, Vendor/Supplier Evaluation
LOCATION
Fort Lauderdale, FL
POSTED
18 days ago

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.

 

 

About the Company

5

5TH HQ