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Regulatory Affairs Specialists in Puerto Rico

Regulatory Affairs Specialists in Puerto Rico

Considering working as a Regulatory Affairs Specialists in Puerto Rico? Here’s what you need to know. Examine, evaluate, and investigate eligibility for or conformity with laws and regulations governing contract compliance of licenses and permits, and perform other compliance and enforcement inspection and analysis activities not classified elsewhere. Excludes “Financial Examiners" (13-2061), “Tax Examiners and Collectors, and Revenue Agents” (13-2081), “Occupational Health and Safety Specialists” (19-5011), “Occupational Health and Safety Technicians” (19-5012), “Transportation Security Screeners” (33-9093), “Agricultural Inspectors” (45-2011), “Construction and Building Inspectors” (47-4011), and “Transportation Inspectors” (53-6051).

What do Regulatory Affairs Specialists Make in Puerto Rico?

For regulatory affairs specialists working in Puerto Rico, wages run about $46,570 per year (or roughly $22.39/hour).Annual wages span from $29,790 at the 10th percentile to $98,550 at the 90th percentile.

Wage Statistic Annual Hourly
10th percentile $29,790 $14.32
25th percentile $36,040 $17.33
Median (50th) $46,570 $22.39
75th percentile $64,550 $31.03
90th percentile $98,550 $47.38
Salary ranges for Regulatory Affairs Specialists in Puerto Rico

Location quotient — how concentrated this career is in Puerto Rico compared to the national average — is 2.00, indicating that regulatory affairs specialists are more concentrated here than the national average.

National Wage Comparison

Nationally, regulatory affairs specialists earn a median of $85,399 per year ($41.06/hour), lower than the Puerto Rico median.

Regulatory Affairs Specialists earnings in Puerto Rico vs. the national average

Employment Outlook

Nationally, total employment in this occupation is 326,183 regulatory affairs specialists in the U.S.. In Puerto Rico alone, about 4,840 people work in this role. That’s higher than the typical state, which employs around 4,100 regulatory affairs specialists.

Regulatory Affairs Specialists in Puerto Rico vs. the average state Forecasted number of jobs for Regulatory Affairs Specialists

Top Puerto Rico Metros for Regulatory Affairs Specialists

The largest metro-area employers of regulatory affairs specialists in Puerto Rico.

Metro Area Number Employed Annual Median Salary
San Juan-Bayamon-Caguas, PR 4,070 $47,760
Aguadilla, PR 310 $36,040
Ponce, PR 170 $43,630
Mayaguez, PR 130 $44,870
Arecibo, PR 40 $46,000

Top States for Regulatory Affairs Specialists Employment

These states have the highest employment of regulatory affairs specialists work.

State Number Employed
California 47,420
Texas 39,870
Florida 31,610
New York 23,690
Pennsylvania 15,320
Virginia 15,120
Georgia 13,730
New Jersey 12,000
Arizona 11,590
Massachusetts 11,460
Ohio 11,320
Washington 10,820
Illinois 10,190
Michigan 9,660
North Carolina 9,080
Maryland 8,860
Tennessee 8,140
Colorado 7,470
Missouri 7,000
Minnesota 6,460

Highest-Paying States for Regulatory Affairs Specialists

These states pay the most for regulatory affairs specialists.

State Annual Median Salary
District of Columbia $103,010
New Jersey $93,520
Massachusetts $92,890
California $92,350
Alaska $88,730
Vermont $88,550
Delaware $88,450
Maryland $87,580
Connecticut $87,210
Maine $86,940

Skills

Top regulatory affairs specialists skills, rated on an importance scale of 0 to 5:

Writing  4.0 / 5
0
5
Active Listening  4.0 / 5
0
5
Speaking  4.0 / 5
0
5
Critical Thinking  3.9 / 5
0
5
Reading Comprehension  3.9 / 5
0
5
Judgment and Decision Making  3.9 / 5
0
5

Knowledge Areas

Important knowledge areas for this occupation, rated on an importance scale of 0 to 5:

English Language  4.5 / 5
0
5
Law and Government  4.1 / 5
0
5
Biology  3.5 / 5
0
5
Computers and Electronics  3.4 / 5
0
5
Administration and Management  3.4 / 5
0
5
Administrative  3.2 / 5
0
5

Abilities

The abilities that matter most for regulatory affairs specialists, rated on an importance scale of 0 to 5:

Written Comprehension  4.2 / 5
0
5
Written Expression  4.1 / 5
0
5
Oral Comprehension  4.0 / 5
0
5
Oral Expression  4.0 / 5
0
5
Inductive Reasoning  3.9 / 5
0
5
Problem Sensitivity  3.9 / 5
0
5

Daily Tasks

Common tasks include:

  • Coordinate efforts associated with the preparation of regulatory documents or submissions.
  • Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review.
  • Prepare or direct the preparation of additional information or responses as requested by regulatory agencies.
  • Coordinate, prepare, or review regulatory submissions for domestic or international projects.
  • Prepare or maintain technical files as necessary to obtain and sustain product approval.
  • Interpret regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures.
  • Determine the types of regulatory submissions or internal documentation that are required in situations such as proposed device changes or labeling changes.
  • Coordinate recall or market withdrawal activities as necessary.
  • Advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues.
  • Review adverse drug reactions and file all related reports in accordance with regulatory agency guidelines.
  • Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.
  • Identify relevant guidance documents, international standards, or consensus standards.

Work Activities

  • Evaluating Information to Determine Compliance with Standards
  • Getting Information
  • Communicating with Supervisors, Peers, or Subordinates
  • Communicating with People Outside the Organization
  • Working with Computers
  • Making Decisions and Solving Problems
  • Interpreting the Meaning of Information for Others
  • Updating and Using Relevant Knowledge
  • Establishing and Maintaining Interpersonal Relationships
  • Analyzing Data or Information
  • Organizing, Planning, and Prioritizing Work
  • Developing Objectives and Strategies

Tools & Technology

Common tools and software used in this occupation include: Hot technologies: Adobe Acrobat, Microsoft Access In-demand technologies: Microsoft Excel

What Major Will Prepare You For This Career?

Programs that train for this career include:

Careers similar to regulatory affairs specialists include:

Also Known As

Anti Money Laundering Compliance Analyst (AML Compliance Analyst), CMC Regulatory Affairs Manager (Chemistry, Manufacturing, and Controls Regulatory Affairs Manager), Clinical Quality Assurance Associate, Clinical Quality Assurance Specialist, Drug Regulatory Affairs Specialist, Product Safety Specialist, Product Stewardship Specialist, Quality Assurance Documentation Coordinator, Quality Assurance Documentation Specialist, Regulatory Affairs Analyst (RA Analyst), Regulatory Affairs Associate (RA Associate), Regulatory Affairs Consultant (RA Consultant), Regulatory Affairs Coordinator (RA Coordinator), Regulatory Affairs Scientist, Regulatory Affairs Specialist (RA Specialist).

References

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