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Regulatory Affairs
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Thanks for your interest in the Regulatory Affairs Specialist (A Global Regulatory Affairs Lead Role - GRAL) Open in all the countries in Latin America position. Unfortunately this position has been closed but you can search our 0 open jobs by clicking here.
 
Education and Experience:
  • Bachelor's Degree in Pharmacy or Life Science
  • 2-3 years regulatory experience, or combination of higher education/less experience
  • Or substitution of equivalent relevant work experience
 
Knowledge, Skills and Abilities:
  • Broad regulatory affairs experience
  • Good interpersonal skills
  • Good knowledge Global Regulatory Affairs Procedures
  • Proven ability to work effectively in a team
  • A good knowledge of a number of country specific clinical trial application procedures Expert knowledge of ICH and global regulatory guidelines
  • Familiar with computers and their applications
  • Good organizational and planning skills
  • Must be able to work autonomously with minimal supervision
  • Planning skills
  • Mental skills required in areas of reading and interpretation of data, numeracy, language, analytical, investigative, verbal and written communication, customer contact, attention to detail, multiple project tasking

 

Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.