Descripción del Empleo:
The Quality Inspector is a member of the Quality Unit assigned to assure compliance with Current Good Manufacturing Practices (CGMP) at different operational areas of the pharmaceutical operations.

Major Areas of Responsibility:
Comply and oversee the compliance with:
• CGMP.
• Standard Operating Procedures (SOP)
• General Documentation Practices (GDP)
Requisitos:
Primary Objectives: Warranty the quality attribute of the manufactured products by ensuring throughout the manufacturing operations compliance with CGMP’s.

Required Knowledge, Skills, and Abilities:
• Job Requirements
o Associate Degree or 2 years of studies in an accredited collage/university with 3 years of experience in a Good Manufacturing Practices environment or equivalent in work experience.
o Knowledge in Good Documentation Practices
o Read and understand written instructions in English
o Capacity of inspect and identify deficiencies in documents and processes
o Capacity to work stand up and in continuous movement through the assigned areas about 80% of the time
o Capable to handle materials with weight over 25 pound (when needed)
o Leadership
o Must be able to perform and comple