Process Validation, Equipment Qualification :: Global Validation

Employment Opportunities

Validation Specialist

*Job Summary*


*Required Skills*

- Bachelor’s Degree in Engineering or Life Sciences - Up to four (4) years of experience related to the Validation field in the Pharmaceutical, Medical Devices and/or Biotechnology Industries - Must be fully bilingual (English/Spanish) and must demonstrate excellent written skills, especially in the preparation of technical reports - Proficiency in Windows and Microsoft Office applications - Ability in analyzing and generating data - Ability to perform the assigned work on schedule, quality, and budget - Initiative, Motivation and Organization - Good interpersonal skills - Willing to travel
*Desired Skills*

- Demonstrate strong understanding of cGMPs regulatory environment - Knowledge in Validation/Qualification Documentation such as: Master Plan, Design Reviews, Protocols, Reports, Investigations, Deviations, CSV Life Cycle Documents, and SOPs - Knowledge in Validation/Qualification Execution - Knowledge in PC and PLC technical skills - Knowledge in Good Documentation Practices - Ability to work with minor supervision - Self-starter and good team player - Leadership skills - Highly adaptable to changes in priority - Customer service oriented - Safety awareness - Able to maintain confidentiality