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Associate Validation & Qualification - Level 3

Guayama, PR · Biotech/Pharmaceutical

KEY RESPONSIBILITIES

  • Perform, Qualification life cycle
  • Protocol & Report
  • Change Control Generation
  • Troubleshooting
  • Experience in GMP workplace.
  • Experience in Manufacturing and Packaging equipment

QUALIFICATIONS

  1. Bachelor's degree in Engineering, Life Sciences, or related field.
  2. Experience executing the full Qualification Life Cycle, including protocol preparation, execution, and reporting.
  3. Ability to generate and complete Protocols and Reports aligned with GMP and validation standards. 
  4. Experience in Change Control generation and management within a GMP-regulated environment.
  5. Proven troubleshooting skills during validation and qualification activities.
  6. Hands-on experience working in a GMP-regulated workplace, with understanding of compliance expectations.
  7. Practical experience with Manufacturing equipment and processes, including hands-on involvement in system qualifications.
  8. Practical experience with Packaging equipment, including qualification or support roles.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*

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