JT139 - VALIDATION SPECIALIST

Quality Consulting Group-posted 3 months ago
PR
51-100 employees
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QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic individual to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

  • Developing, executing, and documenting validation protocols, deviations, and reports to meet company and regulatory requirements.
  • Collaboration with cross-functional teams—including Quality, Manufacturing, and Maintenance—to plan, coordinate, and execute validation activities while ensuring efficient use of time and resources.
  • Maintain accurate records, adhere to safety guidelines during validations, and support investigations or issue resolution related to validation activities.
  • Bachelor’s degree
  • 2 years of relevant experience
  • Generation and execution of equipment validation.
  • Hands-on experience with equipment and process validation in a regulated industry.
  • Basic knowledge of statistical tools which are used for sampling determination, and process characterization.
  • Proven ability to manage validation documentation and meet deadlines.
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