Senior Validation Engineer

Crystal Equation Corporation

📍 thousand oaks, ca, United-States

Full-time Pharmaceutical Manufacturing

Job Description

Summary

Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating/reviewing/executing C&Q protocols, plans, and summary reports. Works with project teams and SMEs to develop testing strategies. Participates in project meetings to inform stakeholders on progress of C&Q activities.


Responsibilities

  • Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines.
  • Work with project teams to develop the commissioning and qualification strategy and document in qualification plans.
  • Generate/evaluate qualification/validation protocols including IQ, OQ, FT, PQ protocols and final reports for new or modified GMP analytical and process equipment, utilities, and facilities.
  • Execute IQ, OQ, FT, P...
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