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The Validation Specialist will support validation and daily laboratory activities in a Medical Device regulated environment. This role is responsible for ensuring laboratory equipment and systems are properly qualified and compliant with applicable regulatory requirements.
Qualifications:
Bachelor’s Degree in Chemistry, Microbiology, Engineering, or a related scientific field.
3–5 years of experience in a laboratory environment within the Medical Device, Pharmaceutical, or Biotechnology industry.
Experience with laboratory equipment validation, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Experience validating laboratory equipment such as FTIR spectrophotometers for identification, endotoxin testing equipment (e.g., Nebula), and laboratory freezers is preferred.
Experience with Computer System Validation (CSV) for laboratory systems is preferred.
Knowledge of QC laboratory requirements for equipment qualification.
Benefits:
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