Validation Specialist
About The Position
EQVAL Group, Inc. is a company that provides technical and engineering services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies) and other service companies. We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, to perform and provide a highly effective service. Validation Specialist (Short-Term Contract – 3 Months) 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.
Requirements
- 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).
- Knowledge of QC laboratory requirements for equipment qualification.
- Experience working with laboratory equipment and controlled temperature equipment.
- Experience using data loggers for temperature monitoring.
Nice To Haves
- 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.
Benefits
- Paid time off
- Health insurance
- Dental insurance
- Vision insurance
- Life insurance
- Employee assistance program
- Employee discount
- Professional development (certifications, courses & assistance)
- Referral program
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What This Job Offers
Career Level
Entry Level
