Entry-Level Validation Engineer & CQV Associate | Onsite

RXinsider LTD.; Phoenix (AZ); On-site; USD 60,000 - 80,000; Full time

Job summary

Medivant Healthcare, a U.S.-based pharmaceutical manufacturer with FDA-registered facilities in Chandler and Deer Valley, AZ, is seeking an entry-level Validation Engineer and CQV Associate. The role supports validation documentation, data collection, and quality system activities in a sterile injectable facility.

Ideal for recent graduates seeking hands-on cGMP and aseptic processing experience; training provided.

Qualifications

• Bachelor's degree in Pharmacy, Biotechnology, Microbiology, Life Sciences, or related field.
• 2-3 years of relevant experience is required
• Understanding of aseptic and sterile processing.
• Strong documentation and communication skills.

Responsibilities

• Assist in execution of validation studies and documentation.
• Support area qualification and environmental monitoring tasks.
• Draft IQ/OQ/PQ protocols and assist execution.
• Collect data for HVAC, WFI, and compressed air validation.
• Assist in cleaning validation logs and sample documentation.
• Participate in process validation protocol preparation.
• Support change control documentation.
• Assist in deviation data collection and preliminary reports.
• Track CAPA activities and closure evidence.

Skills

Documentation skills

Communication skills

Education

Bachelor's degree in Pharmacy Biotechnology Microbiology Life Sciences or related field

Job description

Medivant Healthcare, a U.S.-based pharmaceutical manufacturer with FDA-registered facilities in Chandler and Deer Valley, AZ, is seeking an entry-level Validation Engineer and CQV Associate. The role supports validation documentation, data collection, and quality system activities in a sterile injectable facility.

Ideal for recent graduates seeking hands-on cGMP and aseptic processing experience; training provided.