Pharma Validation Specialist – GMP, Microbiology & USP

Mindlance; Collegeville (PA); Presencial; USD 65.000 - 85.000; Jornada completa

Descripción de la vacante

A national recruiting company is seeking a candidate for a role involving validation protocols within the pharmaceutical industry. Responsibilities include writing validation protocols, executing them in collaboration with support groups, and preparing regulatory documentation. Ideal applicants should have a Bachelor's degree in a scientific field and proven experience in microbiological testing validation. Strong initiative and a solid understanding of validation principles and FDA regulations are essential for success in this role.

Formación

• Bachelor's degree in a relevant field such as Biology, Microbiology, or Engineering.
• Proven experience in validation within the pharmaceutical industry.
• Strong initiative and understanding of validation principles and FDA requirements.

Responsabilidades

• Write and coordinate validation protocols and reports.
• Execute validation protocols with support groups.
• Prepare documentation for regulatory filings.

Conocimientos

Validation protocols writing

Microbiological testing validation

GMP laboratory operations

Knowledge of FDA regulations

Understanding of validation principles

Educación

Bachelor’s degree in a scientific or technical discipline

Descripción del empleo

A national recruiting company is seeking a candidate for a role involving validation protocols within the pharmaceutical industry. Responsibilities include writing validation protocols, executing them in collaboration with support groups, and preparing regulatory documentation. Ideal applicants should have a Bachelor's degree in a scientific field and proven experience in microbiological testing validation. Strong initiative and a solid understanding of validation principles and FDA regulations are essential for success in this role.