Junior Validation Specialist: Aseptic Pharma GMP

QRC Group, Inc; Aibonito (PR); On-site; USD 42,000 - 60,000; Full time

Job summary

QRC Group, LLC is seeking a Jr. Validation Specialist to join our team. The role focuses on aseptic and regulated processes and the development and execution of validation protocols, validation reports, and SOPs.

The ideal candidate has a Bachelor in Sciences and at least 2 years of GMP experience, with proficiency in statistical data analysis and bilingual English/Spanish abilities. Join a collaborative environment dedicated to regulatory excellence in the pharmaceutical industry.

Qualifications

• Bachelor in Sciences with 2 years of GMP experience in a pharma setting.
• Ability to work on multidisciplinary projects and meet regulatory requirements.
• Experience with aseptic and regulated processes and developing and executing validation protocols, reports, and SOPs.
• Statistical data analysis.
• Bilingual English and Spanish.

Responsibilities

• Develop and execute validation protocols.
• Prepare validation reports.
• Create and update SOPs.
• Perform statistical data analysis.

Skills

Validation protocols

Validation reports

SOPs

Statistical data analysis

Education

Bachelor in Sciences

Job description

QRC Group, LLC is seeking a Jr. Validation Specialist to join our team. The role focuses on aseptic and regulated processes and the development and execution of validation protocols, validation reports, and SOPs.

The ideal candidate has a Bachelor in Sciences and at least 2 years of GMP experience, with proficiency in statistical data analysis and bilingual English/Spanish abilities. Join a collaborative environment dedicated to regulatory excellence in the pharmaceutical industry.