Validation Specialist

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 a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

We are looking for a qualified Jr. Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing:

• Validation protocols.
• Validation reports.
• SOPs (Standard Operating Procedures).
• Statistical data analysis

Qualifications

• Bachelor in Sciences with 2 years of experience in a GMP environment preferably in the pharmaceutical industry
• Ability to work on multidisciplinary projects and comply with regulatory requirements.
• Experience with aseptic and regulated processes and developing and executing:Validation protocols, Validation reports, and SOPs (Standard Operating Procedures).
• Statistical data analysis
• Bilingual (English and Spanish)

Additional Information

All your information will be kept confidential according to EEO guidelines.

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