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Mv01 - 022326 Validation & Supplier Qualification Tech Support

Own our supplier qualification and validation protocol execution across regulated manufacturing environments
Mid-Level
yesterday
Validation & Engineering Group

Validation & Engineering Group

A provider of engineering, commissioning, and validation services for the pharmaceutical, biotechnology, and medical device industries.

2 Similar Jobs at Validation & Engineering Group

Validation & Engineering Group, Inc. (V&EG) A Pinnaql Company

V&EG, a Pinnaql company, is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

Job Title: Validation & Supplier Qualification Tech Support

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Description:

  • Execution and technical documentation of IQ/OQ/PQ validations, including protocol development, final reports, and statistical analysis of results.
  • Hands-on experience in Process Validation, Equipment Qualification, and Computer System Validation (CSV) in compliance with FDA 21 CFR Part 820, ISO 13485, and cGMP requirements.
  • Development and execution of Supplier Qualification, including technical audits, process capability analysis (Cp, Cpk), and risk assessment under ISO 14971.
  • Technical investigation of deviations and non-conformances, applying Root Cause Analysis tools (5 Whys, Fishbone) and supporting CAPA implementation.
  • Technical support for product transfers, engineering changes (ECO/ECN), and revalidation of critical processes.

Qualifications:

  • Bachelor's Degree in Engineering or Science.
  • Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.
  • Experience in direct process / manufacturing areas.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test (SAT).
  • Technical Writing skills and investigations processes.
  • Available to work extended hours, possibility of weekends and holidays.
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Mv01 - 022326 Validation & Supplier Qualification Tech Support
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About Validation & Engineering Group
A provider of engineering, commissioning, and validation services for the pharmaceutical, biotechnology, and medical device industries.