Validation & Supplier Qualification Tech Support

Validation and Engineering Group, Inc

Posted on: March 27, 2026

Closing: April 26, 2026

Salary: Undisclosed

Job Description

Validation & Engineering Group, Inc. (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.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Validation & Supplier Qualification Tech Support

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.

Validation and Engineering Group, Inc

Posted on: March 27, 2026

Closing: April 26, 2026

Salary: Undisclosed

Career Focus: Validation

This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.

Similar Jobs


Colorado, United States

Validation Engineer I – Project...

When joining PerkinElmer, you select an experienced and trusted leader i...

King of Prussia, Pennsylvania, United States

Process Validation Engineer

Process Validation Engineer (a minimum of 5 years of experience required...

Western Springs, Illinois, United States

Commissioning, Qualification & Validation Consultant...

For the past 20 years, ProPharma has improved the health and wellness of...

Billerica, Massachusetts, United States

Validation Engineer II

Job Summary Validation Engineer II is expected to execute validation and...