image
  • Snapboard
  • Activity
  • Reports
  • Campaign
Welcome ,
loadingbar
Loading, Please wait..!!

MV01-022326 Validation & Supplier Qualification Tech Support

  • ... Posted on: Feb 22, 2026
  • ... Validation & Engineering Group, Inc
  • ... 00983, null
  • ... Salary: Not Available
  • ... Full-time

MV01-022326 Validation & Supplier Qualification Tech Support   

Job Title :

MV01-022326 Validation & Supplier Qualification Tech Support

Job Type :

Full-time

Job Location :

00983 null United States

Remote :

No

Jobcon Logo Job Description :

Job Description

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.

View Full Description

Jobcon Logo Position Details

Posted:

Feb 22, 2026

Reference Number:

04f992e6

Employment:

Full-time

Salary:

Not Available

City:

00983

Job Origin:

ziprecruiter

Share this job:

  • linkedin

Jobcon Logo
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

MV01-022326 Validation & Supplier Qualification Tech Support    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Job Description

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.

Loading
Please wait..!!