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MVSr Validation Specialist

Job in Indianapolis, Marion County, Indiana, 46262, USA
Listing for: Veg Group
Full Time position
Listed on 2025-11-04
Job specializations:
  • Engineering
    Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
MV01-080725 Sr Validation Specialist (IN)

Validation & Engineering Group, Inc. (V&EG) 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:

  • Senior Validation Engineer

Job Summary:

Hands on CQV/validation work supporting device assembly and automation projects for a combination autoinjector product. Ideal candidates will bring a strong cGMP background and experience with automated systems, packaging, and FMEAs.

Key Responsibilities:

  • Lead or support CQV activities for equipment, utilities, and processes in accordance with cGMP and client procedures (including IQ/OQ/PQ).
  • Oversee design and process FMEA development and execution.
  • Support assembly, packaging, and automation equipment qualification related to autoinjector devices.
  • Participate in vendor reviews, FATs/SATs, and tech transfers (including international travel).
  • Collaborate with cross-functional teams including engineering, quality, automation, and project management.
  • Ensure compliance with applicable regulatory and quality standards (FDA, EMA, ISO 13485, 21 CFR Part
    4).
  • Review and approve technical documentation such as validation protocols, reports, and risk assessments.
  • Interface with stakeholders to support project planning, scheduling, and execution.

Qualifications:

  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • 5+ years of experience in CQV, validation, or technical operations within regulated environments.
  • Strong knowledge of cGMPs, validation lifecycle, and regulatory expectations.
  • Proven experience with combination products, preferably autoinjector platforms.
  • Hands-on experience with automated device assembly equipment, vision systems, and packaging machinery.
  • Experience with DFMEA/PFMEA methodologies.
  • Willingness to travel internationally for vendor engagements.
  • Excellent written and verbal communication skills.
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