Validation Engineer/Specialist (Atlanta, Georgia)

Validation & Engineering Group

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Duluth, GA, us on site Until 8/22/2026 First posted March 27, 2025 Last posted March 27, 2025
Job description

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

  • Expertise in “Risk Based Approach” for Commissioning and Qualification practices
  • Planning and Integration of Commissioning and Qualification activities in medical device manufacturing (Class II preferred)
  • Risk Management practices (i.e. Assessments, Functional Risk Documents, pFMEA, etc.)
  • Equipment qualification and process validation
  • Computerized System Validation (PLC, HMI, etc.)
  • 21 CFR Part 11 requirements and how to incorporate these requirements into an efficient testing strategy
  • Assist in deviation investigation and resolution for problems and issues encountered during field execution activities

Education:

  • B.S. Engineering (e.g. Computer Science, Chemical, Mechanical, Electrical, etc.)

Minimum Skills:

  • 3-5 years hands-on validation experience (writing and execution of validation protocols)
  • Capable of working independently with minimal supervision, and communicating with project team members to assure timelines are met
  • Great technical writing and communication skills
  • Proficiency in Microsoft Office application (Word, Excel and Project)
  • Effective interpersonal and problem solving skills
  • Demonstrate excellence in good documentation requirements and attention to detail

Positions available for Puerto Rico.

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.

About this role

Summary

Perform validation activities for medical devices, including risk management, equipment qualification, and computer validation.

Job title

Validation Engineer/Specialist

Experience level

3-5 years

Industry

pharmaceutical

Location requirements

Duluth, GA, US; remote work not specified

Salary

Not specified

Management role

No

Skills & keywords

Required skills

validation protocolsrisk managementequipment qualificationcomputerized system validation21 CFR Part 11technical writing

Preferred skills

project managementgood documentation

Specializations

risk managementequipment qualificationcomputerized system validationmedical devices
Locations

Structured locations inferred from the posting.

Duluth, GA, USA

On-site City