Senior Validation Engineer – Pharma Systems & Compliance

Barry-Wehmiller Companies Inc.

Columbia (MD)

Hybrid

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Barry-Wehmiller Companies Inc. is seeking a Validation Engineer III in Columbia, MD to support capital projects by developing and executing validation and FDA compliance documents for pharmaceutical equipment.

The role involves travel to top clients and collaboration with cross-functional teams to implement robust validation strategies and deliver high-quality results. The ideal candidate has 7+ years in validation of automation, packaging, utilities or facilities, plus 3+ years in

Qualifications

  • Strong communication and interpersonal skills.
  • 7+ years of project experience with validation of automation, packaging, utilities and/or facilities.
  • 3+ years of project experience in pharmaceutical or medical device environments is a plus.
  • Strong technical writing ability.
  • Solid computer skills (MS Office, MS Project, AutoCAD).
  • Willingness to travel for project needs.

Responsibilities

  • Develop and execute validation and FDA-compliance documents/protocols for pharmaceutical equipment.
  • Travel to top clients across the country to assist design of manufacturing processes and manage projects.
  • Develop and execute FAT, SAT, IQ and OQ documentation on automated systems.
  • Contribute to development and execution of quality management system procedures (ICH/Q8–Q10) and regulatory standards.
  • Investigate and troubleshoot validation issues and prepare written validation reports.
  • Collaborate with teams to deliver high-quality validation solutions to clients.

Skills

Communication
Interpersonal skills
Technical writing
Microsoft Office
AutoCAD
Travel readiness

Education

BS in Bioengineering / Biomedical Engineering / Chemical Engineering

Tools

Microsoft Project
AutoCAD

Job description

Barry-Wehmiller Companies Inc. is seeking a Validation Engineer III in Columbia, MD to support capital projects by developing and executing validation and FDA compliance documents for pharmaceutical equipment.

The role involves travel to top clients and collaboration with cross-functional teams to implement robust validation strategies and deliver high-quality results. The ideal candidate has 7+ years in validation of automation, packaging, utilities or facilities, plus 3+ years in

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