Validation Engineer Lead

Validation & Engineering Group

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Juncos, pr on site Until 8/21/2026 First posted November 11, 2025 Last posted November 11, 2025
Job description

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.

 

Key Responsibilities:

  • Develop, review, and execute commissioning and qualification protocols (IQ/OQ/PQ) for downstream processing equipment.
  • Coordinate FAT/SAT execution and documentation with vendors and engineering teams.
  • Perform field inspections, loop checks, and functional verifications during commissioning.
  • Ensure equipment is installed and operates per design specifications, user requirements, and cGMP standards.
  • Support resolution of deviations and discrepancies identified during commissioning and qualification.
  • Author and/or review commissioning plans, traceability matrices, risk assessments, and validation summary reports.
  • Interface with validation, manufacturing, automation, and QA to ensure alignment and timely execution of CQV activities.
  • Participate in change control evaluations and equipment impact assessments.

Downstream Equipment in Scope:

  • Chromatography Skids.
  • Tangential Flow Filtration (TFF) systems.
  • Depth filtration units.
  • Centrifuges and continuous flow centrifuges.
  • Virus filtration and inactivation systems.
  • Bulk product hold tanks and transfer skids.
  • Clean-in-place (CIP) and Steam-in-place (SIP) systems.

Qualifications:

  • Bachelor’s degree in engineering, biotechnology, or related life sciences discipline.
  • 3–7 years of CQV experience in a GMP-regulated biotech or pharmaceutical environment.
  • Strong understanding of downstream unit operations and associated automation.
  • Proficient in writing and executing validation protocols and working within electronic validation systems (e.g., Valgenesis, Kneat).
  • Familiarity with FDA, EMA, and ICH guidelines.
  • Excellent communication and documentation skills.

Preferred Skills:

  • Experience with single-use technologies (SUT) in downstream processing.
  • Knowledge of DeltaV, Rockwell, or Siemens PLC-based automation systems.
  • Experience working on greenfield or facility expansion projects.
About this role

Summary

Develop and execute validation protocols for biotech equipment, ensuring compliance with GMP standards.

Job title

Validation Engineer Lead

Experience level

3-7 years

Industry

pharmaceutical

Location requirements

Juncos, PR; remote work not specified

Salary

Not specified

Management role

No

Skills & keywords

Required skills

validation protocolsCQVGMPautomationelectronic validation systems

Preferred skills

single-use technologiesDeltaVRockwellSiemens PLCfacility expansion

Specializations

CQVdownstream processingvalidation protocolsautomationGMP
Locations

Structured locations inferred from the posting.

Juncos, 00777, Puerto Rico

On-site City