About this role

Company Description

Validation & Engineering Group, Inc.Β (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.

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Job Description

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

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.

Additional Information

Frequently Asked Questions

Is the salary disclosed for the Validation Engineer Lead position at validationengineeringgroup?
The salary for this Validation Engineer Lead role at validationengineeringgroup is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Validation Engineer Lead position at validationengineeringgroup located?
This Validation Engineer Lead role at validationengineeringgroup is based in Juncos, Juncos, , Puerto Rico, pr. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Validation Engineer Lead role at validationengineeringgroup full-time or part-time?
This is listed as a Full time position. It is posted as a Validation Engineer Lead role at validationengineeringgroup.
How do I apply for the Validation Engineer Lead position at validationengineeringgroup?
Click the "Apply Now" button on this page. You will be redirected to validationengineeringgroup's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the Validation Engineer Lead job at validationengineeringgroup posted?
This Validation Engineer Lead position at validationengineeringgroup was posted on Nov 10, 2025. Apply as soon as possible β€” early applications are often reviewed first.
Validation Engineer Lead
validationengineeringgroup
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