Validation (CQV) Engineer

BioPharma Consulting JAD Group; College Station, Northern (TX, KY); On-site; USD 90,000 - 130,000; Full time

Job summary

BioPharma Consulting JAD Group is seeking a Validation Engineer to provide scientific and technical support for product launches, technology transfers, and new technologies at the FDBT site. The role emphasizes right‑first‑time execution, compliance, and continuous improvement.

You will execute key validation lifecycle activities (CD, CQ, PQ, PR) and collaborate with cross‑functional teams, vendors, and network partners.

Qualifications

• On-site role; remote work is not permitted.
• Experience creating full validation lifecycle documentation (URS, FRS, DS, engineering specifications)
• Strong understanding of validation processes and regulatory requirements
• Ability to independently troubleshoot, resolve, and communicate technical issues
• Proven experience leading cross‑functional teams and coordinating complex projects
• Ability to develop and manage detailed IQ/OQ/PQ/RQP execution plans
• Working knowledge of Computerized Systems Validation (CSV)
• Support implementation of new process technologies aligned with regulatory needs
• Vendor validation activities oversight and deviation reporting
• Willingness to work holidays and weekends

Responsibilities

• Provide scientific and technical support for product launches and technology transfers
• Execute key validation lifecycle activities (CD, CQ, PQ, PR)
• Collaborate with cross‑functional teams and network partners
• Develop and maintain validation documentation (protocols, reports)
• Ensure right‑first‑time execution, compliance and continuous improvement
• Mentor and guide junior team members
• Assist in implementing new process technologies
• Review and approve vendor protocols and deviation reports
• Coordinate sample collection and data retrieval per protocol requirements
• Prepare summary reports for validation activities

Skills

Cross-functional leadership

Project planning

Troubleshooting

Documentation writing

Regulatory understanding

Independent work

Mentoring juniors

Education

Bachelor’s degree in Engineering or Science

Tools

Kneat

MS Word

MS Excel

MS PowerPoint

Job description

The Validation Engineer is responsible for providing scientific and technical support for product launches, technology transfers, and new technology introductions at the FDBT site. This role executes key validation lifecycle activities—including Cycle Development (CD), Commissioning & Qualification (CQ), Performance Qualification (PQ), and Periodic Reviews (PR)—while collaborating closely with cross‑functional teams across the site and occasionally with network partners. Emphasis is placed on right‑first‑time execution, compliance, and continuous improvement.

Key Requirements

• On‑site role; remote work is not permitted.
• Experience creating full validation lifecycle documentation:
  • URS, FRS, DS, engineering specifications
  • Validation protocols (VPP, IQ, OQ, PQ)
  • System Impact Assessments, Requirements Traceability Matrix, Final Reports
• Strong understanding of validation processes and regulatory requirements.
• Ability to independently troubleshoot, resolve, and communicate technical issues.
• Proven experience leading cross‑functional teams and coordinating complex projects.
• Ability to develop and manage detailed project plans and timelines for IQ/OQ/PQ/RQP execution.
• Working knowledge of Computerized Systems Validation (CSV).
• Support implementation of new process technologies aligned with business and regulatory needs.
• Ownership of vendor‑performed validation activities, including:
  • Review and approval of vendor protocols
  • Issue resolution
  • Validation deviation reporting
  • Summary report generation
• Coordinate and execute tactical validation activities:
  • Sample collection
  • Data retrieval
  • Documentation completion per protocol requirements
• Excellent technical writing skills for SOP creation and updates.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Ability to work independently, multitask, and support multiple projects simultaneously.
• Provide guidance and support to junior team members.
• Must be available to work as needed, including holidays and weekends.

Areas of Expertise

• Kneat electronic validation documentation
• Data loggers (pre/post calibration procedures)
• Temperature mapping: cold rooms, freezers, refrigerators, incubators
• Laboratory equipment (e.g., Mass Photometer)
• Autoclaves & cycle development
• EMPQs
• Biowelders
• Culture chemistry analyzers
• Smoke studies
• Fillers
• VHP decontamination & cycle development
• Bioquell Qube
• Mixers, tanks, VCells
• AKTA systems
• Filter integrity testers
• Pumps
• Centrifuges
• Downflow hoods
• Weight scales
• SME Water Systems (WFI, RODI)
• Clean gas utilities
• Facilities systems

Education Requirements

• Bachelor’s degree in Engineering or Science (minimum).
• 7+ years of validation experience in the life sciences industry.

• Administrative shift
• 1-year contract with possible extension