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Validation & Engineering Group

Life sciences validation and compliance consulting

Validation Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRaleigh, NC, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Engineering, Life Sciences, or a related field.
  • At least 5 years of validation experience in the pharmaceutical, biotechnology, or a related regulated industry.
  • Hands-on experience validating manufacturing equipment, laboratory instruments, and/or computerized systems.
  • Strong knowledge of Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and regulatory guidelines.
  • Strong analytical, organizational, and technical writing skills.
  • Ability to work independently and in cross-functional teams.

Responsibilities

  • Plan, develop, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) validation protocols for equipment, utilities, facilities, and manufacturing systems.
  • Support validation of laboratory instruments, production equipment, cleaning processes, and computerized systems.
  • Ensure compliance with current Good Manufacturing Practice (cGMP), the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA), and other applicable regulatory guidelines.
  • Draft and review validation documentation, including protocols, reports, standard operating procedures (SOPs), and risk assessments.
  • Perform troubleshooting and root cause analysis for validation or equipment-related deviations.
  • Collaborate with Engineering, Quality, Manufacturing, and Laboratory teams to support project deliverables.
  • Participate in change control, Corrective and Preventive Action (CAPA), and continuous improvement initiatives.
  • Maintain accurate records and ensure documentation is audit-ready at all times.

Desired Qualifications

  • Experience with cleaning validation, sterilization, and utilities such as heating, ventilation, and air conditioning (HVAC), water, and compressed gases.
  • Familiarity with data integrity and 21 CFR Part 11 compliance.
  • Knowledge of risk-based validation approaches such as ASTM E2500.

About the Company

Validation & Engineering Group

Life sciences validation and compliance consulting

Validation & Engineering Group provides regulatory compliance and engineering consulting for life sciences clients in Puerto Rico and the USA, serving pharma, biotechnology, medical devices, and food sectors. It guides the full product lifecycle, performing commissioning and qualification, computer system, equipment, process, and cleaning validation, drafting quality systems, and ensuring regulatory compliance with FDA and European standards. The firm differentiates itself with hands-on engineering expertise combined with deep regulatory knowledge and broad geographic reach, now enhanced after joining Pinnaql Inc. through an acquisition by 3Boomerang Capital, with founders continuing as partners for continuity. Its goal is to help clients bring products to market faster and more reliably by sustaining GMP-compliant operations and ongoing lifecycle compliance.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Guaynabo, Puerto Rico
Founded
1997

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