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Skills
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Change Controlunmatched
Chemistryunmatched
Code of Federal Regulationsunmatched
Commissioningunmatched
Computer Systemsunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Data Qualityunmatched
ERP (Enterprise Resource Planning)unmatched
Equipment Validationunmatched
External Auditunmatched
FDA (Food and Drug Administration)unmatched
GMP (Good Manufacturing Practices)unmatched
GxPunmatched
Internal Auditunmatched
Laboratory Information Management System (LIMS)unmatched
Maintain Complianceunmatched
Manufacturing Automationunmatched
Manufacturing Systemsunmatched
Mentoringunmatched
Pharmacyunmatched
Process Validationunmatched
Programmable Logic Controller (PLC)unmatched
Quality Assuranceunmatched
Regulationsunmatched
Risk Analysisunmatched
Sales Qualificationunmatched
Supervisory Control and Data Acquisition (SCADA)unmatched
System Validationunmatched
Technical Writingunmatched
Validation Documentationunmatched
Validation Planunmatched
Writing Skillsunmatched
Description
Job Description:
We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. The ideal candidate will be responsible for planning, executing, reviewing, and approving validation documentation for equipment, facilities, utilities, processes, and computerized systems while ensuring compliance with FDA, EMA, and cGMP regulations. Responsibilities:
Lead validation lifecycle activities including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Author, review, and approve validation protocols, reports, risk assessments, and validation plans.
Execute equipment, process, cleaning, utility, facility, and computer system validation activities.
Support commissioning and qualification (C&Q) activities for new equipment and manufacturing systems.
Manage deviations, investigations, CAPAs, and change controls related to validation activities.
Develop and maintain Validation Master Plans (VMPs).
Ensure compliance with cGMP, GxP, FDA, EU GMP, and data integrity requirements.
Support regulatory inspections and internal/external audits.
Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, and Regulatory teams.
Mentor junior validation engineers and specialists.
Requirements:
Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related field.
5+ years of validation experience in a GMP-regulated environment.
Strong knowledge of:
IQ/OQ/PQ
Process Validation
Equipment Qualification
Cleaning Validation
Computer System Validation (CSV)
Risk Assessments
Change Control and CAPA
Experience with FDA, EMA, 21 CFR Part 11, and GAMP 5 guidelines.
Excellent technical writing and documentation skills.
Preferred Qualifications:
Experience with MES, LIMS, SCADA, PLC, ERP, or other GMP computerized systems.
Knowledge of Kneat, ValGenesis, TrackWise, MasterControl, or similar validation tools.
Experience supporting audits and regulatory inspections.
Validation certification or advanced degree preferred.