Reckitt · 8 hours ago
Validation Specialist
Reckitt is a global leader in hygiene, health, and nutrition brands dedicated to creating a cleaner, healthier world. The QA Validation Specialist is responsible for ensuring that equipment, systems, and processes meet regulatory and internal quality standards through validation and qualification activities in a GMP-compliant pharmaceutical environment.
Cleaning ProductsHealth CareHome Health CareManufacturingMedicalProduct Design
Responsibilities
Define scope, objectives, and strategy for validation activities aligned with regulatory and quality standards
Develop and review IQ/OQ/PQ protocols for equipment, utilities, and manufacturing processes
Ensure compliance with FDA, EMA, ICH, and internal quality systems
Maintain validated state through periodic reviews, requalification, and change control
Partner with Engineering and Validation teams to ensure GMP‑compliant equipment design, installation, and operation
Participate in risk assessments (FMEA, HAZOP) to identify and mitigate quality and compliance risks
Review change controls, equipment specs, and commissioning documentation
Promote consistent validation practices through coaching and hands‑on support
Ensure validation documentation meets data integrity and regulatory expectations
Maintain accurate, complete records per SOPs and quality standards
Support audits by providing validation documentation and SME input
Investigate validation deviations and non‑conformances
Support root cause analysis and CAPA implementation
Collaborate with QA, QC, Regulatory, Engineering, and Manufacturing teams
Provide guidance on validation best practices and compliance requirements
Ensure GxP documents are current, approved, accessible, and aligned with digital documentation practices
Support development and sustainability of training systems for the new production site
Maintain new‑hire orientation materials and drive training improvements
Generate reports and support training initiatives
Assign, monitor, and communicate training requirements
Identify and drive continuous improvement in validation processes to enhance quality, reduce costs, and optimize service delivery
Qualification
Required
Bachelor's degree in Life Sciences, Engineering, or related field
3+ years of validation experience in a pharmaceutical environment
Skilled in risk‑based validation and quality systems
Proficient with Microsoft Office and validation software tools
Strong analytical, documentation, and communication abilities
Effective cross‑functional collaborator with validation project experience
Knowledge of FDA, EMA, ICH Q7–Q10, GAMP 5, and data integrity principles
Experience leading small high‑performing teams and removing barriers to success
Familiar with enterprise systems (Veeva Vault, SAP, PAS‑X)
Experience with validated systems and CSA/data integrity requirements
Hands‑on LEAN experience (VSM, Kaizen, RCA) for process improvement
Detail‑oriented, proactive, and composed during inspections
Strong interpersonal skills for cross‑functional work
Adaptable and committed to continuous improvement
Benefits
Medical
Prescription
Dental
Vision
Life and disability insurance
Paid time off for vacation, sick and Company recognized holidays
A 401(k) plan
16-week paid parental leave or 26 weeks for the birthing parent
Adoption and fertility support
Tuition reimbursement
Discounts
Company
Reckitt
Reckitt Benckiser Group is a consumer goods company makes health, hygiene and home products.
Funding
Current Stage
Public CompanyTotal Funding
$1.92B2025-09-01Post Ipo Debt· $1.92B
2021-03-01IPO
Leadership Team
Recent News
2026-01-22
2026-01-07
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