Analytical Validation Engineer

Piper Companies is seeking an Analytical Validation Engineer to join a major pharmaceutical manufacturing company located in Titusville, NJ. This role is 100% onsite. The Analytical Validation Engineer will ensure the accuracy and reliability of processes, equipment, and systems in pharmaceutical manufacturing by conducting thorough validation, commissioning, and decommissioning activities to maintain compliance and operational excellence. 

Responsibilities of the Analytical Validation Engineer include:  

• Oversee end-to-end validation for products, processes, equipment, and packaging, including managing IQ, OQ, and PQ for manufacturing equipment to ensure the highest standards. 
• Provide expert decisions on validation strategies and address performance issues to maintain optimal operations. 
• Prepare, review, and organize detailed validation protocols and reports, ensuring thorough and accurate documentation. 
• Schedule and oversee validation tasks across all shifts, ensuring seamless operations and continuous improvement. 
• Support inspections and ensure compliance with Good Manufacturing Practices (GMP), maintaining the highest quality standards. 

Qualifications for the  Analytical Validation Engineer include:  

• Minimum of 5 years' experience in a GMP environment. 
• Independently manage multiple projects and tasks, driving efficiency and ensuring timely completion of critical initiatives. 
• Utilize exceptional interpersonal skills, including flexibility, collaboration, and inclusivity, to foster a cohesive and dynamic team environment. 
• Leverage your self-starter attitude to develop innovative solutions, overcoming challenges and enhancing operational effectiveness. 
• Apply sharp analytical aptitude and critical thinking skills to key concepts, driving success and ensuring high-quality outcomes. 
• Bachelor’s Degree in Chemistry, Biology, or Biochemistry 

Compensation for the  Analytical Validation Engineer include:  

• Salary Range: $55-$60 hr.  
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law, and Holidays  

This job opens for applications on 3/21/2025. Applications for this job will be accepted for at least 30 days from the posting date.  

Keywords: Validation Engineer, Analytical Validation, Process Validation ,Equipment Validation, GMP Compliance, IQ, OQ, PQ, FDA Regulations, Pharmaceutical Manufacturing, Liquid Formulations, Technical Writing, Statistical Analysis, Quality Assurance, Validation Protocols, Validation Reports, Process Improvement, Risk Assessment, Regulatory Compliance, Quality Management Systems (QMS), Data Analysis, Project Management 

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