Validation Engineer

Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Copiague, NY.

Responsibilities for the Validation Engineer

• Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.
• Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.
• Coordinate validation efforts across shifts, providing technical guidance and resolving product or equipment issues.
• Support regulatory inspections and maintain communication with departments and the Corporate Validation Manager.
• Participate in projects and perform additional duties as assigned.

Qualifications for the Validation Engineer

• Bachelor's in Chemical/Biological Sciences or Engineering and 3+ years in liquid pharmaceutical roles required.
• Strong expertise in FDA process validation guidelines, validation methodology, and related technical disciplines (QC, QA, Engineering, Regulatory).
• Proficient in technical writing, Office 365, and statistical tools, with Oracle and QMS experience preferred.
• Skilled in time management, multitasking, and collaboration across cross-functional teams at all levels.
• Cleaning Validation Experience a plus
• Flexible to work off-shifts, weekends, holidays, and travel for validation support.

Compensation for the Validation Engineer

• Salary Range: $100,000-105,000
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 4/23/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Copiague, NY.

Responsibilities for the Validation Engineer

• Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.
• Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.
• Coordinate validation efforts across shifts, providing technical guidance and resolving product or equipment issues.
• Support regulatory inspections and maintain communication with departments and the Corporate Validation Manager.
• Participate in projects and perform additional duties as assigned.

Qualifications for the Validation Engineer

• Bachelor's in Chemical/Biological Sciences or Engineering and 3+ years in liquid pharmaceutical roles required.
• Strong expertise in FDA process validation guidelines, validation methodology, and related technical disciplines (QC, QA, Engineering, Regulatory).
• Proficient in technical writing, Office 365, and statistical tools, with Oracle and QMS experience preferred.
• Skilled in time management, multitasking, and collaboration across cross-functional teams at all levels.
• Cleaning Validation Experience a plus
• Flexible to work off-shifts, weekends, holidays, and travel for validation support.

Compensation for the Validation Engineer

• Salary Range: $100,000-105,000
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 4/23/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.