CQV Validation Engineer (IQ/OQ/PQ) - Pharma Manufacturing

ZP Group; Raritan (NJ); On-site; USD 110,000 - 140,000; Full time

Job summary

Piper Companies is seeking an experienced CQV Validation Engineer in Raritan, NJ to support IQ/OQ/PQ activities for new instruments and equipment in manufacturing operations.

The role requires a Bachelor's in Engineering and 5+ years in pharmaceutical equipment commissioning/validation, with strong regulatory knowledge (FDA, EU, ICH), problem-solving, and cross-functional collaboration.

Qualifications

• Bachelor's degree in Engineering or related field.
• 5+ years in equipment commissioning and validation in pharma/med device.
• Knowledge of FDA, EU, ICH guidelines related to validation.
• Experience with IQ/OQ/PQ protocols and risk assessment.
• Strong problem-solving and attention to detail.
• Strong communication and interpersonal skills.

Responsibilities

• Assist with development of IQ/OQ/PQ protocols for new instruments.
• Conduct equipment validation testing and generate validation reports.
• Provide technical support to manufacturing personnel and troubleshoot issues.
• Collaborate with cross-functional teams to complete validation activities.
• Participate in risk assessments and provide mitigation recommendations.
• Assist with SOP development and implementation for equipment validation.
• Stay up-to-date with industry trends and regulations related to validation.

Skills

IQ/OQ/PQ protocols

Equipment validation

Regulatory compliance

Cross-functional collaboration

Problem-solving

Communication skills

Education

Bachelor's degree in Engineering

Job description

Piper Companies is seeking an experienced CQV Validation Engineer in Raritan, NJ to support IQ/OQ/PQ activities for new instruments and equipment in manufacturing operations.

The role requires a Bachelor's in Engineering and 5+ years in pharmaceutical equipment commissioning/validation, with strong regulatory knowledge (FDA, EU, ICH), problem-solving, and cross-functional collaboration.