Validation Engineer - 167994

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 currently looking for an experienced (CQV) Validation Engineer in Raritan, NJ to work for an innovative and growing pharmaceutical organization. The primary responsibility of this role is to assist with the IQ/OQ/PQ of new instruments/equipment in support of manufacturing operations.

Responsibilities for the (CQV) Validation Engineer include:

• Assist with the development of equipment validation protocols (IQ/OQ/PQ) for new instruments and ensure compliance with applicable regulations and guidelines.
• Conduct equipment validation testing and generate validation reports.
• Provide technical support to manufacturing personnel and troubleshoot any issues related to equipment performance or quality.
• Collaborate with cross-functional teams to ensure timely completion of validation activities.
• Participate in risk assessments and provide recommendations for risk mitigation.
• Assist with the development and implementation of standard operating procedures related to equipment validation and qualification.
• Stay up-to-date with industry trends and regulations related to equipment validation and qualification.

Qualifications for the (CQV) Validation Engineer include:

• Bachelor's degree in Engineering or a related field.
• Minimum of 5+ years of experience in equipment commissioning and validation in a pharmaceutical or medical device manufacturing environment.
• Strong knowledge of applicable regulations and guidelines related to equipment validation (e.g., FDA, EU, ICH).
• Experience with IQ/OQ/PQ protocols, process validation, and risk assessment.
• Excellent problem-solving skills and attention to detail.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a cross-functional team

Compensation for the (CQV) Validation Engineer include:

• Compensation Range is dependent upon experience
• Comprehensive benefits package

Application Period:

This position opens for applications on 6/16/2026 and will remain open for a minimum of 30 days from the posting date.

Keywords

GMP, Pharmaceutical Manufacturing, Equipment Qualification, Equipment Commissioning, Equipment Qualification, IQ/OQ/PQ, Comprehensive Benefits Package, Health, Vision, Dental.