CQV Engineer: Pharmaceutical Equipment Validation

Piper Companies; Raritan (NJ); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies is seeking an experienced CQV Commission Qualification Validation Engineer in Raritan, NJ to support IQ/OQ/PQ of new instruments and equipment for manufacturing operations. You will develop validation protocols, conduct testing, generate reports, and collaborate with cross-functional teams to ensure timely validation activities.

A Bachelor's degree in Engineering and 5+ years in pharmaceutical equipment validation are required, with strong regulatory knowledge and problem-solving

Qualifications

• 5+ years of experience in equipment commissioning and validation in pharma/medical device manufacturing.
• Bachelor's degree in Engineering or related field required.
• Knowledge of FDA/EU/ICH regulations related to equipment validation.
• Experience with IQ/OQ/PQ protocols, process validation, and risk assessment.
• Strong problem-solving and attention to detail.
• Excellent communication and interpersonal skills.
• Ability to work independently and in cross-functional teams.

Responsibilities

• Assist with development of equipment validation protocols (IQ/OQ/PQ).
• Conduct validation testing and generate validation reports.
• Provide technical support to manufacturing personnel and troubleshoot equipment issues.
• Collaborate with cross-functional teams to ensure timely validation activities.
• Participate in risk assessments and mitigation recommendations.
• Assist with SOP development and implementation for equipment validation.

Skills

5+ yrs exp

CQV validation

Problem solving

Communication

Independence

Cross-functional

Education

Bachelor's degree in Engineering

Tools

IQ/OQ/PQ protocols

Process validation

Regulatory guidelines

Job description

Piper Companies is seeking an experienced CQV Commission Qualification Validation Engineer in Raritan, NJ to support IQ/OQ/PQ of new instruments and equipment for manufacturing operations. You will develop validation protocols, conduct testing, generate reports, and collaborate with cross-functional teams to ensure timely validation activities.

A Bachelor's degree in Engineering and 5+ years in pharmaceutical equipment validation are required, with strong regulatory knowledge and problem-solving