Pharma CQV Validation Engineer (IQ/OQ/PQ)

Piper Companies; Raritan (NJ); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies is seeking an experienced CQV Validation Engineer in Raritan, NJ, to assist with the IQ/OQ/PQ of new instruments/equipment. This role involves developing validation protocols, conducting testing, and providing technical support to ensure compliance with regulations.

The ideal candidate should have a Bachelor's degree in Engineering and a minimum of 5 years of experience in pharmaceutical validation environments. Strong knowledge of FDA regulations and excellent problem-solving skills are essential.

Qualifications

• Minimum of 5+ years of experience in pharmaceutical equipment validation.
• Strong knowledge of regulations related to equipment validation.
• Experience with IQ/OQ/PQ protocols and risk assessments.

Responsibilities

• Assist with the development of equipment validation protocols.
• Conduct equipment validation testing and generate reports.
• Provide technical support and troubleshoot equipment issues.

Skills

Equipment commissioning and validation

Knowledge of FDA regulations

Problem-solving skills

Communication skills

Education

Bachelor's degree in Engineering or related field

Job description

Piper Companies is seeking an experienced CQV Validation Engineer in Raritan, NJ, to assist with the IQ/OQ/PQ of new instruments/equipment. This role involves developing validation protocols, conducting testing, and providing technical support to ensure compliance with regulations.

The ideal candidate should have a Bachelor's degree in Engineering and a minimum of 5 years of experience in pharmaceutical validation environments. Strong knowledge of FDA regulations and excellent problem-solving skills are essential.