CQV Equipment Validation Engineer — Pharma Manufacturing

Zachary Piper Solutions

Raritan (NJ)

On-site

USD 110,000 - 150,000

Full time

14 days+

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Benefits offered by this job

Comprehensive benefits package

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Job summary

Piper Companies in Raritan, NJ seeks an experienced CQV Commission Qualification Validation Engineer to support IQ/OQ/PQ of new instruments for manufacturing operations.

Requirements include a Bachelor's in Engineering and 5+ years in commissioning/validation in pharma/medical device environments, plus strong FDA/EU/ICH knowledge and IQ/OQ/PQ experience. On-site with comprehensive benefits.

Qualifications

Bachelor's degree in Engineering or related field.
5+ years of equipment commissioning and validation experience in pharma/medical device manufacturing.
Strong knowledge of FDA/EU/ICH guidelines for validation.
Experience with IQ/OQ/PQ protocols and risk assessment.
Excellent problem-solving and communication skills; able to work independently.

Responsibilities

Assist development of IQ/OQ/PQ validation protocols.
Conduct validation testing and generate validation reports.
Provide technical support to manufacturing personnel and troubleshoot equipment issues.
Collaborate with cross-functional teams to meet validation timelines.
Participate in risk assessments and recommendations for mitigation.
Develop and implement SOPs related to equipment validation.
Stay up-to-date with industry trends and regulations.

Skills

Communication

Problem-solving

Independent worker

Cross-functional teamwork

Education

Bachelor's degree in Engineering or related field

Job description

Piper Companies in Raritan, NJ seeks an experienced CQV Commission Qualification Validation Engineer to support IQ/OQ/PQ of new instruments for manufacturing operations.

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