Validation Engineer - 167994

Piper Companies

Raritan (NJ)

Presencial

USD 110.000 - 140.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Comprehensive benefits package

Descripción de la vacante

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

The ideal candidate has a bachelor's degree in engineering and 5+ years in pharma equipment validation, with strong knowledge of FDA/EU/ICH guidelines and excellent problem-solving and communication skills. This is an onsite role offering a comprehensive benefits package.

Formación

  • Bachelor's degree in Engineering or a related field required.
  • Minimum 5+ years of equipment commissioning and validation experience in pharma/medical device manufacturing.
  • Strong knowledge of FDA, EU, ICH regulations related to equipment validation.
  • Experience with IQ/OQ/PQ protocols, process validation and risk assessment.
  • Excellent problem solving and attention to detail; strong communication skills.

Responsabilidades

  • Assist with development of IQ/OQ/PQ validation protocols for new instruments.
  • Conduct validation testing and generate validation reports.
  • Provide technical support to manufacturing and troubleshoot equipment issues.
  • Collaborate with cross-functional teams to complete validation activities on time.
  • Participate in risk assessments and recommend mitigation strategies.
  • Assist with SOP development related to equipment validation and qualification.
  • Stay updated on industry trends and regulations for validation.

Conocimientos

Problem-solving
Communication
Independent work
Cross-functional collaboration

Educación

Bachelor's degree in Engineering or related field

Herramientas

IQ/OQ/PQ protocols
Process validation
Risk assessment

Descripción del empleo

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.

#LI-KT1 #LI-ONSITE

Consigue la evaluación confidencial y gratuita de tu currículum.

o arrastra y suelta tu archivo aquí

Similar jobs

Puestos de trabajo similares que vale la pena comparar

CQV Validation Engineer — Lead IQ/OQ/PQ for Equipment
CQV Validation Engineer — Lead IQ/OQ/PQ for Equipment

Piper Companies • Raritan (NJ)

Presencial
USD 110.000 - 140.000
Comprehensive benefits package
Commission Qualification Validation Engineer
Commission Qualification Validation Engineer

Piper Companies • Titusville (NJ)

Presencial
USD 100.000 - 150.000
Health, Vision, Dental insurance
Comprehensive benefits package
CQV Specialist
CQV Specialist

Piper Companies • Titusville (NJ)

Presencial
USD 83.000 - 96.000
Medical benefits
Dental benefits
Vision benefits
+1
CQV Engineer
CQV Engineer

Piper Companies • Titusville (NJ)

Presencial
USD 83.000 - 90.000
Validation Engineer – Pharmaceutical & Medical Device (CQV, CSV, IQ/OQ/PQ)
Validation Engineer – Pharmaceutical & Medical Device (CQV, CSV, IQ/OQ/PQ)

Stark Pharma Solutions Inc • West Chicago (IL)

Presencial
USD 90.000 - 130.000
CQV Engineer: Pharma Equipment Validation & Compliance
CQV Engineer: Pharma Equipment Validation & Compliance

Piper Companies • Titusville (NJ)

Presencial
USD 100.000 - 150.000
Health, Vision, Dental insurance
Comprehensive benefits package
CQV Engineer
CQV Engineer

Trinity Consultants Engineering & EHS Workforce Solutions • El Segundo (CA)

Presencial
USD 120.000 - 160.000
Validation Engineer
Validation Engineer

Inteletech Global Inc • Jersey City (NJ)

Presencial
USD 55.104
CQV Validation Engineer
CQV Validation Engineer

Shoolin Inc • North Carolina

Presencial
USD 75.000 - 100.000
CQV Engineer
CQV Engineer

Stark Pharma • Philadelphia

Presencial
USD 90.000 - 130.000