Piper Companies
Piper Companies
is currently seeking an experienced
Validation Engineer (CSV/CQV)
in
New Jersey
to work for an industry leading Pharmaceutical company. Responsibilities For The Validation Engineer (CSV/CQV) Provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance with GMP and FDA standards. Conduct IQ, OQ, and PQ activities, as well as validate new laboratory equipment and methods. Support software updates and assist in creating SOPs, safety protocols, and work instructions. Oversee site validation master plans, ensure equipment and systems meet regulatory requirements, and drive continuous improvement initiatives. Collaborate with internal teams and external partners to communicate project progress effectively. Qualifications For The Validation Engineer (CSV/CQV) Bachelor’s degree in Chemical Engineering, Biomedical Engineering, or a related field. Over 3 years of experience in biotechnology and/or pharmaceutical industries. Proficient in drafting SOPs, validation reports, and work instructions. Skilled in reviewing and approving validation protocols and reports for facility/equipment commissioning, qualification, and change management. Compensation For The Validation Engineer (CSV/CQV) Pay Range: $60-$65/HR Long Term Contract Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays This job opens for applications on 10/3/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords:
Validation, CSV, CQV, IQ, OQ, PQ, technical writing, Biomedical Engineering, Pharmaceutical, Biotechnology, Laboratory Equipment, Manufacturing Equipment, Equipment Validation, Equipment Commissioning, Validation Maintenance, Cleaning Validation
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is currently seeking an experienced
Validation Engineer (CSV/CQV)
in
New Jersey
to work for an industry leading Pharmaceutical company. Responsibilities For The Validation Engineer (CSV/CQV) Provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance with GMP and FDA standards. Conduct IQ, OQ, and PQ activities, as well as validate new laboratory equipment and methods. Support software updates and assist in creating SOPs, safety protocols, and work instructions. Oversee site validation master plans, ensure equipment and systems meet regulatory requirements, and drive continuous improvement initiatives. Collaborate with internal teams and external partners to communicate project progress effectively. Qualifications For The Validation Engineer (CSV/CQV) Bachelor’s degree in Chemical Engineering, Biomedical Engineering, or a related field. Over 3 years of experience in biotechnology and/or pharmaceutical industries. Proficient in drafting SOPs, validation reports, and work instructions. Skilled in reviewing and approving validation protocols and reports for facility/equipment commissioning, qualification, and change management. Compensation For The Validation Engineer (CSV/CQV) Pay Range: $60-$65/HR Long Term Contract Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays This job opens for applications on 10/3/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords:
Validation, CSV, CQV, IQ, OQ, PQ, technical writing, Biomedical Engineering, Pharmaceutical, Biotechnology, Laboratory Equipment, Manufacturing Equipment, Equipment Validation, Equipment Commissioning, Validation Maintenance, Cleaning Validation
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