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Remote or Hybrid in Indianapolis, Indiana

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8d ago

Job Title: Senior CQV Engineer/Manager Location: Remote / Hybrid / Onsite (Depending on Project Requirements) Duration: Long-Term Contract Position Overview We are seeking an experienced CQV (Commissioning, Qualification & Validation) professional to support and lead validation activities within highly regulated pharmaceutical, biotechnology, and life sciences environments. This role will be responsible for ensuring GMP compliance across facilities, utilities, equipment, manufacturing processes,

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Contract

Depends on Experience

CQV Engineer

Massachusetts

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Today

Summary : We are looking for hands-on CQV Engineers to support a high-impact biologics project within a GMP-regulated environment. This is a fast-paced opportunity focused purely on execution of validation protocols-ideal for professionals who thrive on the manufacturing floor. Roles & Responsibilities: Execute IQ/OQ protocols for process equipment Perform equipment walkdowns and verify against design Support SIP/CIP cycles, wet testing, and temperature mapping Work with downstream equipment (ch

Full-time

Senior CQV Engineer/Senior Validation Engineer Consultant

Massachusetts

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Today

Job Summary: Senior CQV Engineer / Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ protocols, equipment verification, temperature mapping, SIP/CIP validation activities, deviation support, and ensuring compliance with GMP/GDP standards while collaborating with Engineering, QA, and Operations teams. Roles & Responsibilities: Execute Installation Qualif

Full-time

CQV Engineer

Remote or Raritan, New Jersey

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Today

Summary: This position will be responsible for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be responsible in handling day-to-day activities inclusive of execution, protocol management, vendor management, issues, deviations, corrections and remediation efforts for facility, equipment, systems and processes in support of personalized cell therapy production through safe and compliant manufa

Full-time

Validation Engineer/Technician with CSV / CQV Focus

Worcester, Massachusetts

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9d ago

Arthur Lawrence is looking for a Validation Engineer/Technician with CSV / CQV Focus one of our clients in Worcester, MA. Please find the job description below and send us your updated resume if interested: Must-Have Skills: Experience in validation, calibration, or CQV within a pharmaceutical or regulated environment Strong knowledge of GMP and 21 CFR Part 11 compliance, including CSV (Computerized System Validation) Hands-on experience with equipment qualification (IQ/OQ/PQ), process validati

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Contract

$40+

Pharma CQV Lead

Harvard, Massachusetts

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Yesterday

We are seeking a Lead CQV Engineer / CQV Project Manager to serve as the primary CQV technical lead for project scope. This resource will own CQV execution strategy, deliverable approach, reviewer alignment, documentation quality, deviation strategy, and technical oversight across equipment workstreams. Lead CQV Engineer Responsibilities: Lead CQV strategy and execution planning for GMP equipment qualification scope Own documentation strategy for URS revisions, readiness checklists, IOQ/PQ proto

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Contract

45 - 55

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