Cqv Validation Engineer - 5,958+ job offers

Title: CQV Validation Engineer ( GMP / Kaye Systems ) Location: Greater Boston Area, MA (Hybrid 2–3 days onsite) Employment Type: Contract Status: Accepting Candidates About the role Join a high-impact engineering team supporting commissioning, qualification, and validation activities within a regul

Lead CQV Engineer / Lead Validation Engineer on-site, full-time in Devens, MA. J.D: Lead Validation Engineer Responsibilities: Lead second shift CQV execution activities across multiple systems and workstreams Coordinate daily execution priorities to recover schedule slippage and maintain timelines

Stellent IT LLC

Lead CQV Engineer / Lead Validation Engineer on-site, full-time in Devens, MA. J.D: Lead Validation Engineer Responsibilities: Lead second shift CQV execution activities across multiple systems and workstreams Coordinate daily execution priorities to recover schedule slippage and maintain timelines

Stellent IT LLC

Senior CQV Engineer / Senior Validation Engineer Devens, Massachusetts 3 months contract- 6/15-9/15 Senior Validation Engineer Responsibilities: Execute IQ/OQ protocols and support operational verification activities Perform Drawing walkdowns (P&IDs, system verification) Perform Equipment/component

Description Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve s

Description Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve s

We are seeking a CQV Engineer to support commissioning, qualification, and validation activities within a pharmaceutical manufacturing environment. The ideal candidate will have experience supporting sterile and non-sterile equipment qualification projects and working closely with vendors and cross-

Role:CQV Engineer Location: USA(Multiple) Job Overview We are seeking a CQV Engineer to support commissioning, qualification, and validation activities for equipment, utilities, and facilities within a GMP-regulated pharmaceutical environment. This is an entry-level role ideal for recent graduates o

Job Title: CQV Engineer Locations: Mesa, AZ Duration: 6+ Months Role Overview We are seeking experienced CQV Engineers to support qualification and validation activities for sterile and non-sterile manufacturing systems within pharmaceutical operations. This role will focus on equipment qualificatio

Job Summary We are seeking a motivated and detail-oriented Validation / CQV Engineer to support qualification and validation activities in a regulated pharmaceutical/biotech environment. The ideal candidate will have hands-on experience in IQ/OQ execution, Computer System Validation (CSV), and valid

Title: CQV Engineer – Downstream Biologics Validation Location: Devens, MA Employment type : (W2/1099) Job Summary We are hiring CQV Engineers to support a fast-paced biologics expansion project within a large-scale cell culture manufacturing facility. This role is heavily focused on hands-on qualif

Title: CQV Engineer (Second Shift) Location: Devens, MA Duration: 03-04+ months Pay rate: $40/hr -$45/hr on W2 Role: CQV resources supporting an NPD large-cap project modifying existing equipment and processes for future methods in an existing large-scale cell culture facility Focus on process equip

This is a 7+ mos. contract. Project Start Date: May 18, 2026 Project End Date: December 31, 2026 Resource Location: New Albany, OH (100% onsite) Duration: 40 hours per week until EOY, possible extension Scope: CQV Engineer Sterile & non-sterile experience Temp Mapping Autoclaves Freezers Washers

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 protocolsideal for professionals who thrive on the manufacturing floor. Roles & Responsibili

Job Title: CQV Automation Engineer Locations: Ohio (OH) / New Jersey (NJ) Experience: 1–2 Years Employment Type: W2 Job Description: We are seeking a Junior CQV Automation Engineer with experience in commissioning, qualification, validation (CQV), and automation systems to support pharmaceutical or

Role Summary We are looking for CQV Engineers / System Owners to take ownership of specific process and utility systems within either the Bulk (Drug Substance) or Fill Finish (Drug Product) areas on a large-scale greenfield project. This role focuses on system ownership across the full CQV lifecycle

Position Summary We are seeking a CQV Lead with hands-on experience in Oral Solid Dose (OSD) manufacturing who brings both strong engineering fundamentals and a modern, digital-first approach to validation delivery. This role is intended for engineers who own qualification outcomes end-to-end—from i

QvalFocus Inc.

Role Summary Looking for a Validation Specialist with 1–3 years of CQV experience and hands-on exposure to Kneat Gx. This role is heavily focused on validation documentation, with most of the work involving writing and executing protocols. Key Responsibilities Execute IQ, OQ, PQ, and requalification

Job Title: CQV Engineer - Pharma Location: Devens, MA Duration: 6 - 12 Months Position Overview: Our client is seeking CQV Engineers to support an NPD large-cap project involving modification of existing equipment and processes for future methods within an existing large-scale cell culture facility.

Intellectt Inc

Job Title: CQV Engineer (Commissioning, Qualification & Validation) Location: Lehigh Valley, Pennsylvania (Onsite) Employment Type: Contract Duration: 12–24 Months Job Summary We are seeking an experienced CQV Engineer to support commissioning, qualification, and validation activities within an asep