kneat jobs

Commissioning & Qualification (CQV) Program Lead

Richmond, Virginia

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Yesterday

Job Title: Commissioning and Qualification Program Lead Work Location: Richmond, VA Type: Long Term Contract Must Haves:15+ years developing and delivering C+Q programs for Greenfield and Brownfield sitesManaging scope, budget, schedule, hiring, performance of C+Q teamsExpertise in GMPs, regulatory frameworks, commissioning, qualification, and ASTM E2500 practices.Handson proficiency with Kneat or similar electronic C&Q/validation platforms.Connecting cross-functionally with different groups (

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Contract, Third Party

Depends on Experience

Commissioning and Qualification (C&Q) Project Manager

Conshohocken, Pennsylvania

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Today

Position: Commissioning and Qualification (C&Q) Project Manager Location: Conshohocken, PA (onsite 2-3 days is mandatory) Position Summary Reporting to the Project CQV Lead, the Commissioning and Qualification (C&Q) Project Manager is responsible for developing and executing the project s C&Q strategy, ensuring delivery within scope, schedule, and budget. This role oversees the C&Q team and all related activities to ensure assets are started up, tested, and qualified for compliant, reliable

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Contract, Third Party

Commissioning and Qualification Program Lead

Virginia Beach, Virginia

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3d ago

Position Tittle: Commissioning and Qualification Program LeadLocation: ONSITE IN VIRGINIAVisa: USCDuration: Long Termplease gothrough the full Jd and send me resumes at or +1 Job Details:15+ years developing and delivering C+Q programs for greenfield sites Managing scope, budget, schedule, hiring, performance of C+Q teams Connecting cross-functionally with different groups (quality, EPCM firms, subcontractors) Coming from pharmaceutical build background Job description Primary ResponsibilitiesP

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Third Party, Contract

100 - 105

CSV Engineer

Pittsburgh, Pennsylvania

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Today

Job Summary: CSV Engineer to support commissioning and validation activities for a newly built Cell & Gene Therapy R&D and manufacturing facility in Pittsburgh, PA. The role focuses on reviewing validation deliverables, ensuring compliance with regulatory standards (21 CFR Part 11, GAMP 5), and coordinating with commissioning teams handling facilities, utilities, MES, EMS, CMMS, and related systems. The consultant will work within environments using Kneat, Microsoft Office, and automation platfo

Full-time

Validation Engineer, Senior

Pennsylvania

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Today

Job Description: We are seeking a highly skilled and experienced Validation Specialist/Engineer to support commissioning and qualification activities for our client's facility in PA. The ideal candidate will have a strong background in executing validation life cycle deliverables in compliance with ISPE C&Q guidelines, with hands-on expertise in analytical instrumentation and controlled temperature unit qualifications. Responsibilities: Develop, review, and execute validation life cycle deliver

Full-time

Validation Engineer, Mid-Level

Marietta, Pennsylvania

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Today

Full-time

Validation Engineer, Senior

Marietta, Pennsylvania

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Today

Full-time

Validation Engineer, Mid-Level

Pennsylvania

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Today

Full-time

W2 Role :- Commissioning and Qualification Program Lead

Richmond, Virginia

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3d ago

Commissioning and Qualification Program Lead Location: Richmond, Virginia (ONSITE) (RELOCATION OPEN) Interview: Virtual Multi-year project MANAGER NOTES: 15+ years developing and delivering C+Q programs for greenfield sites Managing scope, budget, schedule, hiring, and performance of C+Q teams Connecting cross-functionally with different groups (quality, EPCM firms, subcontractors) Coming from a pharmaceutical background Primary Responsibilities Provide strategic leadership for all C&Q activi

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Contract

Depends on Experience

CQV Engineer

Los Angeles, California

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Today

Roles & Responsibilities: Lead qualification of cleanroom facilities and large-scale manufacturing process equipment, including centrifuges and filter presses uthor, execute, and close validation protocols and final reports with minimal oversight Conduct construction walks, pre-check P&IDs, and identify, communicate, and escalate field and design issues Review and approve protocols, SOPs, TOPs, and vendor submittals against specifications and quality standards Drive execution planning, schedulin

Full-time

Commissioning and Qualification Program Lead-Onsite Richmond VA

Hybrid in Richmond, Virginia

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2d ago

Job Title: Commissioning and Qualification Program Lead Location: Onsite Richmond VA Relocation Duration: +12 Months contract Interview: Video 15+ years developing and delivering C+Q programs for greenfield sites Managing scope, budget, schedule, hiring, performance of C+Q teams Connecting cross-functionally with different groups (quality, EPCM firms, subcontractors) Coming from pharmaceutical build background Job description Primary Responsibilities Provide strategic le

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Third Party, Contract

$60 - $70

Validation Engineer

Holly Springs, North Carolina

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Today

Ideal Candidate: 5+ YOE with a B.S. in Science, Engineering, and Pharmacy areas. Standard Hours - hours may vary to support manufacturing (early/later shifts, possible weekends) Cleaning Validation Specialist I Job Description Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Support authoring and executing CV/CHT/SHT protocols, progress package work and wrap up

Full-time

CQV Engineer

Norton, Massachusetts

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Today

Job Summary: The CQV Automation Engineer is responsible for executing and documenting automation commissioning, qualification, and testing activities within a GMP biotech or pharmaceutical manufacturing environment. This role supports automated systems, control equipment, and plant-wide automation networks while ensuring compliance with cGMP, GDP, and regulatory standards. The position requires close collaboration with cross-functional teams and on-site support during commissioning and operation

Full-time

Validation Engineer Senior

Holly Springs, North Carolina

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Today

Fully onsite - 8-5 Monday - Friday - occasional availability needed outside normal hours such as nights or weekends. Ideal candidate: 8+ YOE Must have field execution experience. Lead the execution of all Cleaning Validation activities (CV/SIP PQ/CHT/SHT studies), including protocol generation, field execution, data retrieval/verification, sample management following a Lifecycle Approach and using Kneat. Supports non-traditional work schedule based on project and business needs Leads and pe

Full-time

Validation Engineer Senior

Thousand Oaks, California

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Today

ApTask Global Workforce (AGW) is seeking a Validation Engineer Senior with a biopharmaceutical company. This is a 12+ month contract opportunity with our client located in Thousand Oaks, CA. This is a hybrid position. This position could be extended for up to 3 years. Responsibilities: Lead and/or execute commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities Generate, review, and execute C&Q protocols, plans, and summary re

Full-time

USD 68.17 per hour

Engineering Specialist - Commissioning, Qualification, and Validation (CQV)

Rahway, New Jersey

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Today

Job Description The Engineering Specialist is a key role within Our Company's Research Labs Pharmaceutical Sciences - Pharmaceutical Operations Engineering group (Pharm Ops Engineering), responsible for Commissioning, Qualification, and Validation (CQV) and broader engineering support across non-sterile operations, including formulation, filling, and packaging of Oral Solid Dosage and Inhalation products. The position leads CQV development and execution for new and modified processing equipmen

Full-time

USD 87,300.00 - 137,400.00 per year

Senior Specialist, Automation Engineer (Onsite)

Rahway, New Jersey

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Today

Job Description Job Description: The Formulation, Laboratory, and Experimentation (FLEx) Center in Rahway, New Jersey, includes a cutting-edge drug product cGMP clinical supply manufacturing facility, known as FLEx Non-Sterile. The FLEx facility supports the formulation and filling of clinical, stability, and developmental supplies for Oral Solid Dosage (OSD) and Inhalation products, including critical program needs related to new products undergoing process development, new products undergoing

Full-time

USD 117,000.00 - 184,200.00 per year

Validation Engineer

Boston, Massachusetts

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Today

Job Description: specializing in comprehensive CQV (Commissioning, Qualification, and Validation) and engineering solutions tailored exclusively for the dynamic life science industry. We provide a full spectrum of services, including facilities, utilities, process, and automation engineering, top-tier quality, compliance, and regulatory affairs consulting, and innovative recruiting solutions. Our commitment extends beyond consulting, as we aim to be the next-generation partner providing total ta

Full-time

Engineer - Automation Engineering - Control System Data Analyst- Lilly Medicine Foundry

Lebanon, Indiana

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Today

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Full-time

USD 66,000.00 per year

Sr. Validation Engineer

Wilson, North Carolina

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Today

Summary: The Senior Validation Engineer will lead and execute commissioning and qualification (C&Q) activities for automation systems at the. This role ensures compliance with GMP regulations and internal quality standards, supporting the successful delivery of validation documentation and execution for new and existing systems. Roles & Responsibilities: Lead and manage C&Q lifecycle activities including URS, DQ, IQ, OQ, and PQ for automation and process systems. Collaborate with cross-function

Full-time

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