OQ jobs

Rensselaer, New York

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Today

Summary: We are seeking a Commissioning Engineer to join one of our largest pharmaceutical clients 5x/week onsite in Rensselaer, NY. This individual will be joining the engineering team within the Engineering and Automation space assisting in the commissioning of their stainless-steel pressure vessels in a new facility. Roles & Responsibilities: They will be responsible for assisting in the full life cycle starting with detail design through commissioning, FAT/SAT, IQ/OQ/PQ and qualifications.

Full-time

Validation Lead with Oracle Process Manufacturing -(Healthcare domain)

Chicago, Illinois

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Yesterday

Role :- Validation Lead with Oracle Process Manufacturing (OPM)Location :- Chicago, IL-OnsiteDuration :- 12+ Months Role Overview:We are seeking a skilled Validation Testing Specialist with deep expertise in Oracle Process Manufacturing (OPM) to support validation efforts across manufacturing systems.The ideal candidate will ensure compliance with regulatory standards and deliver high-quality validation documentation and testing outcomes. Key Responsibilities:Lead validation testing activities f

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Third Party, Contract

Depends on Experience

CQV Engineer

Boston, Massachusetts

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Today

Responsibilities: Generate, execute, review, finalize, and approve validation/qualification protocols and reports. Manage and update project validation plans for specific projects. ssist and deliver amendments to the qualification(s) to ensure qualification compliance within agreed upon timelines. Utilize computerized asset management system for managing validation/qualification schedules. Generate operational and maintenance SOPs, FATs, URSs, FRSs, validation protocols and reports. Requirements

Full-time

Mid-Sr. Process Development Engineer

Maple Grove, Minnesota

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28d ago

Job Title: Mid-Sr. Process Development Engineer Job Location: Maple Grove, MN Project Duration: 12 Months- Contract to Hire Pay Rate: $45/hr - $63/hr (depending on experience) Job Description: Daily Responsibilities: -Owning equipment, processes, inspections, development builds, and driving improvements in the associated technology and methodology -Positioning future projects for success to continue driving Human Visual Inspection (HVI) reduction for Watchman manufacturing automation + validatio

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Contract

$45 - $63

Principal Engineer

New Albany, Ohio

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Today

Payrate: $48.00 - $50.20/hr. Summary: The Principle Engineer will work closely with team members to develop detailed engineering specifications, device design & development, support verification, validation, and regulatory submissions of these devices. The role of the Principle Engineer is to work within a cross-functional organization to utilize technologies and methodologies that support short-cycle robust device development. Responsibilities: Work cross-functionally with individuals and proj

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Contract

$48 - $50.2 hr

Validation Engineer

Birmingham, Alabama

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Today

Responsibilities: Develop URS, SIC and SRA for new and existing aseptic facilities and equipment. Develop and execute Commissioning (COM) and Installation qualification (IQ) protocols to ensure that systems are installed correctly and according to specifications. Perform operational qualification (OQ) and performance qualification (PQ) activities to verify that systems operate as intended under all conditions. Ensure all documentation is compliant with regulatory requirements and internal qualit

Full-time

Validation Engineer II - Logan, UT

Logan, Utah

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Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing so

Full-time

Sr. CSV Engineer

Oregon City, California

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Today

Summary : Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies. Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment and control systems Create and modify validation documentation including but

Full-time

CSV Engineer

Bothell, Washington

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Today

Summary: Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies. Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment and control systems Create and modify validation documentation including but

Full-time

GMP & GxP Business Analyst

Remote

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18d ago

GMP & GxP Business AnalystLocation: RemoteDuration: Long Term Roles & ResponsibilitiesGather, analyze, and document business and user requirements across functional teams.Act as the primary liaison between Business, IT, end users, and cross-functional stakeholders during project execution and maintenance phases.Analyze business challenges and support evaluation of appropriate IT solutions.Collaborate with managers and end users to ensure alignment and buy-in for proposed solutions.Develop detail

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Contract

Depends on Experience

Lead Validation Engineer

Wilson, North Carolina

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Today

Summary: The Lead Validation Engineer will oversee and drive commissioning and qualification (C&Q) activities for automation and process systems at a regulated manufacturing site. This leadership role is responsible for ensuring validation strategies align with regulatory expectations and project goals, while mentoring a team of validation professionals and coordinating with cross-functional stakeholders. Roles & Responsibilities: Lead the planning, execution, and documentation of C&Q lifecycl

Full-time

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

CSV Engineer

San Francisco, California

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Today

Summary: We are looking for a skilled CSV Engineer with strong experience in Veeva systems to support validation, compliance, and implementation activities in a regulated life sciences environment. The ideal candidate will have hands-on experience working on Veeva platforms and ensuring systems meet GxP and 21 CFR Part 11 compliance. Roles & Responsibilities : Perform Computer System Validation (CSV) activities for Veeva applications. Develop and execute validation documents: URS, FRS, IQ, OQ,

Full-time

Field Operator I/II/III

Carlsbad, New Mexico

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Today

An exciting career awaits you At MPC, we?re committed to being a great place to work ? one that welcomes new ideas, encourages diverse perspectives, develops our people, and fosters a collaborative team environment. POSITION SUMMARY: This position is responsible for monitoring and maintaining all equipment associated with and not limited to remote compressor stations, valve sites and pipelines. This position is responsible for the daily operational duties associated with and not limited to th

Full-time

Field Operator

Bloomfield, New Mexico

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Today

Full-time

New Product Introduction (NPI) Process Engineer

Santa Clarita, California

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Today

Responsibilities: Manage prototype and pilot builds for new product introduction, including operator training and coordination with production planning. Collaborate cross-functionally with Manufacturing and Quality teams to ensure process adoption and compliance. pply Design for Manufacturability (DFM) principles to tooling, process design, and product integration. Support the R&D team with Design Verification (DV) testing and technical reporting. Plan and execute Process Validations (IQ/OQ/PQ)

Full-time

Validation Engineer

Austin, Texas

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Today

Summary: We are seeking a talented Validation Engineer to join our team. As a Validation Engineer, you will play a crucial role in ensuring the quality and compliance of our manufacturing processes and systems. You will be responsible for designing, implementing, and executing validation protocols to ensure that equipment, facilities, and processes meet regulatory requirements and industry standards. Roles & Responsibilities: Design and develop validation protocols for SCADA technology used in t

Full-time

Staff Engineer, Equipment Engineering

Salt Lake City, Utah

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Today

Work Flexibility: Onsite What You'll Do Lead the launch of new equipment: oversee Factory Acceptance Testing (FAT), safety checks, and setup to ensure smooth integration into production.Enable success on the floor: train and mentor operators, technicians, and maintenance teams in equipment use and best practices.Champion safety & compliance: ensure all equipment meets safety standards, conduct risk assessments, and engage with regulatory officials as needed.Optimize performance: develop prevent

Full-time

Senior Validation Engineer

Warsaw, Indiana

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Today

Roles & Responsibilities: Develops and Executes Process Validation Strategies Creates plans, protocols (IQ, OQ, PQ), and risk assessments to ensure effective processes for medical devices and equipment. Ensures Regulatory Compliance Adheres to FDA (21 CFR 820), ISO 13485, and other relevant regulations, participating in audits and maintaining up-to-date knowledge. nalyses Data and Reports Findings Compiles and analyzes validation data, writes comprehensive reports, and identifies trends for proc

Full-time

AWS Infrastructure Qualification & Validation Specialist

Redwood City, California

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Today

Summary: We are seeking a skilled professional to lead and execute Infrastructure Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documentation for AWS-hosted environments. This role is critical in ensuring our cloud infrastructure meets regulatory compliance standards (e.g., GxP, HIPAA, ISO 27001) through robust validation and documentation practices. Roles & Responsibilities: Develop and maintain IQ/OQ/PQ documentation for AWS infrastructure components. C

Full-time

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