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Sr DeltaV Automation Engineer

Intone Networks Inc.

•

Michigan, USA

Full-time, Third Party, Contract

Sr DeltaV Automation Engineer - Muskegon, MI - onsite Job Summary: This is an onsite role to help with commissioning efforts of a DeltaV system and mentor other Junior and Intermediate Engineers. The client and the project team have been working very well together with high collaboration, communication, adaptability, and a good sense of camaraderie making the work environment enjoyable and engaging. We're looking someone who is strong technically but also a great team player, collaborative, an
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Posted 27 days ago | Updated moments ago

Manufacturing Technician (2nd shift)

Cube Hub, Inc.

•

Redwood City, California, USA

Contract

Job Title : Manufacturing Technician Location : Redwood City, CA, 94063 Duration : 12 months Contract-possible to extend Shift Details : 2nd shift-1:30 Pm to 10PM Pay Range : $23/hr. - $25/hr. Job Description: Typical Accountabilities o Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role. Complete all required training on the Code of Conduct and supporting Policies and Stand
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Posted 4 days ago | Updated 7 hours ago

CSV Lead

Laiba Technologies LLC

•

Raritan, New Jersey, USA

Third Party, Contract

Role: CSV Lead Location - Raritan, NJ(Hybrid) 7-10 years experience in Computer System Validation of EMS and BMS applications Must have experience in Agile methodology and handled multiple releases in parallel Extensive knowledge in CSV, CSV auditing, creation and revision of CSV documentation, experience with EMS/BMS, project management, test script review, test execution review, test defect management. Has working experience in any one or two of the following domains Tool validation like Serv
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Posted 1 hour ago

CSV Lead - Raritan, NJ

Shrive Technologies LLC

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New Jersey, USA

Contract, Third Party

Job Details: 7-10 years' experience in Computer System Validation of EMS and BMS applications Must have experience in Agile methodology and handled multiple releases in parallel Extensive knowledge in CSV, CSV auditing, creation and revision of CSV documentation, experience with EMS/BMS, project management, test script review, test execution review, test defect management. Has working experience in any one or two of the following domains Tool validation like ServiceNOW, Automation tools, JIRA Gu
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Posted 18 hours ago | Updated 18 hours ago

Senior Pharma GxP Project Manager with a strong background in SAP S/4 HANA validation

Pioneer Corporate Services Inc

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Foster City, California, USA

Contract, Third Party

Job Title: Senior Pharma GxP Project ManagerLocation: Hybrid Foster City, CA (Locals or nearby states preferred)Duration: 12 Months Job Description:We are seeking a Senior GxP Project Manager with a strong background in SAP S/4 HANA validation and Life Sciences industries. The role demands excellent stakeholder and change management skills, hands-on validation expertise, and solid project leadership. Must-Have Skills: 15 20 years of overall experience 8+ years in Computer System Validation (CSV)
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Posted 20 hours ago | Updated 1 hour ago

CSV Engineer

Katalyst Healthcares and Lifesciences

•

Raritan, New Jersey, USA

Full-time

Roles & Responsibilities: 7-10 years' experience in Computer System Validation of SAAS systems, and Cloud systems. Must have experience in Agile methodology and handled multiple releases in parallel. Has working experience in any one or two of the following domains Tool validation like Service NOW, Automation tools, JIRA. Guide the project team with the right set of applicable project deliverables based on project type and category while catering to the SDLC. Application of FDA guidance's a
Posted 8 days ago | Updated 5 hours ago

SAP Finance FICO Consultant

URSI Technologies Inc.

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Remote

Contract

SAP Finance FICO Consultant San Francisco, CA Remote Remote Qualifications The ideal candidate will have hands-on experience in SAP S4HANA and ECC, a strong understanding of GAMP 5, cGMP, and SOX compliance requirements, and proven application support skillsKey Responsibilities: Provide application support for SAP FICO modules within a regulated IT environmentTranslate business requirements into SAP solutions using SAP Best Practices, FIORI apps, and embedded analyticsJob description : 9+ to 15
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Posted 7 days ago | Updated 23 hours ago

System Validation Engineer

Katalyst Healthcares and Lifesciences

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Santa Clara, California, USA

Full-time

Responsibilities: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software. Support audits and inspections by regulatory bodies, ensuring that non-product software systems comply with quality and documentation standards. Ensure computerized systems are appropriately validated Assessment of applicabi
Posted 5 days ago | Updated 5 hours ago

Medical Device Engineer

Katalyst Healthcares and Lifesciences

•

North Chicago, Illinois, USA

Full-time

Responsibilities: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software. Support audits and inspections by regulatory bodies, ensuring that non-product software systems comply with quality and documentation standards. Ensure computerized systems are appropriately validated Assessment of applicabi
Posted 6 days ago | Updated 5 hours ago

Validation Engineer

Source Code Technologies LLC

•

Sunnyvale, California, USA

Contract

Role name: Validation Engineer Branch | City | Location: Sunnyvale/ Santa Clara, CA Duration: 6 Months Keywords: Key Words to search in Resume Computer System Validation, 21 CFR Part 11, GxP, FDA, 21 CFR Part 11, ISO 13485, IEC 62304 Role Description: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development.Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product sof
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Posted 7 days ago

Medical Device & Regulations Engineer

Katalyst Healthcares and Lifesciences

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Santa Clara, California, USA

Full-time

Responsibilities: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software. Support audits and inspections by regulatory bodies, ensuring that non-product software systems comply with quality and documentation standards. Ensure computerized systems are appropriately validated Assessment of applicabil
Posted 10 days ago | Updated 5 hours ago

Reliability Engineer

Cushman & Wakefield

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Boston, Massachusetts, USA

Full-time

Job Title Reliability Engineer Job Description Summary This individual will provide support for GxP Facility Operations/Engineering department at Vertex GxP sites as part of the Reliability Engineering team. The ideal candidate will be responsible for ensuring the reliability and performance of our equipment/systems through Reliability best practices and continuous improvement initiatives. This role will also execute documentation/forms/spreadsheets to roll out Maintenance and Reliability Best
Posted 9 days ago | Updated 5 hours ago

Control Engineer with Strong Exp. Programming Rockwell/Allen-Bradley PLCs

Combined Computer Resources

•

Pensacola, Florida, USA

Contract

Job Summary: We are seeking a skilled Control Engineer with hands-on experience in programming Rockwell PLCs and designing robust safety circuits. The ideal candidate will work closely with Mechanical Engineers and Technicians to modify, enhance, and commission control systems in a regulated environment. Key Responsibilities: Design, program, and debug Rockwell/Allen-Bradley PLC systems.Evaluate and implement machine safety circuits (ISO 13849, IEC 62061 compliance).Collaborate with Mechanical E
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Posted 21 days ago

SUD Validation Engineer

Thermo Fisher Scientific

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Logan, Utah, USA

Full-time

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
Posted 22 days ago | Updated 5 hours ago

CSV Engineer

Katalyst Healthcares and Lifesciences

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Portsmouth, New Hampshire, USA

Full-time

Responsibilities: Hands on experience in Implementation & Validation of various computerized systems like MES (Syncade) & PLC (COTS). Strong knowledge of Software Development Lifecycle (SDLC), including 21CFR part 11/Annex 11, Data Integrity and computerized system validation requirements. Experience at working independently as well as in a team-oriented, collaborative environment is essential. Author and Execute CSV life cycle documentation. Requirements: CSV experience of 4+ years.
Posted 60+ days ago | Updated 5 hours ago

Sr DeltaV Automation Engineer

TeamSuccess LLC DBA HiEd Success

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Muskegon, Michigan, USA

Contract

Sr DeltaV Automation Engineer Muskegon, MI - onsite Please note: We need someone who has developed automation code within DeltaV (Control Modules through to Equipment Modules, Phases and Recipes) and familiar with troubleshooting code errors, not just associates with a background in using DeltaV from on operator perspective. Job Summary: This is an onsite role to help with commissioning efforts of a DeltaV system and mentor other Junior and Intermediate Engineers. The client and the project tea
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Posted 36 days ago | Updated 28 days ago

Validation Lead

TechDigital Corporation

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King of Prussia, Pennsylvania, USA

Third Party, Contract

Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management 10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP applications and is able to perform document/process Compliance Analysis Adept with Agile and Waterf
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Posted 20 days ago

CSV Automation Engineer(Onsite) Location: North Kansas City, KS (Onsite)

Stellent IT LLC

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Kansas City, Kansas, USA

Third Party, Contract

Title - CSV Automation Engineer (Onsite) Location: North Kansas City, KS (Onsite) Duration: 3-6 Months (most likely 6) Industry: Pharmaceutical Job Description: We are currently seeking a highly experienced Computer System Validation (CSV) Automation Engineer to join an active pharmaceutical project in North Kansas City, KS. The engineer will play a key role in ensuring validated automation systems meet both regulatory and technical standards in a dynamic and fast-paced environment. The ideal
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Posted 8 days ago | Updated moments ago

Computer System Validation (CSV) Engineer

Katalyst Healthcares and Lifesciences

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Remote or Massachusetts, USA

Full-time

Responsibilities: Lead and execute CSV activities across GxP-regulated systems (LIMS, MES, ERP, etc. Author and maintain validation deliverables: URS, FS, DS, IQ, OQ, PQ, and traceability matrices. Ensure systems comply with 21 CFR Part 11, EU Annex 11, and GAMP 5. Support system implementations, upgrades, and periodic reviews. Collaborate with QA, IT, and business users to drive validation strategy. Participate in audits and inspections to demonstrate compliance. Requirements: Bachelor's
Posted 13 days ago | Updated 5 hours ago

DC Technician -- 3841 S. Ellsworth Road, Mesa, AZ 85212 - W2 Role

Sureminds Solutions

•

Mesa, Arizona, USA

Full-time

Physical layer: fiber optic connections, contamination, cleaning Understand ESD best practices Comfortable with text based CLI Familiar with IP based networking A+/Network+ level of knowledge required Good understanding of OSI layer and network principles 2+ years of DC experience required 4+ years of IT related experience required Familiarity with the Linux based systems and experience with scripting and automation (Bash, Python, Perl) Understanding BGP routing protocols, spanning tree
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Posted 17 hours ago