csv

CSV/DeltaV EngineerLocation: Worcester, MAPlease note: We are only considering W2 candidates at this time. Applications from third-party vendors or C2C arrangements will not be considered.ADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Head-quartered near San Francisco,...

Job Title- CSV AnalystJob Location - WestPoint, PA (Hybrid, must visit site 3 days a week)Job Description-• Lead CSV compliance activities for capital and strategic projects.Must have worked in CSV in Manufacturing automation systems like DELTA V,PI Historian, PLC, LAB Automation Systems(any one pf the systems or all).• Develop, Review and approve...

This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area. This role will be supporting validation leads to help ensure the required deliverables and testing are complete according to the Client CSV SOP. Effective communication is key...

South Chicago, United States | Posted on 09/30/2026 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our...

Job-ID32892427Reference26-01520 Job Description: We are seeking an experienced Computer System Validation (CSV) Lead to oversee validation activities for computerized systems used in regulated GxP environments. The ideal candidate will have extensive experience in CSV lifecycle management, FDA and global regulatory compliance, validation documentation, risk...

Request for Technology Quality Manufacturing and MES Services - 100% allocation / North America (Onshore). Must have: Strong CSV and Quality expertise with ability to independently lead validation activities across the SDLC for GxP systems with minimal supervision. 7-10 years of relevant experience. Proven experience with Manufacturing, MES, and Data...

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.CSV SpecialistProfessional Aguadilla, PR, PR3 days ago Requisition ID: 1067About the Role:As a CSV Specialist within the Professional, Scientific, and Technical Services industry, you will play a critical...

This position requires the following requirements for employment at Stallergenes Greer and includes but is not limited to:Execute pharmaceutical CSV validation project assignments including implementation of new systems, remediation of legacy, and re-validation of existing computerized systemsEvaluate, and define technical needs and make...

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.CSV SpecialistProfessional Aguadilla, PR, PR2 days ago Requisition ID: 1067About the Role:As a CSV Specialist within the Professional, Scientific, and Technical Services industry, you will play a critical...

Job-ID Reference Job Summary: We are looking for a Computer System Validation (CSV) Engineer to support our client in Newark, DE. In this role, you will be responsible for ensuring that computerised systems used in regulated environments are validated and compliant with industry standards. You will work closely with IT, Quality, and business teams...

Description The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of complex computerized systems, custom-developed applications, enterprise databases, data platforms, and business intelligence solutions used within regulated GxP environments. This role partners with IT, Software Development, Data Engineering,...

Job Title: CSV Validation Consultant - Pharma Location: Plainfield,NJ (Hybrid) Experience: 10 years Job Description Experience in Computer System Validation (CSV) within the Pharmaceutical/Life Sciences industry. Strong knowledge of GxP, FDA 21 CFR Part 11, GAMP 5, and data integrity requirements. Experience preparing/reviewing URS, FRS, Risk...

CSV Tester – MES Release SupportProject: MES Release Support – Separation ProjectStart Date: ImmediateIndustry: Pharmaceutical / Life Sciences experience will be a plus Position OverviewWe are looking for experienced Computer System Validation (CSV) Testers to support the release of a Manufacturing Execution System (MES) as part of a separation...

Job Title- CSV Lead Job Location- Raritan, NJ (onsite)   Job Description- • Candidates need to have hands-on experience in validating and implementing infrastructure systems associated with Infrastructure related applications. • Experience in the Pharmaceutical, biotechnology, or medical device industry • 2+ years’ experience with System...

Job SummaryWe are seeking a Lead CSV / Validation Consultant (Director-Level) for a biotech client with an upcoming FDA inspection. This is a critical position focused on program maturity, SaaS validation, and audit readiness.Roles & ResponsibilitiesLead and mature the Validation / CSV programAssess gaps and drive remediation roadmapPrepare for FDA audit and...

We are seeking a CSV Analyst with Instrument Integration & Validation expertise to support validation and compliance of laboratory, manufacturing, and embedded software systems in regulated environments.The role focuses on the integration layer, ensuring data moves accurately and completely from instruments through Instrument Manager into the LIS and related...

Job Description: Seeking experienced CSV Engineers to provide onsite validation support within a regulated biopharmaceutical manufacturing environment. The primary focus of the position will be Computer System Validation, while also supporting equipment qualification and broader CQV activities as project priorities require. Consultants will support...

4 Computer System Validation (CSV) Engineers to lead 4 teams of CSV Specialists Locals required for hybrid-onsite (1st week will be onsite for onboarding, training, etc.) Location: Houston, TX - Hybrid / On-Site as Required Duration: 36 months+ Experience Required: Minimum 10 Years Target Skills: Kneat validation software, DeltaV Distributed Control...

Responsible for supporting equipment and process validation activities within a regulated environment, ensuring compliance with GMP, FDA, and Food/Consumer industry standards.The role focuses on validation lifecycle execution, risk-based approaches, and cross-functional collaboration to maintain product quality and regulatory compliance.Develop, execute, and...

Overview The Infosys Healthcare unit is dedicated to transforming the healthcare industry by leveraging cutting-edge AI-driven solutions to simplify complexities and enhance patient experiences. We focus on creating connected ecosystems, optimizing operations, and delivering superior care across all touchpoints. Join us to be a part of a team that is at the...