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- Description Summary: The Clinical Supervisor, in collaboration with and under the direction of the Nursing Department Director/Manager, is accountable for ongoing shift leadership and operations of a clinical department and for nursing care safety and quality. The...SuggestedHourly payFull timeReliefWork at officeShift work
CHRISTUS Health
Placitas, NM1 hour agonew - ...Separation projects Demonstrate strong leadership and stakeholder communication Experience: 7-10+ years of experience in Computer System Validation (CSV) Experience in Pharmaceutical / Biotechnology / Medical Device industry #J-18808-Ljbffr Creative Solutions Services, LLCSuggested
- Roles & Responsibilities: Prior work experience working in pharma or other GMP setting. Strong working knowledge of analytical laboratory IT systems (i.e. Lab Vantage, Empower, Benching, Signals, L7, LabX, MODA, etc.). Solid knowledge of Computer System Validation process...SuggestedWork experience placement
- Roles & Responsibilities: Ex-Pharmaceutical preferred. Experience in the Pharmaceutical, biotechnology, or medical device industry. 2+ years' experience with System Development Lifecyle. 3+ years' experience in Computer System Validation (Based on the role selected)...SuggestedRemote work
- Job Summary 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...Suggested
- Job Summary We 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 & Responsibilities Lead and mature...Suggested
- 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. 7-1...SuggestedRemote work
- IT CSV Analyst needs 5+ years of experience working with Computer System Validations in a GMP pharmaceutical environment. IT CSV Analyst requires: Bachelors degree in Software Engineering, Computer Science, Computer Engineering, or a related field . Minimum of 5+ years...SuggestedLocal area
- ...Electronic Records and Electronic Signature requirements, EU Annex 11, Data Integrity standards, and guidelines. Collaborate closely with CSV Lead, System Integrator, and site team. Prepare and complete all System Design Configuration Specification documentation....Suggested
$95k - $105k
...computerized systems (e.g., System Owner, IT, QA, Departmental Managers, vendors). Provide guidance and support on Computer System Validation (CSV) practices, helping others develop skills and knowledge in regulatory compliance, validation processes, and industry best practices....SuggestedFor contractorsShift work- Job Summary The GxP IT Systems Support / CSV Technical Contractor is responsible for providing hands‑on IT support for computerized systems used in GxP operations. This role focuses on system administration, technical troubleshooting, vendor coordination, maintenance of...SuggestedFor contractors
- Charles River Laboratories in Newark, Delaware, seeks an experienced validator to oversee computerized system validation within CRL Manufacturing Operations. You will manage full lifecycle validation projects, ensuring quality and regulatory compliance. Responsibilities...Suggested
- Responsibilities Responsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all systems are in a qualified state suitable for the intended use. This will include authoring protocols, test scripts, and...SuggestedWork at office
- Corbion in Tucker, Georgia is seeking a CSV IT Engineer to ensure compliance with Good Manufacturing Practices and validate computerized systems in regulated environments. The ideal candidate will support the validation lifecycle across GxP systems and work closely with...Suggested
- Mentor Technical Group (MTG) provides specialized technical support and solutions for FDA-regulated industries. MTG is recognized for its expertise in life sciences engineering, ensuring compliance with pharmaceutical, biotechnology, and medical device safety and efficacy...SuggestedRemote job
$70.49k - $118.06k
...experiences to enhance our collective expertise Senior Validation Engineer Responsibilities: Lead SAP validation strategy and CSA/CSV activities for SAP S/4HANA, ECC, and integrated GxP systems, ensuring compliance with GAMP 5, 21 CFR Part 11, and Annex 11...Temporary workWork experience placementRemote workVerista, Inc.
King of Prussia, PA20 days ago- ...the pharmaceutical and biotech sectors. This role requires hands-on experience with IQ/OQ execution and Computer System Validation (CSV), ensuring strict adherence to compliance and regulatory standards such as 21 CFR Part 11 and GAMP guidelines. The ideal candidate will...
- Creative Solutions Services, LLC is seeking a qualified candidate for a role focusing on validation in the pharmaceutical industry. Candidates should have over 3 years of experience in Computer System Validation and a strong background in FDA regulations. The position requires...
$150k - $200k
Business Development Director, CSV page is loaded## Business Development Director, CSVlocations: Los Angeles, CA: Pasadena, CAtime type: Full timeposted on: Posted Todayjob requisition id: R020595BW Design Group is a fully integrated architecture, engineering, construction...Flexible hours$70.49k - $113.52k
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...Full timeTemporary workWork experience placement- Compunnel, Inc. is seeking a GxP IT Systems Support / CSV Technical Contractor to provide hands-on IT support for their GxP operations. The contractor will be responsible for system administration, technical troubleshooting, and managing configuration specifications. Qualified...For contractors
$76k - $103k
Cipla is seeking a QA Associate (IT) in Hauppauge, NY, to ensure the compliance and performance of IT systems in a pharmaceutical manufacturing environment. You will validate IT systems, focusing on audit trails, data integrity, and GxP compliance. The ideal candidate has...Full time$85k - $122.2k
Dormont Manufacturing Co in Kansas City is seeking a Digital Operations and Application Governance Specialist to execute digital initiatives and ensure application governance. This role offers full-time employment focused on optimizing operations and improving efficiency...Full time- Katalyst CRO is looking for a CSV Consultant in Raritan, NJ to support system validation activities in a regulated environment. The consultant will ensure compliance with FDA guidelines, contribute to validation documentation, and work within the System Development Lifecycle...
- ...automation platforms, collaborating with DTI teams, and ensuring compliance with manufacturing regulations. Ideal candidates will possess relevant degrees and a strong background in quality assurance with experience in CSV and automation support. #J-18808-Ljbffr Planet Pharma
$95k - $105k
Overview: The Computer Systems Validation (CSV) Specialist/Validation Specialist ("CSV Specialist") is an onsite role based at SOFIE's Center of Excellence in Totowa, New Jersey, a 21 CFR 211 and EudraLex Volume 4 compliant manufacturing facility supporting the production...- Creative Solutions Services, LLC is seeking a CSV Analyst with expertise in Instrument Integration & Validation to ensure compliance and validation in regulated environments. The role involves validating laboratory and manufacturing software systems, developing protocols...
- Lilly seeks a Lab CSV and Compliance Analyst to validate and maintain computerized lab systems at the LP1 Lebanon, IN site. You will ensure DI/CSV standards across systems like MODA, LabVantage, Empower, and NuGenesis, while coordinating with CSQA and Quality teams. You...
- ...a vital role in executing digital initiatives and maintaining robust application governance within the plant. You will support project delivery, ensure CSV compliance, and drive adoption of digital solutions for operational efficiency. #J-18808-Ljbffr Procter & GambleWorldwide
- ...Development and Project Management teams to deliver quality solutions. The ideal candidate will have at least a year of experience in CSV for clinical trials, technical writing skills, and a keen attention to detail. Join Veeva to help speed up therapy delivery. #J-1880...Remote job
