Average salary: $114,500 /yearly
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...environmental impact.This role will work as a member of the Automation Engineering Department at Eli Lilly, Foundry. The engineer will provide... ...site and/or for capital projects. This role will provide CSV support leading and executing CSV activities for process automation...SuggestedFull timeWork experience placementH1bLocal areaVisa sponsorshipWork visaFlexible hours$115k - $126.5k
Job Title: Automation CSV EngineerLocation: Redmond, WADepartment: Global MSATAbout Us: this is who we areAt Evotec, we believe that... ...you!The Role: / your challenge, …in our journeyThe Automation CSV Engineer is responsible for supporting validation, compliance, testing,...SuggestedFull timeTemporary workFlexible hours- ...Job Responsibilities: ~Review and approve CSV lifecycle documents (VMP, URS, FRS, HDS, Risk Assessments, IQ/OQ/PQ, RTM, Summary Reports). ~Ensure risk-based validation approaches aligned with GAMP 5, 21 CFR Part 11, and Data Integrity (ALCOA+) principles. ~Evaluate...Suggested
SGS Consulting
Florida, FLmore than 2 months ago - ...Manufacturing your Cell Therapies from Benchtop to Bedside.Job SummaryCellipont Bioservices is growing, and we are looking for a Lead CSV Engineer who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and...Suggested
Cellipont Bioservices
Spring, Montgomery County, TX25 days ago - ...Industrial Automation/CSV Engineers VTI Life Sciences (VTI) is seeking forward-thinking, ambitious engineers looking to accelerate their careers in the pharmaceutical, biotechnology, and medical device industries. We offer an opportunity to support our teams of industry...SuggestedContract workTemporary workRelocation
VTI Life Sciences
United Statesmore than 2 months ago - ...Job Description Job Description LOCATION: Manatí, Puerto Rico We are seeking a CSV / Automation Engineer to support pharmaceutical projects in Manatí, Puerto Rico. The engineer will support Computerized System Validation (CSV), automation, commissioning, qualification...SuggestedContract workPart timeWork at office
LEGAL PROJECT MANAGEMENT PARTNERS LLC
Puerto Rico4 days ago - ...validation documentation including but not limited to: User Requirements Specifications (URS) Design Reviews (DR) Criticality assessments CSV protocols (SAT, IQ, OQ, PQ) which verify if the system is compliant to regulatory and client requirements Reports which summarize the...Suggested
- ...Independently support Business Separation activities for Large global & regional GxP Computerized systems. With minimal supervison. Strong CSV Expertise, especially within Acquisition/Divestiture/Separation. Ability to manage end-end from Inventory, assessments, remediations...SuggestedRemote work
- Job-ID32980009Reference26-01707Summary: We are currently looking for an experienced CSV (Computer System Validation) Engineer to join our team in Plymouth, MN.Roles & Responsibilities: Develop and execute Computer System Validation (CSV) strategies, plans, protocols, and...Suggested
- ...Position Summary We are seeking an experienced Senior Computer System Validation (CSV) Engineer to support validation activities for GMP-regulated manufacturing and automation systems at client. The ideal candidate will have extensive experience validating computerized...SuggestedShift work
Inteldot
Texasa month ago - Bristol Myers Squibb in Devens, MA is seeking a Senior Engineer for Lab Automation who will manage lab automation software and qualified... ...have 5+ years in pharma lab operations and strong knowledge of CSV, GMP, FDA guidelines, and cyber security. This role offers comprehensive...Suggested
- ...looking for a qualified candidate for a role focused on Technology Quality Manufacturing and MES Services. This position requires a strong CSV and Quality expertise for leading validation activities across the SDLC in GxP systems with a desire for 7-10 years of relevant...SuggestedRemote work
- Job-ID32337885Reference26-00750 Job Summary: Seeking a Sr. CSV Engineer with 10+ years of experience in pharmaceutical compliance, Computerized System Validation (CSV), and GxP-regulated environments. The ideal candidate should have expertise in compliance regulations...SuggestedLocal area
- Job-ID32840712Reference26-01429 Job Description: The Senior Computer System Validation (CSV) Engineer is responsible for leading validation activities for computerized systems used in regulated environments such as pharmaceutical, biotechnology, or medical device manufacturing...Suggested
- Creative Solutions Services, LLC is seeking an experienced Computer System Validation (CSV) Consultant to support a biotech client in validating bioinformatics software and data analysis platforms within a GMP-regulated environment in Norwood, MA. Responsibilities include...Suggested
- ...Job Description Job Description This is a remote position. CSV Quality Engineer Lead- Part-Time Location: Remote Commitment: Approximately 20 hours per week Role type: Part-time The Opportunity A growing technology company serving pharmaceutical...Part timeRemote work
Genovice
Atlanta, GA21 days ago - ...To support a strategic software integration program, the full-time Senior CSV Engineer will provide quality and validation expertise throughout the lifecycle of computerized systems in a remote role, ensuring compliance with GxP requirements and data integrity principles...Full timeRemote work
Virtual Vocations Inc
United States1 day ago - Job-ID32293289Reference26-00631 Job Summary: Shop Floor CSV/CSA Lead/Engineer responsible for leading and executing validation deliverables across the lifecycle in regulated manufacturing and laboratory GMP/GLP environments. The role includes automation/controls validation...
- Job-ID32873467Reference26-01480Job 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...
- Job-ID32367022Reference26-00831 Job Summary: The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role directly supports gene therapy...
- Job-ID26109845Reference24-00076A global pharmaceutical company is rapidly developing facilities and needs CSV Engineers to support projects starting in February 2024. The CSV Engineers will need to have experience supporting automated manufacturing lines and processes for...
- ...Assist site Automation groups in configuring I/O and executing CSV protocol requirements. Independently perform CSV lifecycle deliverables... ...Report Requirements: Bachelor's degree in Computer Science, Engineering, or a related field. Minimum of 2-5 years of experience in...Work experience placementRemote work
- Job-ID32187977Reference26-00480 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...
- Job-ID32263931Reference26-00597 Roles & Responsibilities Lead end-to-end CSV activities (inventory assessment remediation disposition) Support business separation for large GxP systems Define & implement risk-based validation strategies Review & approve test plans, UAT...Remote work
- ...About The Role We are looking for a Senior CSV Engineer to lead validation projects for our top-tier pharma clients. You will be responsible for defining validation strategies, executing protocols, and ensuring compliance with 21 CFR Part 11. Key Responsibilities Develop...
Weltraw Consulting Group
New York, NY3 days ago - Pharmaron is seeking a Software Validation Senior Associate in Exton, PA to lead CSV efforts for GxP laboratory software and systems. You will develop validation plans, risk assessments, and regulatory documentation, collaborating with Quality, IT and system owners to ensure...
- Job-ID32288194Reference26-00624 Job Summary:The CSV Engineer / Validation Engineer will be responsible for ensuring computerized systems in a regulated pharmaceutical environment comply with GxP, 21 CFR Part 11, GAMP 5, EU Annex 11, ISO 9001, and SOX requirements. The...
- Job-ID32301345Reference26-00641Summary:Our client is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate must have hands-on experience with...
- Job-ID32200742Reference26-00496Summary: IT CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. This role will focus on validating ERP Master Data Governance processes...
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides... ...Summary We are seeking a Computer System Validation (CSV) Specialist/Engineer to support validation activities for computerized...
Validation & Engineering Group, Inc
Wilson, NC17 days ago
