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- Job-ID33106038Reference26-01817 Summary: 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...Suggested
- ..., and GAMP methodologies. * Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment... ...(URS) Design Reviews (DR) Criticality assessments CSV protocols (SAT, IQ, OQ, PQ) which verify if the system is compliant...Suggested
- ...quality, cloud concepts, cloud applications, etc. In addition to validation and regulation experience, the resource should have the... ...regional GxP Computerized systems. With minimal supervison. Strong CSV Expertise, especially within Acquisition/Divestiture/Separation...SuggestedRemote work
- Job-ID32311628Reference26-00679Summary: Provide validation and testing services to ensure system integrity, data accuracy, and regulatory... ...compliance of migrated records Compliance & Data Integrity Support CSV (Computer System Validation) activities and documentation...Suggested
- Job Title: CSV Consultant (Computer Systems Validation) Location: Redwood City, CA Type: Contract Job Summary We are seeking an experienced CSV Consultant to support validation activities across multiple GxP-regulated systems within a pharmaceutical environment. This...SuggestedContract work
- STAAR Surgical in Lake Forest is seeking a Director of Software Validation to lead software validation efforts across various platforms. The role involves managing teams, ensuring compliance with FDA regulations, and improving validation practices. Candidates should have...Suggested
- Pharmaron Beijing Co. Ltd. is seeking a Software Validation Senior Associate in Exton, PA to lead CSV efforts for laboratory software and systems. You will design validation strategies, plans, and documentation, coordinating with IT, Quality, and system owners to ensure...Suggested
- Job DescriptionConsultant - SAP S/4HANA Validation Lead (Life Sciences)We are looking for people who have demonstrated proven success in... ...SAP implementation program.Key Responsibilities1. Own and drive CSV activities for SAP ECC to SAP S/4HANA transformation programs and...SuggestedFull timeTemporary work
- ...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 experience. Key...SuggestedRemote work
- ...Job Description Job Description This is a remote position. SR CSV Validation Engineer Location: Remote Role type: Contract The Opportunity A growing technology company serving pharmaceutical and other regulated manufacturing environments is...SuggestedContract workRemote work
$115k - $140k
...The incumbent is responsible for leading computerized systems validation projects and supporting the data integrity program. This includes... ...appropriately documented Support quality events involving CSV in protocol nonconformances, deviations, investigations, CAPAs,...SuggestedContract workLive inWork at officeVisa sponsorship- Job DescriptionPrincipal– SAP Computerized System Validation (CSV), Life Sciences- Business ConsultingWe are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation for ERP applications like ECC/SAP S/4 HANA...SuggestedFull timeTemporary workLocal area
- ...members that embody these values. Job Description Summary Krystal Biotech is seeking a highly motivated Computer System Validation (CSV) Associate to support validation and compliance activities for GxP computerized systems used in Manufacturing, Quality Control...SuggestedFull time
- ...8Reference26-00595 Roles & Responsibilities: Manage end-to-end validation lifecycle (Inventory, Assessment, Remediation, Final Disposition... ...7-10+ years of experience in Computer System Validation (CSV) Experience in Pharmaceutical / Biotechnology / Medical Device...Suggested
- Job-ID32308611Reference26-00654Job Description: We are seeking an experienced CSV Lead to support the validation of computer systems for a newly constructed Sterile Drug Product Clinical Manufacturing Facility. This role will play a key part in supporting the transition...SuggestedFlexible hours
- 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-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-ID32345409Reference26-00769 Job Description: 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...
- ...offer a competitive compensation package and professional development. Summary The CSV Specialist is responsible for planning, executing, and documenting computer system validation activities for GxP-regulated computerized systems within a pharmaceutical...Work at officeLocal area
- Job-ID32952841Reference26-01653 Summary: We're looking for an experienced Computer System Validation (CSV) Consultant to support a leading biotech client in validating bioinformatics software, scientific algorithms, and data analysis platforms within a GMP-regulated environment...
- ...pharmaceutical company is rapidly developing facilities and needs CSV Engineers to support projects starting in February 2024. The... ...processes for pharmaceutical products and should have experience validating automated systems. The CSV Engineer will also have...
- 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...
- Job-ID32217193Reference26-00544Job Summary: Responsible for leading and maturing the Validation / Computer System Validation (CSV) program, ensuring compliance with GxP and FDA requirements. The role focuses on driving validation strategy, closing compliance gaps, supporting...
- ...93173Reference26-00628 Summary : We are seeking an experienced Validation Engineer to support pharmaceutical manufacturing and quality operations... ...in IQ/OQ/PQ, process validation, cleaning validation, CSV, and equipment qualification. Knowledge of FDA regulations, cGMP...
- ...Reference26-00489 Job Summary: We are seeking a detail-oriented Validation Engineer to support validation and calibration activities for... ...in equipment qualification and computerized system validation (CSV). Roles & Responsibilities: Perform validation and calibration...
- ...Reference26-00442 Roles & Responsibilities: We are seeking a seasoned Validation Engineer with 10+ years of experience in medical device or... ...Method Validation (TMV) and Computerized System Validation (CSV) in accordance with GAMP 5. A solid working knowledge of...
- ...quality and Perform GxP and 21 CFR part 11 assessments and develop a validation plan. Develop functional risk strategy and perform functional... ...(oral and written) and attention to detail. Experience in CSV/Validation in Pharmaceuticals or Medical Device domain with experience...
- ...enhancing their technical capabilities and increasing productivity.Additional requirement:"Strong expertise in Computer System Validation (CSV) processes and methodologies, ensuring compliance with regulatory standards such as FDA 21 CFR Part 11, GxP, and healthcare-specific...
- ...ID29052371Reference24-01969 Responsible for managing end-to-end CSV deliverables for both new & existing applications. Responsible... ...Assessment, Traceability Matrix, protocols (IQ, OQ, PQ), Interim Memo & Validation Summary Report QA Review of the following CSV Deliverables:...For contractorsInterim role
- ...by filling resource gaps, ensuring projects remain on track during critical milestones. Document and support Computer Systems Validation (CSV) tasks as needed to meet regulatory requirements. Requirements: Bachelor's degree in Engineering, Science, or related field. Experience...