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📑 Job DescriptionWe are currently seeking a talented Remote Veeva Vault Developer with prior experience working in GxP systems. The ideal candidate will possess certifications in the Veeva Vault platform or any one Vault module (RIMS, QDocs, QMS, Promomats, CTMS, eTMF), along with expertise in change management within GxP systems. Additionally, the c ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment • 2 years of experience supporting GxP laboratory applications and systems • Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control • Working knowledge of Active Directory/LDAP and Windows Security • Detail-oriented with problem-solv ...

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📑 **Job Responsibilities:** + Perform review of Computerized System Validation of IT systems of Manufacturing Sites + Support various phases of Computer System including Planning, Implementation, Maintenance and retirement activities by ensuring compliance with internal / external regulatory requirements + Perform ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with problem-solving, ...

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📑 Job Description Participate into SAP Business discussions & technical discussions, execute assigned task in coordination with required stakeholders. Requirement gathering from business in coordination with all stakeholders from manufacturing sites. Analyzing and assessing the requirement received from business. Business requirement document (BRD) p ...

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📑 Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analy ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment • 2 years of experience supporting GxP laboratory applications and systems • Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control • Working knowledge of Active Directory/LDAP and Windows Security • Detail-oriented with problem-solv ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment • 2 years of experience supporting GxP laboratory applications and systems • Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control • Working knowledge of Active Directory/LDAP and Windows Security • Detail-oriented with problem-solv ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment • 2 years of experience supporting GxP laboratory applications and systems • Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control • Working knowledge of Active Directory/LDAP and Windows Security • Detail-oriented with problem-solv ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment • 2 years of experience supporting GxP laboratory applications and systems • Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control • Working knowledge of Active Directory/LDAP and Windows Security • Detail-oriented with problem-solv ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with ...

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📑 Why Patients Need YouEverything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analys ...

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📑 Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis th ...

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📑 Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis th ...

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📑 We're on the hunt for a validation virtuoso with experience of 7+ years to join our client at Noida !Job Description : - If you're passionate about CSV and SDLC concepts like V-Model, Waterfall, and Agile Scrum, we want to hear from you. - But wait, there's more! We need someone who's not just familiar with regulations and guide ...

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📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with problem-solving, ...

🔗 View Salary and More Information 🎯 Get Ai Resume Score for this Job

📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with ...

🔗 View Salary and More Information 🎯 Get Ai Resume Score for this Job

📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with ...

🔗 View Salary and More Information 🎯 Get Ai Resume Score for this Job

📑 • 3 years of hands-on experience maintaining quality control of an I.T. environment• 2 years of experience supporting GxP laboratory applications and systems• Understanding of GAMP 5, 21 CFR Part 11, Computer System Validation, and Change Control• Working knowledge of Active Directory/LDAP and Windows Security• Detail-oriented with ...

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📑 Job Description:Experience: Minimum 10 years of experience in drug product manufacturing / Production of oral dosage form and sterile productsExperience of FDA Approval in the Production/ Manufacturing area (Various Pharmaceuticals Dosage forms) Should be Competent Technical person & Registered PharmacistShould have Production experience, thorough ...

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📑 Why Patients Need YouEverything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis throu ...

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📑 Role - LIMS Developer Experience - 7+ years Location - Bangalore (Preferred) Skills - LIMS , EMPOWERMENT CDS , 21CFR Part 11 and GxP , SOPs Roles and Responsibilities Strong Technical Knowledge on Empower3 FR5 & other CDS Systems Maintaining and supporting current CDS system End user issue support, troubleshooting, & resolution Administrat ...

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📑 Role - LIMS Developer Experience - 7+ years Location - Bangalore (Preferred) Skills - LIMS , EMPOWERMENT CDS , 21CFR Part 11 and GxP , SOPs Roles and Responsibilities Strong Technical Knowledge on Empower3 FR5 & other CDS Systems Maintaining and supporting current CDS system End user issue support, troubleshooting, & resolution Administrat ...

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📑 Role - LIMS Developer Experience - 7+ years Location - Bangalore (Preferred) Skills - LIMS , EMPOWERMENT CDS , 21CFR Part 11 and GxP , SOPs Roles and Responsibilities Strong Technical Knowledge on Empower3 FR5 & other CDS Systems Maintaining and supporting current CDS system End user issue support, troubleshooting, & resolution Administrat ...

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📑 Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desire to create lasting value for clients. Powered by our purpose – the relentless pursuit of a world that works better for peop ...

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📑 Job DescriptionPSC 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 team’s achievements. Employing ...

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📑 Job DescriptionLooking to onboard a seasoned Senior Information Security Project Manager (m/f/d) for a thrilling opportunity with a renowned manufacturing powerhouse nestled in the picturesque surroundings of Bubendorf, BL.ResponsibilitiesManagement of multiple simultaneous projects including their dependencies, creation and delivery of presentatio ...

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📑 Role - LIMS DeveloperExperience - 7+ yearsLocation - Bangalore (Preferred)Skills - LIMS , EMPOWERMENT CDS , 21CFR Part 11 and GxP , SOPsRoles and ResponsibilitiesStrong Technical Knowledge on Empower3 FR5 & other CDS SystemsMaintaining and supporting current CDS systemEnd user issue support, troubleshooting, & resolu ...

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📑 Role - LIMS DeveloperExperience - 7+ yearsLocation - Bangalore (Preferred)Skills - LIMS , EMPOWERMENT CDS , 21CFR Part 11 and GxP , SOPsRoles and ResponsibilitiesStrong Technical Knowledge on Empower3 FR5 & other CDS SystemsMaintaining and supporting current CDS systemEnd user issue support, troubleshooting, & resolu ...

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📑 Release Manager - CREQ186260 Description Release manager JD The role is to meet the IT Service Management requirements for one of the account in HLS domain. The person has to meet the work demand rise in the area of New Business Service Introduction in IT workplace, Change Management and Release management. Tools & Certification ITSM Tools ,Servic ...

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📑 Release Manager - CREQ186260 Description Release manager JDThe role is to meet the IT Service Management requirements for one of the account in HLS domain. The person has to meet the work demand rise in the area of New Business Service Introduction in IT workplace, Change Management and Release management.Tools & CertificationITSM Tools ...

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📑 When our values align, there's no limit to what we can achieve. Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life- changing medicines t ...

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📑 Responsibilities: Responsible for Computer System Validation documents preparation, execution as per the guidelines of IT Manager. Review of QMS & CSV documents of Quality control, R&D, Manufacturing and support Statutory, Customers and EHS Audits. QMS Activities: Responsible for Quality Management System like Deviation log, preparation ...

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📑 Our Team: Main responsibilities: Supporting iEnvision for Managed Access Program (MAP) project lead in implementation and configuration of tool as per the program needs Managing the data flows, data mapping and migrations, and data quality Collaborating closely with country medical teams, global medical teams, vendors, Quality, IT and any ...

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📑 Job Title: Quality Training Lead About Job: Main responsibilities: Manage CHC Global Quality trainings as appropriate: Manage Global CHC GxP Training requirements, curriculum and learner roles for some or all CHC entities with relevant Business Process Owners (BPOs) Provide support to all Local Training administrator for the use of the el ...

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📑 When our values align, there's no limit to what we can achieve. Additional Job Description Home Based, US The Quality Assurance (QA) Compliance Manager has a high level of knowledge and experience of appropriate GxP compliance and other applicable regulations and laws, Parexel procedures and appropriate Parexel processes to conduct audits a ...

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📑 Role - LIMS DeveloperExperience - 7+ yearsLocation - Bangalore (Preferred)Skills - LIMS , EMPOWERMENT CDS , 21CFR Part 11 and GxP , SOPsRoles and ResponsibilitiesStrong Technical Knowledge on Empower3 FR5 & other CDS SystemsMaintaining and supporting current CDS systemEnd user issue support, troubleshooting, & resolution ...

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📑 R&D Project Manager Remote, 6+ month contractThe role of the R&D Project Manager will be to deploy an existing application onto an established platform for an R&D group following the established approach and methodology of previous projects. The R&D project manager's objective is to coordinate the team's efforts and bring the application live by th ...

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📑 R&D Project Manager Remote, 6+ month contractThe role of the R&D Project Manager will be to deploy an existing application onto an established platform for an R&D group following the established approach and methodology of previous projects. The R&D project manager's objective is to coordinate the team's efforts and bring the application live by th ...

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📑 R&D Project Manager Remote, 6+ month contractThe role of the R&D Project Manager will be to deploy an existing application onto an established platform for an R&D group following the established approach and methodology of previous projects. The R&D project manager's objective is to coordinate the team's efforts and bring the application live by th ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include: Responsibilities To maintain consistent ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include: ResponsibilitiesTo maintain consistent and ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include: ResponsibilitiesTo maintain consistent and ...

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📑 Job DescriptionAbout PSC Biotech Who we are? PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management ...

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📑 • Five years of hands-on experience with MES systems • Knowledge of Emerson Syncade • Experience in Computer System Validation (CSV) documentation and a GxP compliant working environment • Experience with global/multi-site manufacturing deployment projects • Experience designing and leading IT business analysis-related workshops Analytical thinkin ...

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📑 • Five years of hands-on experience with MES systems • Knowledge of Emerson Syncade • Experience in Computer System Validation (CSV) documentation and a GxP compliant working environment • Experience with global/multi-site manufacturing deployment projects • Experience designing and leading IT business analysis-related workshops Analytical thinkin ...

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📑 • Five years of hands-on experience with MES systems • Knowledge of Emerson Syncade • Experience in Computer System Validation (CSV) documentation and a GxP compliant working environment • Experience with global/multi-site manufacturing deployment projects • Experience designing and leading IT business analysis-related workshops Analytical thinkin ...

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