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Lead solution design leveraging DG tools, such as Informatica IDMC, Collibra, Alation, or open source and cloud-native capabilities (AWS, Azure, GCP)Troubleshoot and Resolve technical issuesCoach junior team members and lead DG technical competencies and skills strengthBusiness DevelopmentNeed to actively contribute to Pre-Sales / Business Development of the Data Governance domain.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Familiar with the development of CSV documentation (Validation Plans, Requirements, Design / Configuration Specifications, Test Scripts [IQ/OQ/PQ/UAT], Summary Reports, Trace Matrices, SOPs.
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR part 11 electronic records and electronic signatures, and good documentation practices with the ALCOA+ principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles.
$59 - $61 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing.
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A Specialist Senior at Deloitte works within an engagement team and is responsible for prototyping, process design (including scenario design, flow mapping), testing, training, development in APEX, DevOps. integrations, data migration, deployments, Visualforce, and lightning Aura.
$131,175 - $218,625 a yearFull-timeExpandApply NowActive JobUpdated 6+ months ago - UpvoteDownvoteShare Job
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Coordinates the efforts of Clinical Trial Supplies Packaging with Clinical Supplies Manufacturing, Clinical Research, Pharmaceutical Development, Quality Assurance, and Regulatory Affairs with the objective of establishing a plan to have clinical supplies available within the agreed time frame.
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The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES team to create, manage, and improve computerized systems/Recipes validation deliverables for electronic systems, applications, and associated controls to maintain data integrity supporting ALCOA+ principles throughout the CSV lifecycle.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Specialist will be responsible for ensuring the validation of the S12 Enterprise Manufacturing Execution System (EMES), and applications are done following the relevant Client procedures, such as CSV SOP but no limited and applicable health authority regulations.
ExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Minimum of 2+ years relevant work experience required preferably in a pharmaceutical manufacturing environment. Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe Authoring/Validation.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Ability to work extended hours or a modified work schedule to assist manufacturing operations support model, including 12x7 on-call support rotation. Operate effectively and with minimal supervision, within a team or independently, performing projects and related duties.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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An equivalent combination of education, experience and training may substitute. Understanding the concept of Critical thinking for Computerized Systems. With advanced technical document writing and time management skills, including ability to prioritize and manage expectations.
ExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Job Title: Qlik and Google Sheets Dashboard Integration Specialist. Job Description : We seek a skilled specialist in Qlik and Google Sheets to integrate dashboards with clients' KPI, ensuring automated updates and data accuracy.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. - Understanding of the drug development process.
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Net, Angular, SQL, and SQL Server, with a strong understanding of Agile development practices. Provide input and support for component and data architecture design, technology planning, and testing.
$53.93 - $59.06 an hourExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Participate in full systems life cycle management activities, including analysis, design, coding, testing, and implementation of web applications. Familiarity with Agile development, story/task estimation, and GIT source control.
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