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Senior Technical Lead - Veeva Quality - Remote

Posted 3 weeks ago
Software Development
Full Time
USA

Overview

fme Global Life Sciences specializes in delivering comprehensive business solutions with a focus on data and document migration, enterprise content management (ECM) system implementation, and business consulting services. We serve a diverse client base in the Life Sciences industry, ranging from innovative start-ups to large global pharmaceutical companies. As a recognized leader, we provide expert consulting, tailored data and document migration, and ongoing support to meet critical needs in Regulatory Information Management (RIM), Clinical, and Quality Management System (QMS) domains. Our strategic partnerships with leading ECM vendors like Veeva Vault, OpenText Documentum, Generis CARA, Ephesoft, and Alfresco enable us to offer unparalleled expertise and service to our clients.

In Short

  • Oversee data and document migration and implementation projects for Veeva Quality.
  • Serve as the subject matter expert managing all technical aspects of the project.
  • Collaborate with Project Managers and engage with stakeholders to ensure project success.
  • Lead a global team of technical consultants, fostering a collaborative work environment.
  • Provide technical guidance covering architecture, design decisions, and best practices.
  • Identify and mitigate technical risks and challenges during project execution.
  • Ensure adherence to quality assurance practices and support QA teams.
  • Stay updated with industry trends and promote continuous improvement.
  • Support pre-sales activities by providing technical expertise and tailored solutions.
  • Engage in thought leadership through knowledge sharing and industry insights.

Requirements

  • In-depth technical expertise with Veeva Quality and the Life Sciences industry.
  • Strong leadership abilities and experience managing technical teams.
  • Excellent verbal and written communication skills.
  • Ability to collaborate with both business and IT teams.
  • Strong understanding of pharmaceutical validation and relevant regulations.
  • Experience in project management and stakeholder engagement.
  • Ability to identify and manage risks effectively.
  • Commitment to continuous learning and professional development.
  • Experience in pre-sales support and client interactions.
  • Creative problem-solving skills and a results-oriented mindset.

Benefits

  • Opportunity to work with leading ECM vendors and technologies.
  • Collaborative and supportive work culture.
  • Engagement with a diverse client base in the Life Sciences sector.
  • Professional development and continuous learning opportunities.
  • Competitive compensation and benefits package.
fme US logo

fme US

fme US, LLC, operating under fme Life Sciences, specializes in Business Solution technology implementations tailored for the Life Sciences Industry. The company is recognized as a trusted partner for a diverse clientele, ranging from emerging startups to large global pharmaceutical firms. fme excels in business consulting, systems integration, and ongoing support services, particularly in Content Services, which includes Document Management. Their expertise encompasses critical business solutions such as Regulatory Information Management (RIM), Clinical, and Quality Management Systems (QMS). With partnerships with leading vendors like Veeva and OpenText, fme prioritizes client satisfaction by delivering effective technology deployments and comprehensive managed services, setting them apart in the competitive landscape.

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