Remote Senior Technical Lead - Veeva Quality

Description:

• fme Global Life Sciences specializes in delivering comprehensive business solutions focused on data and document migration, enterprise content management (ECM) system implementation, and business consulting services.
• The company serves a diverse client base in the Life Sciences industry, including innovative start-ups and large global pharmaceutical companies.
• fme provides expert consulting, tailored data and document migration, and ongoing support in Regulatory Information Management (RIM), Clinical, and Quality Management System (QMS) domains.
• The company has strategic partnerships with leading ECM vendors like Veeva Vault, OpenText Documentum, Generis CARA, Ephesoft, and Alfresco.
• The Senior Technical Lead will oversee and drive data and document migration and implementation projects for Veeva Quality for enterprise clients.
• This role requires deep technical expertise, strong leadership abilities, and a thorough understanding of the life sciences landscape.
• The Senior Technical Lead will serve as the subject matter expert, managing all technical aspects of the project and leading the technical team.
• Close collaboration with the Project Manager and engagement with internal and external stakeholders is essential for project success.
• Responsibilities include project planning, communication and collaboration, team leadership, technical guidance, stakeholder management, risk management, change management, quality assurance, continuous improvement, thought leadership, and pre-sales support.

Requirements:

• A Bachelor’s or Master’s degree in Computer Science, Information Technology, Life Sciences, or a related field is required.
• A minimum of 8 years of experience in data and document migration, ECM implementation, or related fields is necessary, with at least 3 years in a leadership role within the life sciences industry.
• Extensive experience in architecting, installing, designing, implementing, configuring, and troubleshooting ECM systems and applications is required.
• Advanced experience in Veeva Vault Quality (QMS and QualityDocs), data and document migration tools, SQL, XML, and scripting languages is essential.
• A strong understanding of life sciences regulations and compliance requirements, including experience with validation processes and GxP-validated systems, is necessary.
• Proven leadership abilities with a track record of managing complex projects and excellent problem-solving skills are required.
• Strong critical thinking, analytical, problem-solving, and conflict-resolution skills, along with a client-focused approach, are essential.
• Strong verbal and written communication skills are necessary, with the ability to convey technical concepts to non-technical stakeholders.
• Experience working with clients across international markets and managing globally distributed technical project teams is required.
• Candidates must be authorized to work in and live in the US, preferably on the east coast due to client scheduling.

Benefits:

• The position offers Medical, Dental & Vision plans.
• A 401k plan with company match is provided.
• Life Insurance and Short & Long-term Disability Plans are included.
• Paid Time Off (Vacation, Sick/Personal & 10 Paid Holidays) is offered.
• An Employee Referral Program is available.
• Opportunities for Training & Development and Company Retreats are provided.
• Wellness Resources and an Employee Assistance Program are included.