fme Life Sciences focuses on Business Solution technology implementations that leverage Content Services platforms for clients in the Life Sciences Industry.
The company is recognized as a trusted vendor and partner by clients ranging from small start-ups to large global pharmaceutical companies.
The Senior Technical Lead will oversee and drive data and document migration projects, along with enterprise content management (ECM) implementations.
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.
The position requires a Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or a related field.
A minimum of 8 years of experience in data and document migration, ECM implementation, or related fields is required, with at least 3 years in a leadership role within the life sciences industry.
The role is remote but may require occasional travel to project sites or client meetings.
Requirements:
A Bachelor’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 essential.
Advanced experience in ECM platforms (e.g., Veeva Vault, OpenText Documentum, Generis CARA), data and document migration tools, SQL, XML, and scripting languages is required.
A strong understanding of life sciences regulations and compliance requirements, including experience with validation processes and GxP-validated systems, is necessary.
Proven leadership abilities and a track record of managing complex projects are required.
Strong problem-solving, prioritization, and communication skills are essential, 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 preferred.
The candidate must be self-driven, flexible, and able to work in a fast-paced environment.
Benefits:
Medical, Dental & Vision plans are provided.
A 401k plan with company match is available.
Life Insurance and Short & Long-term Disability Plans are included.
Paid Time Off (Vacation, Sick/Personal & Paid Holidays) is offered.
An Employee Referral Program is in place.
Opportunities for Training & Development and participation in Company Retreats are provided.
Wellness Resources and an Employee Assistance Program are available for employees.