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Technical Project Manager - Life Sciences Domain

VUEVERSE CONSULTING SERVICES
10 - 15 Years
Multiple Locations

Posted on: 22/04/2026

Job Description

Job Summary :


We are seeking an experienced Technical Project Manager with deep expertise in the life sciences domain to lead and deliver complex technology implementations for our client.


This role requires a seasoned professional with 10+ years of implementation experience, strong technical acumen, and a proven track record in regulated environments.


The ideal candidate will ensure seamless deployment, integration, and optimization of client solutions while effectively managing stakeholder expectations and regulatory compliance.


Key Responsibilities :


- Project Leadership : Lead end-to-end implementation of client solutions, covering scoping, requirements gathering, configuration, testing, and go-live.


- Client Engagement : Serve as the primary point of contact, providing expert guidance, managing expectations, and ensuring successful solution adoption.


- Solution Configuration & Integration : Work closely with technical teams to configure solutions as per client requirements and ensure integration with enterprise systems.


- Data Migration & Validation : Define and execute data migration strategies, ensuring data accuracy, integrity, and compliance.


- Project Planning & Governance : Develop detailed project plans, including timelines, resource allocation, milestones, and proactive risk mitigation.


- Regulatory Compliance : Ensure all implementations adhere to global regulatory standards (FDA, EMA, GxP), with proper documentation for audits and compliance.


- Training & Support : Deliver client training, create user documentation, and provide post-implementation support to drive adoption.


- Continuous Improvement : Collaborate internally to enhance implementation methodologies, delivery efficiency, and client satisfaction.


Required Qualifications :


Education :


- Bachelors degree in Life Sciences, Computer Science, Information Systems, or related field.


- PMP or relevant certifications preferred.


Experience :


- 10+ years in software implementation (SaaS preferred).


- Minimum 5 years in life sciences (pharma, biotech, MedTech).


Technical Expertise :


- Experience implementing SaaS platforms in regulated environments; familiarity with regulatory systems (RIMS or similar) is highly desirable.


Project Management :


- Proven ability to manage complex programs using tools such as Azure DevOps, JIRA, or MS Project.


Regulatory Knowledge :


- Strong understanding of FDA, EMA, GxP, and related compliance standards.


Communication Skills :


- Excellent stakeholder management with the ability to translate technical concepts for diverse audiences.


Problem Solving :


- Strong analytical and troubleshooting capabilities with a solution-oriented mindset.


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