Biopharmaceutical IT Specialist
3 days ago
Are you passionate about delivering cutting-edge solutions in the biopharmaceutical industry?
We are seeking an experienced IT Application Specialist to join our team at AGC Biologics.
About the RoleThis is a unique opportunity to leverage your technical expertise and business acumen to drive innovation and excellence in our IT operations.
- Manage Configured Screens and Fields: Ensure seamless integration of new features and modifications to existing configurations, aligning with customer needs and industry standards.
- PPM Configuration Expertise: Proactively manage and maintain Project Portfolio Management (PPM) configurations, ensuring optimal performance and user experience.
- Requirements Analysis and Recommendations: Collaborate with cross-functional teams to gather requirements, analyze, and provide actionable recommendations for product updates, ensuring alignment with current vision.
In this role, you will be responsible for:
- Assisting in Test Planning and Execution: Contribute to the creation, revision, and execution of test plans, functional testing, or application testing during rollout, ensuring high-quality delivery.
- Maintaining Reporting and Integration: Develop and maintain reporting for PM's and management, as well as create and monitor integration with external applications.
- Managing Permissions and Users: Oversee permissions, end-users, and integration users, adhering to JSOX requirements.
- Providing Issue Resolution and Support: Assist with issue resolution and post-implementation support, ensuring timely and effective issue resolution.
You will work closely with business and vendor stakeholders to implement the system, managing customer expectations regarding scope, schedule, and budgetary parameters. You will also identify impacts across teams and coordinate across senior levels to manage dependencies and potentially competing priorities.
About AGC BiologicsAGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO), committed to delivering the highest standard of service as we work side-by-side with our clients and partners. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide.
The estimated salary for this position is around $80,000 - $110,000 per year, depending on experience and qualifications.
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