Business Analyst for Digital Systems

Biosimilar Sciences PR LLC

16h•Onsite

About The Position

Company: OcyonBio is a partnership development and manufacturing organization focused on advancing gene and cell therapies. OcyonBio provides dedicated autonomous manufacturing capacity with interconnected infrastructure and systems to support phased-appropriate development from early development through pre-clinical, clinical, and commercial stages. We operate as a cGMP incubator environment with full regulatory systems capabilities and resources to generate CMC data supporting global regulatory applications. Our manufacturing and development spaces are designed to function autonomously while remaining fully integrated with the systems required to support clinical and commercial operations. We are committed to fostering a workplace free of explicit and implicit discrimination and harassment, where every individual feels safe, heard, and valued. The character of our employees is as important as their talent, and we’re proud of the team and environment we’re assembling as we grow. Place of Performance: CII George Sanders, Aguadilla Pueblo, Aguadilla P.R. 00603. Job Overview: OcyonBio is seeking a Business Analyst to serve as the internal subject matter expert (SME) to support and evolve our digital manufacturing ecosystem, including L7 ESP, MES, and LIMS systems. This role bridges business operations and IT, ensuring that our systems are effectively implemented and configured, continuously improved, and aligned with manufacturing, quality, and regulatory needs. The ideal candidate will work closely with Manufacturing, Quality, IT and other to design, configure, and optimize workflows while ensuring compliance with regulatory standards. This position is open to both hands-on with systems and capable of understanding business processes, with the potential to grow into a system owner and subject matter expert within the organization.

Requirements

Bachelor’s degree in Business, Information Systems, Engineering, Life Sciences, or a related field (or equivalent experience)
Experience in business analysis, systems implementation, or process improvement is preferred but not required
Exposure to MES, LIMS, ERP, or similar enterprise systems is a plus
Experience in pharmaceutical, biotechnology, or regulated environments is highly desirable but not required
Strong ability to understand and translate business processes into technical solutions
Interest in becoming a system owner and long-term SME within the organization
Understanding (or willingness to learn) of cGMP and FDA-regulated environments
Ability to work cross-functionally with technical and non-technical teams
Strong problem-solving and analytical thinking skills
High attention to detail and structured approach to work.
Business process analysis and workflow design
Systems thinking and troubleshooting
Clear communication and training facilitation
Documentation and requirements gathering
Adaptability in a fast-paced, startup environment

Nice To Haves

Basic understanding of databases, data flows, or system integrations (preferred)

Responsibilities

Become the internal SME for L7 ESP, MES, and LIMS platforms
Translate business and manufacturing requirements into system workflows and configurations
Design, configure, and optimize digital workflows within L7 and related systems
Provide ongoing user support, troubleshooting, and system guidance across departments
Facilitate system training sessions and develop user documentation
Collaborate with IT, Quality, Manufacturing, and external vendors to implement system improvements
Support system validation and ensure alignment with cGMP and FDA regulatory requirements
Identify opportunities for process automation and operational efficiency
Assist in change management and system adoption across the organization