Looking for an experienced IT Business Partner to support CMC operations from regulatory writing through tech operations to manufacturing. This is a unique opportunity to lead projects, optimize processes, and work directly with internal teams and external vendors.
What You’ll Do
* Act as the internal anchor, leading IT-enabled projects across CMC and biologics manufacturing.
* Map business processes, identify pain points, and find ways to automate and digitize workflows.
* Improve internal reporting and ensure data from external manufacturers is accurate and efficient.
* Challenge vendors and guide RFPs while partnering with internal stakeholders (Tech Ops, Quality, Regulatory).
* Support regulatory reports, ensuring alignment with global specs and leveraging technology to streamline manual processes.
What We’re Looking For
* Experience in biologics and outsourced manufacturing.
* Background in big pharma or consulting (PwC, Deloitte, Accenture, etc.).
* Strong business acumen first, IT knowledge second.
* Proven ability to make decisions, own projects, and drive execution.
* Comfortable working in workshops and collaborating across multiple teams.
* Innovative mindset with a focus on process improvement and automation.
Why This Role is Exciting
* Be the internal lead that drives change and reduces reliance on external consultants.
* Work on projects that directly impact global regulatory compliance and manufacturing efficiency.
* Collaborate with a dynamic, cross-functional team and external vendors to shape the future of CMC data management.
This is a full-time contract role (1.0 FTE, 40 hours/week)
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