Process Development Document Specialist (Contractor)

About Us…
Obsidian Therapeutics is pioneering engineered cell and gene therapies to deliver transformative outcomes for patients. Obsidian’s programs apply our cytoDRiVE® technology in Cell and Gene therapy products to control expression of proteins for enhanced therapeutic efficacy and safety. Obsidian’s lead program is currently in clinical development for the treatment of patients with metastatic melanoma and non-small cell lung cancer.
We’re proud of our diverse talented team and committed to cultivating an environment of inclusion where each person feels a strong sense of belonging and is supported to continuously learn and contribute their best work. Our Research team is based in the heart of Cambridge, MA, and Technical Operations team is based in our purpose built facility in Bedford, MA. Obsidianites enjoy a highly collaborative culture, competitive salary and benefits, and potential for ownership through stock options.
Our Opportunity......
We’re looking for a motivated, detail-oriented, and efficient Process Development Document Specialist, with a background in process characterization or quality documentation to join our team for a 6 month contract engagement. You’ll work closely with the Process Development team to support completion of multiple development and characterization reports and other documents, helping to drive the development of our first clinical stage autologous cell therapy program targeting solid tumors.
In this role, you’ll perform data verification, assist with formatting documents, maintain an always current status tracker, and work closely with Document Control to drive documents through the review and approval process to meet project timelines.
As a member of our Technical Operations team, you will be a vital part of a highly collaborative group working to unlock the promise of precision cell therapy for patients, starting with our lead program amsoki-cel (OBX-115), a novel engineered tumor-infiltrating lymphocyte (TIL) cell therapy that uses our proprietary cytoDRiVE® platform. This is a unique opportunity to be a valuable contributor in a well-funded clinical company with field-leading advisors, best-in-class partners, and an experienced team.
This is a hybrid role; including time on site in our Bedford, MA office as needed.
You Will....
Core responsibilities
Support completion of process characterization reports and other process development documents working closely with authors.
Perform Data Verification to ensure accuracy in reports.
Assist with formatting of documents.
Work with the manager and Process Development team to establish a document tracker. Keep tracker up-to-date with status of each document and communicate with all authors and PD management.
Work closely with Document Control, including submission of Document Change Request forms as needed
You Bring...
Core Qualifications
BS or BA in a life sciences field
4+ years of relevant experience in biotech/pharma, preferably Process Development (PD), Analytical Development (AD), Quality Control (QC), Quality Assurance (QA).
Working knowledge of cell biology and/or engineering.
Proven ability to work with high attention to detail
Excellent planning, coordination, and time management skills
Working proficiency with Microsoft Word and Excel, and willingness to learn and use other system.
Excellent oral and written communication skills. You listen to understand and communicate effectively and persuasively with partners and colleagues.
Ability to build and maintain productive relationships with colleagues within functional team and across the organization.
Collaborative and accountable – recognizes success requires teamwork and interdisciplinary thinking; shares feedback and ideas to facilitate better outcomes
Self-motivated, with a proven ability to meet objectives, timelines, and high standards managing multiple responsibilities in parallel.