Senior Manager GLP/GCP Veeva Doc Control and Training

About the role

Sana Biotechnology is growing, and we are hiring new team members who believe in the potential of engineered cells as medicines, who are passionate about delivering the possible to patients, and who lead with the desire to work on novel ideas. As a Sr Manager Veeva Doc Control and Training you will report to the Executive Director Global GCP/GLP and QA. This person will be responsible for formatting, review, issuance, and control of procedures, work instructions, forms, and test methods throughout the organization. The Sr. Manager will also help maintain all employees' training files and curriculum, to ensure employees remain current in assigned training.

What you’ll do

• Responsible for the end-to-end lifecycle of documents in Veeva.
• Provide customer support to authors and approvers regarding creation, reviewing, revising, and obsoleting procedural documents.
• Advise cross functionally to identify document type, impacted stakeholders, and review cycle including conflict resolution and approval.
• Identify (with stakeholders) document changes that impact regulations and escalate to appropriate owner or quality assurance.
• Work with cross functional t...