About this role
Student Assistant, Global IT Compliance
Help strengthen quality and compliance in a regulated IT environment
Do you enjoy structure, documentation and working with details that matter? As Student Assistant in Global IT Compliance, you will support key compliance and quality processes in a regulated IT environment.
This role is a strong opportunity for a student who is organized, eager to learn and interested in how IT compliance, quality management and operational excellence come together in practice.You will work closely with Global IT Compliance and Validation specialists, IT project teams and subject matter experts, helping maintain high standards for documentation, process control and follow-up.
A role close to documentation, quality and process control
You will support the team in maintaining and updating controlled documents in the Document Management System. This includes helping document owners with revisions, approvals and lifecycle management.
You will also assist with tracking, coordinating and closing CAPAs, as well as supporting the creation, monitoring and follow-up of Change Controls. An important part of the role is helping ensure progress, structure and timely escalation when actions or deadlines are at risk.
Supporting projects and SOP development
As part of Global IT Compliance, you will collaborate with IT and IT Compliance colleagues on ongoing projects. You will help follow up on task status, deliverables and action items, contributing to structure and momentum across different activities.
You will also support the development, review and rollout of Standard Operating Procedures. This includes coordinating input from stakeholders, helping ensure alignment and maintaining SOP tracking, version control and communication.
What will help you succeed
You are comfortable working in a changing environment where priorities may shift. You adjust quickly to new information, processes and requirements, and you enjoy bringing order and follow-up to ongoing tasks.
We imagine that you:
• Are detail oriented and highly organized.
• Work effectively with different team members and stakeholders.
• Approach challenges with curiosity and a willingness to learn.
• Can manage multiple tasks and follow up independently.
• Have an interest in compliance, quality management or regulated environments.
• Are currently enrolled in a Bachelor’s or Master’s program within IT, Business, Engineering, Compliance or a related field.
Ready to take the next step?
Please submit your application through our recruitment system. We do not receive CVs by email.
Please submit your application via our careersite.
Who We Are
AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in Denmark. From our Søborg site, we develop and manufacture life‑changing advanced biologics for some of the world’s most innovative pharmaceutical companies. Together with our team members across Europe, the U.S., and Japan, we deliver development and manufacturing of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells therapies. Across our global network, we are united by one mission: To work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.
About AGC Biologics
Global contract development and manufacturing organization (CDMO) for biopharmaceuticals and cell/gene therapies. Based in Seattle, WA.
Similar jobs you might like
