Quality Systems Manager

Vor Bio•Boston, MA

8h•Remote

About The Position

At Vor, we believe science can do more than manage symptoms. It can change the course of disease. By advancing telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, we are silencing upstream survival signals and stopping downstream autoimmune cascades. Together, we are addressing disease at its root cause and rewriting what is possible for patients worldwide. When you join Vor, you’re not just working on a medicine. You’re part of a mission to redefine the future of autoimmune care. Why Work at Vor? Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases. Growth: Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond. Innovation: Work on a platform with potential beyond one indication — a therapy that has already shown consistent results across lupus, IgA nephropathy, and Sjögren’s syndrome. Belonging: Join a culture where every voice is heard, and where our shared mission unites us across functions and geographies. POSITION: Quality Systems Manager The Quality Systems Manager will be responsible for overseeing and ensuring compliance with current Good Practices (GxP) for applicable GxP systems, including document management (EDMS), training (LMS) and the electronic quality management system (eQMS). This role will coordinate and execute document management activities in an effective and compliant manner. This role will also provide training and maintain training compliance of all applicable stakeholders that impact clinical and commercialization activities. Additionally, this role will collaborate with internal and external teams, ensuring alignment of quality standards and the timely execution of all deliverables. The individual will possess a strong hands-on expertise in GxP quality systems and operations within the biotech industry.

Requirements

Bachelor's degree in Life Sciences, Engineering, or a related field.
Minimum 3-5 years of experience in quality systems, quality assurance, document management/training management within the biotechnology or pharmaceutical industry.
Expertise in GxP, regulatory requirements, and industry best practices (FDA, EMA, ICH).
Ability to collaborate with cross-functional teams and complex initiatives.
Excellent knowledge of quality systems, documentation, and compliance management.
Exceptional problem-solving, troubleshooting, and analytical skills.
Strong communication and presentation skills, both written and verbal.
Ability to work effectively with communication and office tools in a remote, fast-paced, and evolving environment.

Nice To Haves

Experience with Phase 3 clinical trials and the transition to commercialization is highly preferred.

Responsibilities

Perform document control duties to manage the creation, review, approval, revision, obsoletion, and storage of GxP documents (SOPs, Work Instructions, Policies, etc.) and records. Additionally, this role may require QA review of other records and deliverables.
Responsible for the ongoing management of the electronic Document Management System (eDMS).
Experience with systems for processing Deviations, Change Controls, Audits, CAPAs, Investigations, Vendor Management, Complaints, etc. Additionally, evaluate system functionality, evaluate new features from periodic releases and assist with the implementation of value added features.
Oversee the training process to maintain compliant training for GxP stakeholders.
Support the establishment of training curricula and training materials.
Track completion rate of training of stakeholders.
Responsible for the ongoing management of the training system.
Serve as the Corporate Training Coordinator and support day-to-day Corporate Document Management and Training activities, including ensuring corporate documents are maintained in the appropriate system and assigned correctly to support broader business needs.
Support regulatory inspections and audit requests (FDA, EMA, etc.).
Support the implementation, maintenance, and reporting of quality metrics and KPIs to ensure alignment with company objectives.
Prepare materials for Quality Management Review meetings, including KPI summaries, quality reports, and trending analyses to support management oversight and continuous improvement.
Partner with IT, CMC, Supply Chain, Clinical Operations, Clinical QA, Biometrics, Regulatory Affairs, and other GxP teams to implement procedures, training, quality activities, and ensure quality compliance throughout the document and product lifecycle.
Assist with the coordination of periodic SOP Committee meetings with various departmental leadership.