Quality Director

**Your mission**:
As we successfully progress on this exciting journey and actively prepare the company for entry into the clinical stage, we are searching for a Quality Director (m/w/d) to play a pivotal role in establishing and managing an innovative pharmaceutical quality system, including point-of-care activities.

This activity is instrumental in facilitating and expanding the adoption of our groundbreaking products in hospitals worldwide.

**Responsibilities**:
Lead the foundations and operations of NVision’s cGXPs quality system, managing the two sides of our innovative use case:

- Quality processes for the development, manufacturing, control, and distribution of NVision’s imaging injectable agents, as well as the devices and reagents necessary for their compounding following the applicable regulatory and pharmaceutical quality requirements in the USA and EU.
- Quality processes for point-of-care operations supporting healthcare professionals who utilize our technologies. These processes align with the innovative decentralized manufacturing framework currently built by health agencies worldwide.

This mission plays a crucial role in executing NVision’s ambitious strategy and will be accomplished through the following steps:

- ** Building and leading an efficient Quality Assurance Team**: this involves team creation, development, coaching, and mentoring, as well as performance and project management.
- ** Providing oversight of the Quality Assurance Department**:ensuring that quality management systems and operations align with the company goals and deliver robust and effective results. This compliance extends to all applicable regulatory and quality requirements in the USA and EU for pharmaceuticals.
- ** Designing Innovative Quality Programs and Modalities**: develop quality tools that enable decentralized manufacturing at the point of care, in hospitals. These initiatives can be based on software tools such as ALM/eQMS or integrated solutions within NVision devices, in partnership with NVision’s development team.
- ** Onboarding health agencies and hospital users** during the implementation of these innovative quality approaches, supported by the CMC and Regulatory Affairs Department.
- ** Regulatory Compliance and Audits**: prepare the organization for regulatory inspection audits. Ensure that all necessary documentation, procedures, and personnel comply with standards, working closely with the CMC and Regulatory Affairs department.
- ** Supplier and Partner Oversight**:oversee the assessment and qualification of suppliers and partners, and guarantee the reliability and compliance of subcontracted components, materials, and services.
- ** Leading Quality Excellence**: spearhead efforts to establish and maintain a culture of quality excellence across NVision, with a focus on innovation, continuous improvement, risk mitigation, patient safety and customer satisfaction.
- ** Environmental and HS Compliance**:collaborate with the Manufacturing Operations to ensure NVision’s product compliance with environmental and health, safety, and environment (HSE) regulations.

**Your profile**:

- At least 10 years of hands-on experience in quality assurance, with a demonstrated ability to lead quality operations, specifically within the pharmaceutical, radiopharmaceutical, or drug-device combination sectors, in both EU and US markets.
- Demonstrated ability to build and deliver a cGXPs quality system in the context of company/activity creation, product development, and/or company transformation.
- Proven track record in leadership roles, driving quality excellence, impactful results, and onboarding of internal and external stakeholders.
- Innovation mindset: comfortable in a startup environment, where problem-solving skills, organization skills, agility, and innovation are prized.
- Familiarity with electronic Quality Management Systems (eQMS) and Application Lifecycle Management (ALM) for contracting, integration, and operational management.
- Working in an international, interdisciplinary, and cross-functional team: experience collaborating with a diverse group of strong scientific and development experts.
- Qualified Person (QP) possibility: proven track records, or the possibility to act as a QP in Germany, is considered an advantage.

**Why us?**:

- Competitive compensation, based on base salary and stock options
- Hybrid remote possible (Our offices and labs are located in Ulm, Germany.)
- Key role in a highly advanced and fast-growing startup company
- Ample opportunity for personal initiatives, openness to new ideas and room for considerable personal impact
- Impactful product promoting better understanding and treatment of disease
- International team, from over 15 different nationalities
- Enjoyable work atmosphere with an open-door and open communications mentality
- Indefinite employment contract, providing stability
- Long-term career growth opportunities
- 30 vacation days and excelle