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Take on a pivotal role as a Regulatory Affairs Specialist in Israel, supporting both pre-market and post-market regulatory activities within our companys Diabetes spin-off organization. In this role, you will be a key partner to cross-functional teams, ensuring regulatory compliance across the product lifecycle while enabling timely market access and sustaining ongoing business operations. This is an exciting opportunity to contribute to a growing, agile organization focused on innovation and delivering impactful solutions for people living with diabetes.
This position is an exciting opportunity to work with our company's Diabetes business. our company has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across our company, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.
Responsibilities may include the following and other duties may be assigned:
Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and inspections.
Leads or compiles all materials required in submissions, license renewal and annual registrations.
Recommends changes for labelling, manufacturing, marketing, and clinical protocol for regulatory compliance.
Monitors and improves tracking / control systems.
Keeps abreast of regulatory procedures and changes.
May direct interaction with regulatory agencies on defined matters.
Recommends strategies for earliest possible approvals of clinical trials applications.

DRS RADA Technologies, a leading defence company specializing in the development and production of advanced tactical radar systems, and part of Leonardo DRS — a U.S.-based global leader in defence technology — is seeking a Vice President of Quality to lead the company’s quality strategy and organization. The Vice President of Quality is responsible for defining and executing the company’s quality strategy across the entire product lifecycle — from design and development through production, delivery, and sustainment. This role ensures that all systems and products meet the highest standards of reliability, compliance, and customer satisfaction expected in the defence industry. As a member of the executive leadership team, the VP of Quality leads the company’s quality organization and partners closely with R&D, Production, Supply Chain, and the Lines of Business to drive excellence in design, manufacturing, supplier performance, and operational execution. The role also includes ongoing collaboration and reporting to the corporate organization of our U.S.-based parent company, requiring strong communication, alignment, and cross-company partnership skills. Key Responsibilities
* Lead the company’s Quality and Productivity organization, reporting to the GM.
* Define and implement quality systems and standards across all business areas.
* Drive continuous improvement, yield enhancement, and root-cause analysis processes.
* Ensure compliance with defence industry standards, customer requirements, and corporate quality policies.
* Maintain certifications and regulatory compliance and oversee audits and corrective actions.
* Foster a culture of accountability, precision, and excellence across the organization.