לוח משרות דרושים רפואה ופארמה בנתניה

Eitan Medical is a fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care - from the hospital to the home. Job Description: Managing the post market RA team which handles the following activities: · Support design and post market compliance of products from a regulatory perspective · Handling Vigilance, MDR and authorities’ inquiries of complaints · Support the investigation process from a regulatory perspective · Responsible for managing product field action · Responsible on regulatory assessment related QMS process · Responsible of company’s PSUR Direct manager: VP of RA and QA

a U.S.-based global leader in defence technology is seeking a Vice President of Quality to lead the companys quality strategy and organization. The Vice President of Quality is responsible for defining and executing the companys 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 companys 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 companys 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.

Managing the post market RA team which handles the following activities:

Support design and post market compliance of products from a regulatory perspective

Handling Vigilance, MDR and authorities inquiries of complaints

Support the investigation process from a regulatory perspective

Responsible for managing product field action

Responsible on regulatory assessment related QMS process

Responsible of companys PSUR

Direct manager: VP of R&A

The R&D Lab serves as a facility where test methods are conducted, and services are provided for the Research, V&V, Mechanics, and Investigation departments. The R&D-V&V Lab Student expected to perform routine laboratory duties as directed and to participate in the team missions in order to meet the department goals.

As a R&D-V&V Lab Student your primary responsibilities will include ,verification activities of new products design, including defining test requirements, collecting and processing laboratory test samples, environmental monitoring and testing guidelines in accordance with SOPs and CGMP regulations.

You will execute all general tests and V&V tests in the R&D Lab, including data collection and analysis.

You will participate in departmental tasks that include problem solving and critical/root cause analysis.

From time to time, you might be asked to join interesting field work at third parties /sub-contractors' sites.