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Required an Associate Director Medical Affairs.
Responsibilities:
- Budget Planning and Resource Management.
- Hires, manages, coaches and develops a group of Medical Affairs Managers/MSLs assigned to his/her therapeutic areas to ensure the highest quality scientific exchange in alignment with the Medical Affairs plan.
- Collates Medical Affairs Manager/MSL field insights that will be shared internally as appropriate.
- Provides input into the therapeutic area Medical strategy led by the local Medical Affairs Managers.
- Ensures that there is adequate and compliant cross-functional collaboration between the Medical Affairs Managers/MSLs and internal stakeholders.
- Organizes regular team meetings for relevant trainings, sharing of best practices, reinforcing on compliance matters and discuss therapeutic area strategies.
- Develop his/her Medical affairs managers/MSLs functional and scientific skills.
- Establishes the annual performance objectives for his/her team.
- Conducts mid-year and year-end reviews of team performance.
- Develops and maintains up-to date scientific knowledge around relevant disease areas, products within those areas and research methodologies.
- Ensure optimal scientific leader management and support
- Develop medical strategy (including the Medical Affairs plan, MAPs)
- Align medical strategy with business unit/franchise-needs with marketing
- Responsible for the creation and timely execution of all Medical activities in his areas of responsibility including medical education, data generation activities etc...
- Responsible for close follow ups on all systems updates of the activities under his responsibility.
- Review and approve s MSL plans.
- Collaborate with GCTO and Market access around new products.
- Ensures that all Medical Affairs Managers/MSLs perform their duties in alignment with company SOPs/Guidelines and local laws and regulations.

Required a Medical Affairs Manager.
Responsibilities:
- Developing local clinical trial strategy for the therapy are in the country and taking appropriate action
to ensure proper implementation.
- Establishing, managing and owning local Key Opinion Leader (KOL), investigator, and other key stakeholder relationships in the therapy area(s).
- Advising business units on medical and scientific matters in the therapy area(s).
- Providing input into local study feasibility and site selection.
- Implementing publication policy for the therapy area(s).
- Giving medical input into market access/access alliance.
- Providing medical and scientific advice to business units, market access/access alliance functions and others as required, as well as input into Health Economics.
- Providing medical and scientific training to the field force, Global Clinical Operations and others as required
- Developing local clinical research programs and clinical trial strategies.
- Designing local study protocols and support operations.
- Providing input into global clinical research programs and trial/protocol design.
- Performing activities related to local Medical Research and MA.
- Advising business units on medical and scientific matters, includingbut not limited toscientific approval of promotional materials.
- Identifying licensing opportunities.
- Building, managing and owning relationships with local KOLs and other key stakeholders.
- Training and scientific support for these and all parts of the company.
- Providing scientific support for continuous medical education (CMEs).
- Ensuring compliance with all applicable country regulations.
- Overseeing all local MA activities in the therapy area(s).
- Generating study concepts with KOLs.
- Developing Protocol Concept Sheets (PCS) and obtaining Protocol Review Committee (PRC) and global Strategic Review Committee (SRT) approvals for new local studies.
- Enhancing the company reputation and profile through an external focus, by representing the company on cross-company boards.

Required a Medical Affairs Manager Oncology.
Responsibilities:
- Developing local clinical trial strategy for the therapy are in the country and taking appropriate action
to ensure proper implementation.
- Establishing, managing and owning local Key Opinion Leader (KOL), investigator, and other key stakeholder relationships in the therapy area(s).
- Advising business units on medical and scientific matters in the therapy area(s).
- Providing input into local study feasibility and site selection.
- Implementing publication policy for the therapy area(s).
- Giving medical input into market access/access alliance.
- Providing medical and scientific advice to business units, market access/access alliance functions and others as required, as well as input into Health Economics.
- Providing medical and scientific training to the field force, Global Clinical Operations and others as required
- Developing local clinical research programs and clinical trial strategies.
- Designing local study protocols and support operations.
- Providing input into global clinical research programs and trial/protocol design.
- Performing activities related to local Medical Research and MA.
- Advising business units on medical and scientific matters, includingbut not limited toscientific approval of promotional materials.
- Identifying licensing opportunities.
- Building, managing and owning relationships with local KOLs and other key stakeholders.
- Training and scientific support for these and all parts of the company.
- Providing scientific support for continuous medical education (CMEs).
- Ensuring compliance with all applicable country regulations.
- Overseeing all local MA activities in the therapy area(s).
- Generating study concepts with KOLs.
- Developing Protocol Concept Sheets (PCS) and obtaining Protocol Review Committee (PRC) and global Strategic Review Committee (SRT) approvals for new local studies.
- Enhancing the company reputation and profile through an external focus, by representing the company on cross-company boards.

Required a Medical Affairs Manager.
Responsibilities:
- Developing local clinical trial strategy for the therapy are in the country and taking appropriate action to ensure proper implementation.
- Establishing, managing and owning local Key Opinion Leader (KOL), investigator, and other key stakeholder relationships in the therapy area(s).
- Advising business units on medical and scientific matters in the therapy area(s).
- Providing input into local study feasibility and site selection.
- Implementing publication policy for the therapy area(s).
- Giving medical input into market access/access alliance.
- Providing medical and scientific advice to business units, market access/access alliance functions and others as required, as well as input into Health Economics.
- Providing medical and scientific training to the field force, Global Clinical Operations and others as required
- Developing local clinical research programs and clinical trial strategies.
- Designing local study protocols and support operations.
- Providing input into global clinical research programs and trial/protocol design.
- Performing activities related to local Medical Research and MA.
- Advising business units on medical and scientific matters, includingbut not limited toscientific approval of promotional materials.
- Identifying licensing opportunities.
- Building, managing and owning relationships with local KOLs and other key stakeholders.
- Training and scientific support for these and all parts of the company.
- Providing scientific support for continuous medical education (CMEs).
- Ensuring compliance with all applicable country regulations.
- Overseeing all local MA activities in the therapy area(s).
- Generating study concepts with KOLs.
- Developing Protocol Concept Sheets (PCS) and obtaining Protocol Review Committee (PRC) and global Strategic Review Committee (SRT) approvals for new local studies.
- Enhancing the company reputation and profile through an external focus, by representing the company on cross-company boards.

The EMEA Business Continuity Planning (BCP) and Emergency Response Coordinator will provide hands-on subject matter expertise and leadership in support of Applied Materials global business continuity and emergency response program.
This position will collaborate with individuals from all departments globally to implement, maintain, and execute the business continuity and emergency response programs for Applied Materials in Israel and Europe.

Implementation of policies and procedures to ensure that Quality. System Regulations (e.g.: FDA Part 820 Quality System Regulation, ISO 13485 Quality Standard) .
Develop, modify, apply and maintain quality procedures, work instructions and protocols.
Conduct investigations and lead corrective/preventive action planning and problem solving efforts.
Conduct material, component, and equipment qualifications
Conduct internal audits.
Provide input to engineering, production, and materials to ensure compliance with procedure, regulations, and standards.
Utilize statistical analysis and recognized quality tools (FMEA, risk analysis, hypothesis testing, and root cause analysis) .
Lead as the QA/Compliance responsible through the different project phases.
Evaluate and approve the qualification documentation, i.e. URS, GxP-Risk Assessment, Validation plan, IQ, OQ, PQ.