לוח משרות דרושים מכשור רפואי

As a medical representative, you will promote the company's products in the regions of the country: Center - South - Jerusalem.

Communicate with professional HCPs (physicians, nurses, pharmacists) in a variety of channels F2F and digital.

The medical representative will raise product awareness, answer queries, provide updated and reliable information, and introduce new products.

Responsibilities


Territory and customer management: MCCP update, Call plan adherence (CPA), identifying customer needs, and suitable channels for communication.
Organizing F2F appointments and meetings with HCPs.
Support HCP's decision to optimize patient outcomes in an ethical way.
Lecture to physicians and medical personnel (according to the MC terms).
Promoting the company's products
Raise awareness of the unit's products and scientific updates (EBM).
Meeting both the business and scientific needs of healthcare professionals.
Development of new initiatives.
Creating collaborations and establishing professional relationships with HCPs.
Active participation in team meetings, including sharing information and best practice, reading relevant materials, and preparing presentations and marketing materials according to the team's needs.
Open communication with customers and company functions regarding the team products.
Maintain a deep and current knowledge of the industry, trade association, competitors, and buyer dynamics and focus effort on customer opportunities.
Working according to the company's practices, compliance codes, rules, and regulatory guidelines.
Report any safety information received during work to the Pharmacovigilance Department.
Attending conferences in Israel and overseas at any time required

We are looking for a Design Quality Engineer.
The Design Quality Engineer is responsible for driving exceptional product quality for the patient safety, customer value beyond expectations, regulatory assurance, and optimized Cost of Quality for the Company. This is a key technical position, affecting part quality for both installed base and NPI products.
AS a Design Quality Engineer (DQE) you will plays a crucial role in ensuring the safety, efficacy, and regulatory compliance of medical equipment including cooperated with the design and development team, and apply quality management principles throughout the product life cycle.
DQE's main responsibilities include:
Review design documents and specifications, to ensure that they meet relevant standards and regulations
Participant in risk assessment, identify and reduce potential risk quality
Take part in the design and verification process

Job Description As a Quality Assurance Leader, you will be responsible for conducting Afimilk’s day-to-day product quality activities. Your role is to ensure that Afimilk’s final products adhere to the established quality standards. Your responsibilities encompass conducting routine and quality inspections, identifying, and resolving workflow and production issues, training, investigating customer complaints, performing supplier evaluations and audits, and review of product specifications and quality control plans. Essential Duties and Responsibilities include the following (Other duties may be assigned):
* Day-to-day quality engineering activities such as product quality documentation, incoming inspection, customer complaints, , product deviation, non-conformities, Document control and fields corrective action
* Conducting incoming inspection and evaluating the compliance of products or with requirements, specifications, or standards.
* Conducting audits at manufacturers and subcontractors, performing source inspections according to specified drawing/work instructions and quality requirements.
* Managing quality processes in the manufacturing, including monitoring, and controlling processes, preparing quality reports and analyses, and maintaining relevant documentation.
* Conducting quality inspections on suppliers and incoming raw materials to the factory and ensuring their compliance with required quality standards.
* Responsible for leading and implementing IPQC, IQC, OQC approval to supplier.
* Establishing metrics and criteria for monitoring suppliers and subcontractors. · Collaborate with Operations, R&D QA, Engineering and Manufacturing functions to ensure quality standards are in place. · Validation of manufacturing process to meet targets, production output and quality standards.