לוח משרות דרושים רפואה ופארמה ביקום

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Medical Science Liaison is the extension of the medical function in the field. They build and develop enduring win-win' relationships with healthcare professionals and institutions, creating constructive partnerships with internal and external stakeholders to generate insights. MSL is executing the field medical activities that are aligned and integrated to the overall medical strategy within the Vaccines CSE MCO.

Main responsibilities:

Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products.
Actively engages with appropriate stakeholders on medical, clinical, epidemiologic, and scientific topics during an one-on-one interactions and group settings, to advance their understanding of the disease by sharing information and answering questions based on approved material within Regulatory guidelines.
Effectively utilizes the Scientific Engagement Model to plan territory and individual stakeholder (Key Opinion Leaders, payers, HCP etc.) medical strategy and engagement interaction plans consistent with the Field Base Medical Activity Plan and medical function priorities.
Supporting external lecturers in delivering balanced, non-promotional knowledge about therapeutic areas and our products.
Participating in the development and implementation of educational programs to improve the daily practice of healthcare professionals.
Organize and run external scientific events for our company about relevant disease or therapeutic topics.
Attending conferences and scientific symposia in the relevant therapeutic area.
Provide scientific support to the commercial team as necessary.
Collect key insights about the market, competitors, therapies, and customers.
Actively participate in on-going capabilities building sessions to improve medical knowledge, soft skills, and technical skills

As Customer Engagement Manager you will oversee implementing the companys strategy in the respiratory field, designing customer journeys and leading KOL engagement plans. Key focus should also be given to optimize execution of messaging, channel mix and digital innovation.

We are an innovative global healthcare company with a focus on immunology that extends to innovation in diabetes and transplant medicine. Across different countries, our talented teams are determined to deliver a best-in-class customer experience using the best of digital, artificial intelligence and personal know-how.

Main responsibilities:

Multichannel Engagement Strategy:

Prepare and execute local strategic and operational plans with Marketing, Medical, and Customer Experience teams.
Develop channel requirements for GTMC and ensure effective multi-channel usage.
Align customer/brand value propositions with brand/GBU Glocal strategy.
Project Management:

Contribute to the Customer Experience network, ensuring programs and tools are harmonized.
Implement best practice content strategy with marketing.
Set up and monitor KPIs with GTMC.
Data-Driven Decision Making:

Analyze and share data monthly and quarterly to inform decisions.
Conduct ROI analysis on customer engagement strategies with GTMC.
KOL management:

Work in close collaboration with medical to ensure a seamless KOL engagement.
Manage collaboration with local Pulmonology & immunology scientific associations and ensure optimal local congresses plan execution
Education & Training:

Optimize processes and systems for a positive customer experience.
Train employees to meet customer expectations.
Communication & Collaboration:

Implement content roadmap provided by MCO brand lead.
Collaborate with local service colleagues and Customer Experience partner to enhance Customer Experience.
Agile Ways of Working:

Communicate policy, procedure, and service changes.
Foster continuous improvement and adaptability to digital tools

Join our Israeli Regulatory team as a Regulatory Affairs Manager and Appointed Pharmacist responsible for the registration and maintenance of Marketing Authorizations for medicinal products of assigned portfolio and related health regulated activities. You will be also involved in transversal regulatory activities in dedicated projects.

The team is involved in developing regulatory product strategies, leading regulatory efforts in the development stage and post marketing of drug products in the Israeli market.

Main responsibilities:

Serve as Appointed Pharmacist, responsible for all matters related to medical products as specified by the Ministry of Health
Ensure compliance with local Israeli regulations and requirements
Manage regulatory aspects of product lifecycle from development through post-marketing including:
- Define registration and maintenance plans
- Coordinate country dossier preparations
- Manage registration, renewal, and post-authorization variation processes
- Update product labels and packaging materials
- Contributing to the Global Regulatory Product Strategy
Review promotional and non-promotional materials for regulatory compliance
Implement processes and quality systems
Monitor changes in the regulatory environment in Israel
Build strong external network with Health Authorities and Trade Associations

Join us in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world.

As a Quality Assurance in Israel, you will ensure compliance with global quality standards through documentation management and process control. You will oversee training programs, monitor quality metrics, and manage local GxP subcontractor oversight. You will drive continuous improvement through risk management and quality audits to maintain the highest standards of quality assurance

Main responsibilities:

Support the maintenance of Country Quality documentation management system in compliance with global procedures and quality standards.

Deviation and Corrective-Preventive Actions (CAPA) management: maintain the process to manage deviations and CAPAs related to all GxP and health-regulated activities

Change Control management: maintain the process to manage the changes that may impact GxP or health-regulated process or operations by leading multidisciplinary exchanges and action plans when necessary

Training: organize and manage information sharing, training sessions or programs related to processes owned by the Quality unit for concerned country associates, according to our standards and regulatory requirements

Country Quality Review: Monitor the related Quality Program and Action Plan follow-up

Country Quality performance indicators (KPIs): periodically report country KPIs defined by Global Quality

Support Quality oversight of locally managed GxP subcontractors: ensure an appropriate quality oversight process of locally managed subcontractors

Quality risk management: Ensure that quality risks are properly managed within the country (identification, assessment, control, communication)

Organize and participate in self-inspections, internal audits and external audits of third parties (suppliers / distributors / carriers / etc.) in accordance with the approved annual plan.