לוח משרות דרושים רפואה ופארמה עבודה זמנית

we offer hope to patients suffering from rare and severe diseases by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead, and work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve. We are a dynamic, fast-paced company, operating in over 25 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us! As a QP Pharmacist, you will be Responsible for ensuring compliance with all ongoing control processes designed to guarantee that products are not released to the market until it is determined that their quality matches the approved specifications in the registration file. In addition, responsible for quality processes in the regulatory affairs department that will be adapted to international standards, local regulations, where applicable, and the organizational quality level established for medical products. This is a temporary position for 8 months.
Responsibilities:

* Qualified Person Responsible Pharmacist of the importer.
* Ensuring Compliance with Israeli Regulations: The QP is responsible for ensuring that all pharmaceutical products meet the standards set forth by Israel's Ministry of Health (MoH) and other relevant regulatory authorities. Review the product batch release documentation and authorizing or rejecting the batch release to the market. Certification of Compliance: to certify that each batch of the product has been produced and tested according to relevant specifications and regulations before it reaches the market.
* Accompanying regulatory audits and being responsible for regulatory knowledge, document control, writing procedures, maintaining and updating relevant professional literature, and assisting in planning training activities in the field.
* Liaison with the MOH and working according to the MOH guidelines, including immediate reporting of any complaint or recall if necessary.
* Responsible for batch releases of registered and non-registered products.
* Review PQRs and full batch records provided by the partners.
* Execution of additional supervisors instructions and tasks accordingly.

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