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offers 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.

offers 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!

We are hiring PV Associate.
Monitoring and reporting adverse events and safety information, ensuring compliance with regulatory safety guidelines and conducting activities to monitor and enhance the safety profile of products
Responsibilities
Receiving, translating, processing and documenting any reports, from overseas or locally, regarding adverse events and safety information of products in compliance with regulatory requirements
Submitting timely and accurately safety reports to the Ministry of Health in compliance with local regulatory requirements
Actively following-up on adverse events reported by physicians and patients
Collecting and reviewing safety and efficacy measures taken by health authorities in recognized countries. This includes monitoring publications, regulatory updates, and safety communications from agencies such as the FDA, EMA, and other global health organizations to ensure compliance and up-to-date safety practices for products
Reviewing relevant data from the scientific literature related to drug safety. This includes conducting literature searches to identify new safety information, adverse events, and emerging safety issues
Promoting awareness among healthcare professionals and medical teams regarding the importance of reporting adverse events to ensure public safety
Conducting periodic internal and external reconciliations
Assisting in preparation for PV audits and inspections
Conducting PV trainings to employees and external suppliers
Additional tasks as defined by the manager

Medison offers 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 want to make a difference in people's lives, we invite you to join us! The product manager will be responsible for fully managing the commercial aspects of the product- strategy, budgeting, and business plan, including its execution, and checking if it meets its target. Working closely with overseas partners, having an in-depth understanding of the field, and KOL's. The role combines working in the field, implementing and monitoring unique projects, and working at the office. It also combines managing the field force.

Responsibilities:

* Full ownership of the products, leading them to sales targets
* Collect in-field,cross-functional, and market analysis data and synthesize insights and stakeholders’ behavior and drivers
* Work with a cross-functional team to build a strategic business cross-functional plan based on strategic objectives and define KPIs
* Build a tactical plan including innovative tactics and omni-channel plan to meet strategic objectives
* Execute tactical plan according to KPIs, objectives, and timeline, and monitor it.
* Prepare & execute a budget plan.
* Build and manage a territory plan and monitor it.
* Management of field force, including KPIs setting, planning and monitoring field work, employees development, and recruitment to handle complex field projects.
* Project Management: Identifying and driving critical projects that generate exponential growth
* Develop marketing material for in-field use in collaboration with the partner and according to local regulatory requirements.
* Working with the medical manager to analyze scientific data and present to stakeholders
* Troubleshoot and objection handling.
* Work in accordance with the company code of ethics and guidelines laid down by the regulatory department.
* Work with the internal team to find solutions to get things done in a simplified way.
* Business meetings with overseas partners, training sessions, conferences, etc
* Participation in conferences in Israel and abroad according to strategic priorities.

Are you ready to make a difference in the world of healthcare? At AstraZeneca, we are committed to pushing the boundaries of science to deliver life-saving medicines that transform patients' lives. As a Medical Advisor in the Cardio Vascular therapeutic area, you will play a pivotal role in shaping the performance of AstraZeneca's brands. You will be at the forefront of building scientific partnerships with Key External Experts (KEE) and healthcare professionals, driving strategic and educational medical affairs projects, and providing essential medical input to marketing, sales, and market access teams. This dynamic role combines office-based work with significant field presence, allowing you to continuously build robust scientific expertise and contribute to the medical therapeutic area strategy.

Accountabilities:
Conduct scientific exchange and collect customer insights:
- Stay up-to-date in TA knowledge through active monitoring of scientific literature, congress attendance, and interactions with Key External Experts (KEE).
- Lead pre-launch medical strategy and initiatives to address current gaps.
- Discuss key data sets with experts to identify patient pathways and treatment realities.
- Build relationships with experts for advocacy development.
- Brief speakers for scientific events.
- Respond to unsolicited requests for information about unapproved AstraZeneca products or uses.
- Continuously improve impactful communication skills.
- Interact with other Medical Advisors/MSLs and MAMs to exchange best practices.
Deliver Key medical leadership into the brand strategy:
- Work in strategic partnership with Marketing and Market Access Department.
- Provide high-quality scientific and medical input in Brand Teams and strategic projects.
- Review and approve promotional material with thorough understanding of standards.
- Develop and execute medical affairs projects according to budget and timelines.
- Coach and support MSLs to ensure development and execution of MSL Action Plans.
Maintain top-notch robust scientific and medical expertise:
- Keep track of relevant scientific literature in the TA.
- Attend international and national scientific congresses.
- Engage with KEE in the TA.
- Ensure excellent up-to-date scientific knowledge among internal colleagues.
- Support Clinical operations in site selection.
Manage scientific partnerships with KEE:
- Manage Externally Sponsored Research.
- Follow-up on grants/chairs/scientific sponsorings with KEE.
- Organize and lead meetings with KEE for input on data sets or projects.
Be compliant:
- Successfully complete all training requirements.
- Comply with external regulations & internal policies.

A pioneering med-tech company developing innovative inhalation technologies for precise drug delivery. Our mission is to enhance patient care by leveraging breakthrough technology to improve treatment outcomes.

We are looking for a cQP (Cannabis Qualified Person) & cRP (Cannabis Responsible Person) to join our Tiberias site. As cQP (Cannabis Qualified Person) youll ensures that each batch of product released for marketing is produced and tested in accordance with the quality and regulatory requirements.

As cRP (Cannabis Responsible Person) youll be responsible for drugs inventory movements in the facility and for fulfilling regulatory requirements. Moreover, ensures that each batch of product released for marketing is produced and tested in accordance with the quality and regulatory requirements.
Key Responsibilities
Responsibilities as cQP
Releasing cartridge production batches to the market after approval of quality assurance, ensuring compliance with regulatory and quality requirements, adhering to Eudralex volume 4, annex 16, guidelines.
Batch release approval documents will be personally kept by the CQP, available for authorities review, for a period of no less than 5 years.
Supervision of the production of cannabis products.
Change controls regarding manufacturing process review and, when applicable, plan approval.
Participation in solving quality issues and deviations in production.

Responsibilities as cRP
Contact with the relevant district pharmacist on issues related to the production or release of products.
Dangerous Drugs inventory log management.
Dangerous Drugs annual report to the IMCU: Preparation of annual reports for submission to the district pharmacist.
Control over the receipt of cannabis into the warehouse.
Supervising the preparation of shipments of finished products.
Preparation of rejected cannabis for destruction including full documentation.
Carrying out a monthly and annual cannabis inventory count.
Change controls regarding inventory management and procedural cannabis movements review and, when applicable, plan approval.
Control of procedures as needed.

Medison offers 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! We are hiring PV Associate. Monitoring and reporting adverse events and safety information, ensuring compliance with regulatory safety guidelines and conducting activities to monitor and enhance the safety profile of Medison’s products

Responsibilities:

* Receiving, translating, processing and documenting any reports, from overseas or locally, regarding adverse events and safety information of Medison’s products in compliance with regulatory requirements
* Submitting timely and accurately safety reports to the Ministry of Health in compliance with local regulatory requirements
* Actively following-up on adverse events reported by physicians and patients
* Collecting and reviewing safety and efficacy measures taken by health authorities in recognized countries. This includes monitoring publications, regulatory updates, and safety communications from agencies such as the FDA, EMA, and other global health organizations to ensure compliance and up-to-date safety practices for Medison’s products
* Reviewing relevant data from the scientific literature related to drug safety. This includes conducting literature searches to identify new safety information, adverse events, and emerging safety issues
* Promoting awareness among healthcare professionals and medical teams regarding the importance of reporting adverse events to ensure public safety
* Conducting periodic internal and external reconciliations
* Assisting in preparation for PV audits and inspections
* Conducting PV trainings to Medison’s employees and external suppliers
* Additional tasks as defined by the manager

Are you passionate about making a difference in the lives of people living with Obesity? Do you have a knack for building impactful strategies and fostering meaningful relationships? If so, we invite you to join our company as our new Obesity Consumer Engagement Product Manager. Read on and apply today for a life-changing career!
The position
As an Obesity Consumer Engagement Product Manager at our company, you will play a key role in transforming people living with obesity experience care and support. This is your opportunity to lead meaningful change by putting patients at the heart of everything we do. You will drive new and innovative ways to establish focused strategy to reach out people living with Obesity and Patients already on our innovative obesity treatments. Through cross-functional collaboration and a patient-first mindset, youll be at the forefront of launching impactful initiatives that support both individuals and the healthcare ecosystem.
Your main responsibilities will include:
Leading the launch excellence of anti-Obesity medication, ensuring a smooth and impactful introduction to the market for patients.
Crafting and executing an integrated engagement strategy tailored to the needs of people living with obesity.
Designing strategic communication plans and building meaningful partnerships to increase awareness and impact.
Collaborating with the medical community through scientific dialogue and supporting updates to medical guidelines.
Driving market access efforts, aligning with key stakeholders and payers to ensure broader availability of our treatments.

Are you passionate about ensuring the highest quality standards? Do you have a keen eye for details? We are seeking a Qualified Person (QP) to join our team and help us maintain excellence in our quality management processes. If this sounds like you, read more and apply today for a life-changing career!
The Position
As our Qualified Person you will perform batch release of clinical trial and marketed products in compliance with Ministry of Health (MoH) regulations, in collaboration with Clinical Trials and Commercial Supply Chain teams. You will report directly to Senior QP & PV Manager.
Additionally, you will:
Oversee importation, re-packaging, and quality-related documentation for non-registered products.
Review and maintain quality agreements and SOPs, ensuring alignment with regulatory standards and global procedures.
Investigate and manage deviations, including handling of reports of temperature excursions from pharmacies, hospitals, and distributor premises.
Review Annual Product Reviews (APRs) and support continuous quality improvement activities across the supply chain.

Are you ready to kick-start your career in clinical research with a global healthcare leader? Do you have a passion for ensuring clinical trials run smoothly from the very beginning? Would you like to grow in an innovative environment where your contributions truly matter?
If you answered yes, apply now for the Junior Clinical Start Up Specialist position at our company!
The Position
As our Junior Clinical Start-Up Specialist you will play a vital role in clinical research. You will manage start-up activities for clinical trials, ensuring compliance with local regulations, good clinical practice, our company procedures, and protocol requirements. Your work will focus on delivering reliable data and protecting study participants as you activate trial sites before the first patient visit in the country. Additionally, you will be responsible for executing regulatory submissions, including clinical trial applications, and ensuring timely approvals.
In addition, you will:
Prepare and submit Clinical Trial Applications to Health Authorities and Ethics Committees, ensuring compliance with local regulations, trial protocols, and applicable guidelines
Follow up on submissions until approvals are obtained, and collaborate with teams to answer queries and provide necessary documentation
Maintain effective communication with Health Authorities and Ethics Committees, ensuring all trial team members are informed of submission status and timelines
Manage document translations and approvals, including Clinical Trial product labels and directions for use
Ensure timely updates in the Vault Regulatory Information Management system, maintain confidentiality, and comply with company policies and regulatory requirements.