דרושים בתחום רפואה ובריאות

המשרה פונה לנשים וגברים כאחד

Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
We are seeking for an experienced scientist (PhD) to join the pharmacology department. The successful candidate will direct research for drug development in the pharmaceutical industry.
Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
The position requires knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
Experience in the discipline of translational medicine, laboratory animal science, veterinary medicine, are an advantage.
Duties and responsibilities:
Design and implement pharmacology strategy and studies (in vitro & in vivo) for drug candidates in development
Work with internal and external resources (outsourcing & expert consultants) to execute investigation plan
Write scientific protocols, reports,
Communicate findings to scientific and non-scientific audiences
Provide input on pharmacological aspects for new candidates either internal or external (via due diligence,)
Support and write regulatory submissions/interactions
Support scientific discussions, communications and publications (self and third party initiated)

PhD/PostDoc level
Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
Strong interpersonal and management skills
Excellent communication skills;
Excellent English (oral , written)
Industry experience, R&D focus areas highly desired, development of biological products is an advantage

To plan, budget, oversee and document all aspects of the specific project you are working on.
Coordinating with cross-functional team members to make sure that all parties are on track with project requirements, deadlines, and schedules.
Meeting with project team members to identify and resolve issues.
Submitting project deliverables and ensuring that they adhere to quality standards.
Preparing status reports by gathering, analyzing and summarizing relevant information.
Establishing effective project communication plans and ensuring their execution.
Coordinating the development of user manuals, training materials and other documents as needed to enable successful implementation and turnover of the process or system to the users.
Identifying and developing new opportunities for cost reduction and process improvement.
Obtaining users acceptance of project deliverables.
Managing users satisfaction within project transition period.
Conducting post project evaluation ("lesson learned") and identifying successful and unsuccessful project elements.
Working in global environment: o Interacting with PhV local reps. around the world
o Interacting with other PhV global functions
o Interacting with other departments in Teva like PhV-IT, QA & Regulatory affairs
Taking part in the development and maintenance of an efficient and robust Pharmacovigilance system.

Education:
*MSc or BSc in chemistry or biochemistry, with at least two years of relevant experience, or technician with at least ten years of experience in the relevant field

Knowledge/Skills Requirements:
*Experience and knowledge in analytical methods for glycoproteins and in particular in HPLC/UPLC. Knowledge in mass spectrometry is advantage
*Basic knowledge in GLP/GMP guidelines
*Good team work capabilities
*Hebrew- fluent, English- reading and writing
*Proficiency in use of computers for technical writing, data collection, data analysis and presentation