דרושים ביוטכנולוגיה

B.Sc or M.Sc (in relevant field such as biology, chemistry, biotechnology etc.)High level of English (written and spoken)QA auditor, with 2 or more years of experience in a GMP pharmaceutical companyExperienced in the QA activities (GMP audits, CAPA, chan

PROTALIX is a leading pharmaceutical company in the biotechnology industry, located in Carmiel.

Protalix is a publicly traded (NYSE, TASE:PLX), clinical stage biopharmaceutical company focused on the development and commercialization of recombinant therapeutic proteins using its proprietary ProCellEx™ plant cell culture protein expression system. ProCellEx™ provides a unique platform on which we have established a pipeline of proprietary and next-generation versions of recombinant therapeutic proteins, relying upon known biological mechanisms of action.


This is an opportunity for you to join our talented and highly successful team. As you will be working with the best, we require an individual who is professional in his work and dedicated to providing excellent scientific and regulatory support to the business. This is a critical role as it requires effective collaboration with both internal and external customers.

As a Product Development Project Manager you are responsible to coordinate and support the development of a new product from the R&D stage through preclinical and clinical development and regulatory stages. .

Your main responsibilities will be:
 Understanding the scientific background and mechanisms of relevant products/ molecules
 Providing input into development and review of regulatory materials/ documents for scientific accuracy and compliance with relevant regulations and codes of practice
 Pro

For you to be successful in this role you will meet the following criteria:
 PhD in Life Science
 At least 2 years experience in the biopharmaceutical industry
 Outstanding level of written and spoken English
 High level of attention to details, project and time management skills
 Good interpersonal skills and communication skills
 Self-starter with ability to work independently and in teams
 Experience in the following areas: CMC and/or preclinical development preferably with protein drugs, regulatory affairs of drug development