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במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.

מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.

חברה בתחום פארמה וביוטק

כפר סבא

חברה בתחום פארמה וביוטק

כפר סבא
מלאה

As our Regulatory Affairs Specialist, you will be responsible for all registration activities related to new drugs applications and product life cycle management, including review and approval of promotional materials to Health Care Professionals. You will be reporting directly to Senior Regulatory Affairs Manager.

You will also:
Ensure full compliance with us and IL Ministry of Health regulations.
Responsibility for the preparation, approval and proofreading of packaging materials.
Maintenance of our internal regulatory affairs systems.
Fostering effective collaboration within the team and with internal and external stakeholders.

Requirements:
To be successful in this role, you should hold a Bachelors degree in pharmacy and a strong understanding of pharmaceutical regulations and practices.

Additionally, you must have:
At least 2 years of experience in regulatory affairs within the pharmaceutical industry.
Strong communication and teamwork skills.
Excellent attention to details while working on multiple tasks.
Good computer skills.
Fluent Hebrew and English Verbal and written.

This position is open to all candidates.