Regulatory Affairs Specialist

The Regulatory Affairs Specialist works in the pharmacy division. Preparation of registration portfolios – including checking that contents are according to regulations, writing consumer manuals, designing packaging, attending to changes/renewal/updates including stringencies with manuals, and supporting all activities in the pharmacy division.

Responsibilities
Field of responsibility

Preparation of all types of submissions –products, renewals, variations, leaflets and packaging.
Responsibility for maintaining up-to-date product regulatory dossier.
Direct contact with the Ministry of Health and partners abroad.
Conducting regulatory and document checks.
דרישות התפקיד
Requirements
Required education and experience

Bachelors degree in pharmacy or other life science degree (chemistry/biology)
Previous experience of at least 2 years in regulatory affairs in Israel registration/renewal/variations of pharmaceutical products
High standard of English.
Extremely high standard of Hebrew.
Proficient in Microsoft Office - Outlook, PPT, Word, Excel.
Required qualification

Accurate.
Ability to work under pressure.
Energetic and hardworking.
Trustworthy.