Regulatory Affairs Specialist

SUN PHARMA · Haïfa

🇬🇧 English

Microsoft Office

Job description

About the role

Taro-sun pharma is looking for a motivated Regulatory Affairs Specialist to join its R&D and Regulatory Affairs Department. You will play a key part in ensuring that our products meet all regulatory requirements throughout their lifecycle.

Key responsibilities

Prepare regulatory submissions and registration dossiers for the FDA and other international markets.
Respond to deficiency letters and inquiries from regulatory authorities.
Submit and manage post‑approval product variations and changes.
Support regulatory compliance activities across the product lifecycle.

Required profile

Bachelor's degree in Pharmacy, Life Sciences, or a related field.
Previous experience in regulatory dossier submissions and registrations (advantage).
Excellent English communication skills, both written and spoken.
Strong organization, accuracy, and attention to detail.
Ability to work effectively in a team and collaborate with cross‑functional stakeholders.

Required skills

Proficiency in Microsoft Office applications.

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Published 1 month ago

Expires 1 day from now

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SUN PHARMA

Haïfa

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