Regulatory Affairs Officer Setúbal

Regulatory Affairs Officer
Setúbal
Setúbal, Setubal, Portugal

Do you want to participate in the sustained growth of a certified ISO 9001:2015 company that values honor, professional ethics, integrity, loyalty, honesty, and courage? Are you looking for dynamism, satisfaction in your work, and recognition for your efforts? Join us!

ZEMIR PHARMA CONSULTING - Your Career Opportunity

Regulatory Affairs Officer

Your Job Responsibilities:

1. Providing regulatory affairs support to our clients.
2. Managing Marketing Authorization (MA) applications.
3. Handling variations and renewals of MAs.
4. Translating regulatory procedures for submission to authorities.
5. Developing readability tests and bridging reports.
6. Preparing clinical and
   - clinical reports.
7. Processing price and reimbursement applications.
8. Ensuring compliance.

Additional Responsibilities for Medical Devices, Cosmetics, and Food Supplements:

1. Writing technical dossiers.
2. Developing instructions for use and labeling.
3. Notifying competent authorities.
4. Maintaining compliance.

Candidate Profile:

• Graduate degree in Pharmaceutical Sciences or other life sciences.
• At least 2 years of experience in Regulatory Affairs.
• Excellent communication skills and ease of expression.
• Proficiency in spoken and written English.

How to Apply:

If you are interested in joining our ZEMIR PHARMA team for this challenging opportunity, please send your application documents, including your earliest possible starting date, via Linked
In or to ******.

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