Regulatory Affairs Officer Viseu

Regulatory Affairs Officer
Viseu
Viseu, Viseu District, Portugal

Do you want to participate in the sustained growth of a certified ISO 9001:

2015 company that believes in the values of honor, professional ethics, integrity, loyalty, honesty and courage?

You look for dynamism, satisfaction in what you do, and be appreciated for what you do?

Join us!

ZEMIR PHARMA CONSULTING is your career opportunity.

Regulatory Affairs Officer

Your Job

Regulatory affairs support to our clients.

Medicines

Management of Marketing Authorisations (MA) Applications.

Management of variations and renewals applications to MAs.

Translations of regulatory procedures to be submitted to Authorities.

Development of readability tests/bridging reports.

Development of clinical/non-clinical reports.

Price and reimbursement applications.

Compliance.

Medical devices, Cosmetics and Food Supplements

Technical dossier writing.

Development of instructions for use and labeling.

Notification to competent authorities.

Compliance.

What we are looking for in your profile

Graduate degree in Pharmaceutical Sciences or other life sciences degree.

With at least 2 years' experience in Regulatory Affairs.

Ease of expression and contact.

Proficiency in spoken and written English.

How to apply?

If you are interested in joining our ZEMIR PHARMA team taking over this challenging job opportunity in our
- oriented company, we are looking forward to receiving your application documents stating your earliest possible starting date.

Please send your application via Linked
In or to ******.

Personal data collected for recruitment purposes will be used solely for that purpose, as defined in our
General Data Protection Policy.