Specialist in regulatory projects in YuRiYa-FARM, Farmacevtichna grupa kompaniy

YURIYA-PHARM is a Ukrainian pharmaceutical group of companies that owns the largest area of ​​production facilities in Ukraine. We already operate in more than 50 countries of the world and have ambitious goals to enter the TOP 100 global pharmaceutical companies.

Today, in the conditions of martial law, without stopping for a single day, we continue to provide both the civilian population and the armed forces with essential medicines and medical products.

We offer:

• official employment;
• competitive salary and annual performance bonus;
• safe and modern office, free food;
• laptop, corporate mobile phone;
• annual leave lasting 30 calendar days, instead of 24 according to the Labor Code;
• material assistance in various life situations;
• career growth and corporate development programs.

Functional duties:

• Management of regulatory projects on pharmaceuticals presence;

• Organization and conduct of certification/recertification//amendment procedures;

• Communication with the conformity assessment body/notification body: submitting applications, agreeing dates, audit format, signing the certification agreement and related documents;

• Preparation of documentation for audit;

• Conducting/participating in external audits;

• Development and updating of Tech file. 

Necessary knowledge and skills:

• Higher pharmaceutical/ industrial/ technological/ biotechnological education;

• Experience in medical device certification and technical file development;

• Knowledge of regulatory requirements;

• Experience of collection, systematization and analysisinformation;

• English - level intermediate or higher (ability to work with foreign clients and suppliers).