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Regulatory Associate Temporary

Lilly İlaç

İstanbul(Asya)

İş Yerinde

İş Yerinde

Job Type

Full-Time

Position Level

Specialist

Department

Health / Medical

Health / Medical

Application Count

273 application

Job Type

Full-Time

Position Level

Specialist

Application Count

273 application

Department

Health / Medical

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QUALIFICATIONS AND JOB DESCRIPTION


Lilly  İlaç Tic. Ltd. Şti is the Turkish affiliate of Eli Lilly and Company, one of the leading global pharmaceutical companies, with headquarters located in the Indianapolis, in the United States and a strong heritage of 140 years. Lilly operates in 120 countries with approximately 41.000 employees worldwide. 
We make medicines that help people live longer, healthier, more active lives. We strive for leadership in the therapeutic areas we have chosen: Diabetes, Neuro-Sciences, Oncology, Endocrinology and Men's Health.

We are looking for a temporary Regulatory Associate.

 

  •  Bachelor’s degree in health sciences (pharmacy, chemical and medical).
  •  Minimum 2 years of related experience in pharma industry
  •  Ability to work in a regulatory environment both independently and within a team
  •  Ability to exercise judgement in accomplishing goals
  •  Good knowledge of regulations and guidelines
  •  Organizational skills and detail-orientation
  •  Ability to prioritize multiple tasks/projects.
  •  Strong knowledge of MS Word, Excel and Outlook
  •  Proficiency in English language both oral and written
  •  Availability for travel


İŞ TANIMI


 Provides regulatory expertise and executes the submission of the new products in the market (including product line extension, new indication), regulatory maintenance of marketed products (including product maintenance as manufacturing or labeling variations, renewals, etc.) aligning related written procedures.
 Work according to the company procedures and policies that assures consistent accurate and efficient processing of required submissions.
 Aligns global regulatory partners’ goals and objectives through appropriate database tools ensuring desired affiliate performance.
 Makes registration submission of GMP (good manufacturing practices).

 

Preferred Candidate

More than 2 years of experience
Bachelor’s(Graduate), Master’s(Student), Master’s(Graduate)
Completed
English(Reading : Advanced, Writing : Advanced, Speaking : Advanced)

Ruhsatlandırma Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Ruhsatlandırma Uzmanı Ruhsatlandırma Uzmanı Maaşları Ruhsatlandırma Uzmanı Nasıl Olunur? Ruhsatlandırma Uzmanı Nedir? Ruhsatlandırma Uzmanı İş İlanları

Pharmaceuticals industry

Hakkımızda

Lilly İlaç

Şirket Sayfasına Git

Ruhsatlandırma Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.

Ruhsatlandırma Uzmanı Ruhsatlandırma Uzmanı Maaşları Ruhsatlandırma Uzmanı Nasıl Olunur? Ruhsatlandırma Uzmanı Nedir? Ruhsatlandırma Uzmanı İş İlanları