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Analytical Development Executive (Senior specialist or Chief of department) (LOCATION: TBILISI, GEO), Київ

ФАРМА ПЕРСОНАЛ www.pharma-personnel.com.ua
Вакансия добавлена 14.02.2023 21:01 , действительна до 31.12.2024

“ФАРМА ПЕРСОНАЛ”- специализированное рекрутинговое агентство.

«ФАРМА ПЕРСОНАЛ»- спеціалізоване агентство

 

Роботодавець:   Грузія, Тбілісі, фармкомпанія-виробник лікарських засобів

 

FUNCTIONS:

The primary function for this position is to oversee and participate analytical development’s daily activities, such as method development and validation, analytical testing and stability program.

 

RESPONSIBILITIES

  • Supervise a group of analytical development scientists, and give guidance in their method development and validation, analytical testing, process support, stability and product evaluation.
  • Review method validation plans and reports to assure that the methods meet requirements during different phases of product development.
  • Direct activities and design experiments toward troubleshooting/optimization of existing analytical methods when necessary.
  • Assure accurate and timely testing and reporting all results, issuing technical reports which include certification and validation data.
  • Provide guidance on analytical investigations of abnormal results.
  • Work in collaboration with other departments, e.g. Process, Formulations, Regulatory Affairs, Production, Supply Chain, etc, to support timely new product development and submissions.
  • Work with contract laboratories and collaborators.
  • Participate in selection, evaluation and development of new personnel.
  •  

QUALIFICATIONS

  • PhD or Master Degree in Chemistry, Pharmaceutical Sciences or related fields. Master with over 8 years of experience and PhD with over 3 years of experience in the pharmaceutical analytical chemistry.
  • Working knowledge of major analytical techniques. Ability to train scientists on new techniques.
  • Strong experience with analytical development in pharmaceutical development, including method development, validation, stability and in-process control within CMC.
  • Familiar with pharmaceutical industry regulations and EMA/FDA/ICH guidelines
  • Proven supervisory experience.
  • Good analytical skills in sorting information, formatting directions and problem solving.
  • Good communication skills and English language ability.

 

Пропозиція компанії: оговорюється індивідуально

Ваше резюме надсилайте за адресою: ustimenko@ph-p.com.ua

Тел.: (067) 900 88 75 Оксана

Контактное лицо: Оксана Устименко
Мобильный телефон: (067) 900-88-75


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Вакансия добавлена 14.02.2023, действительна до 31.12.2024

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