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İlan yayından kaldırılmıştır
İstanbul(Asya)
İş Yerinde
İş Yerinde
Job Type
Full-Time
Position Level
Specialist
Department
Research and Development (R&...
Research and Development...
Application Count
895 application
Job Type
Full-Time
Position Level
Specialist
Application Count
895 application
Department
Research and Development (R&D)
QUALIFICATIONS AND JOB DESCRIPTION
ILKO Pharmaceutical Inc., with more than 40 years of pharmaceutical experience is now expanding its product portfolio via developing biotechnological drugs.
ILKOGEN Biopharmaceutical Inc., that is the subsidiary of ILKO is the unique innovation company in Turkey with the scope of developing and manufacturing novel biotechnological pharmaceuticals as well as next generation biobetter and biosimilar products.
With this open position, ILKOGEN is looking for senior R&D specialist who has expertise in analytical method development for biotechnological pharmaceutical R&D.
Minimum Qualifications
• BS. degree in Chemistry or other related discipline and PhD. degree in molecular biology and genetics, biotechnology, cell biology, biochemistry or other related discipline.
• Minimum 2 years of experience in analytical process development and application for pharmaceutical protein products.
• Significant experience with the analysis methods used for determination of physiochemical, structural and biologic properties of proteins, in the frame of pharmaceutical protein characterization.
• High communication skills
• Analytical thinking and problem solving
• Working in an interdisciplinary environment
• Learning and adapting to new techniques easily
• Ability to work both cooperatively and independently
• Ability to design experiments, analyze data and troubleshoot
• Engage in high performance work teams
• Good time management
• Convenient for abroad travels for long periods
• Advanced English level (both verbal and written)
Preferred Qualifications
• Expertise or knowledge on IND (Investigational New Drug) application filing, to follow the analytic process required to obtain the approval for clinical trials.
• Expertise and knowledge on quality control process, including SOP and batch record documentation.
Preferred Candidate
More than 2 years of experience
Doctorate(Graduate)
Completed
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Şirketin Aydınlatma Metni
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ARGE Laboratuvarı Uzmanı ARGE Laboratuvarı Uzmanı Maaşları ARGE Laboratuvarı Uzmanı Nasıl Olunur? ARGE Laboratuvarı Uzmanı Nedir? ARGE Laboratuvarı Uzmanı İş İlanları