Workplace: Laboratory for the Study of Mitochondrial Disorders

Time: 1,0 

Shift: one shift (40 hours per week)

Start date: by appointment

WHAT DO YOU WANT TO DO?

• To deal with molecular-genetic diagnostics of mitochondrial diseases and other rare hereditary diseases (nucleic acid isolation, PCR, sequencing - Sanger and NGS, electrophoresis, genotyping)

WHAT IS Awaiting You When You Join Our Team?

• Recruitment Contribution 10.000, - 
• Facilities of a large university hospital in the center of Prague
• Interesting work in a small team 
• Possibility of involvement in laboratory research projects
• Possibility of personal and professional growth and support of further education
• Stable and motivating salary
• 5 weeks of leave and 1 week of leave to secure personal affairs
• Possibility of accommodation for outside Prague
• Catering allowance in canteens or meal vouchers
• VFN preschool and suburban summer camps for employees' children
• Interesting extracurricular activities - joint sports events and others

WHO WE ARE LOOKING FOR?

• You have completed min. Secondary school medical education
• You have the professional and medical competence according to the Act 96/2004 Coll.
• You are a graduate or a seasoned pro - all of us have doors open
• Education in clinical genetics is an advantage
• You are manually skilled and precise in the work you do
• You are working with PC at user level 
• An active approach to work and responsibility is not strange to you 
• You are able to work alone and in a team
• You want to learn new things and are flexible
• Can you prove us moral and civil integrity (pure criminal record)

Let us know and come to us with us! 

Ing. Markéta Tesařová, PhD.

phone: 224 967 748, email: Marketa.Tesarova@vfn.cz