Pracovní náplň
Reporting internally on product quality complaints and adverse events
Solving escalations and special cases for the Eastern European cluster
Management of incoming information flows regarding reports from stakeholders
Close cooperation with the Legal and Regulatory Affairs departments for country-specific issues
Setting up standardized answers for frequently asked questions in collaboration with Medical Advisors and Medical Science Liaisons.
Požadujeme
Mature personality with great communication skills
Good project management and organisational skills
Fluent English is a must, any other world language is a huge plus
Degree in pharmacy, biochemistry, chemistry or other life sciences or equivalent work experience
Pharmaceutical field work experience is a plus, but not a must
Nabízíme
An opportunity to gain experience in the pharmaceutical industry
Intensive training on the job to help you ease into your new role
Motivating remuneration
Possibility to work almost remotely or in a hybrid work model
5 weeks of holidays
Salary compensation for up to 15 days of sickness a year
10 fully paid care leave days
Generous cafeteria contribution
Engagement activities in the workplace
Kontakt - zadavatel pozice
ManpowerGroup s.r.o.Odpovědná osoba: Lucie Hlaváčková Telefon: Zobrazit tel. číslo Mobil: Zobrazit tel. číslo Email: zaslat email Web: http://www.manpower.cz
Adresa:
Na Florenci 2116/15
Praha 1
110 00
Další volná místa práce v Praze a okolí (1692)
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