IMP Qua­li­ty Cli­ni­cal Pack­a­ging

Vollzeit @Flex­sis veröffentlicht 11 Stunden ago

Job-Beschreibung

EIN­FÜH­RUNG:

Flex­sis is part of the Inter­i­man Group, one of the lea­ding pro­vi­ders of per­son­nel ser­vices in Switz­er­land. Thanks to our solid exper­ti­se and the com­pe­ten­ces within the Inter­i­man Group, we offer tail­or-made solu­ti­ons in per­son­nel con­sul­ting.

For our cli­ent F. Hoff­mann — La Roche in Kai­ser­augst , we are loo­king for a moti­va­ted and relia­ble (m/f/d)

IMP Qua­li­ty Cli­ni­cal Pack­a­ging 100%

AUF­GA­BEN­BE­SCHREI­BUNG:

  • Sup­port all qua­li­ty-rele­vant pack­a­ging pro­ces­ses and col­la­bo­ra­te with pack­a­ging ope­ra­ti­ons and all rele­vant inter­faces with regard to GMP topics
  • Part­ner with stake­hol­ders and pro­vi­de GMP sup­port to ensu­re suc­cessful deli­very of the com­pa­ny goals
  • Review and release of manu­fac­tu­ring spe­ci­fi­ca­ti­ons and Batch Records (BR) of finis­hed and semi-finis­hed goods
  • Mana­ge actively Devia­ti­ons and Chan­ges
  • Col­la­bo­ra­ti­on through to the manage­ment of local and glo­bal pro­jects
  • Actively enga­ge in opti­miza­ti­on acti­vi­ties and impro­ve­ments within IMP Qua­li­ty Cli­ni­cal Pack­a­ging Switz­er­land. Coor­di­na­te impro­ve­ment pro­jects and enga­ge in cor­rec­ti­ve and pre­ven­ti­ve mea­su­res (CAPA)
  • Build, veri­fy and imple­ment stan­dard docu­ments (SOPs)
  • Joy in a human-cen­te­red and self-mana­ged way of working based on New­Work, with a key focus to sup­port the ongo­ing cul­tu­ral and orga­niza­tio­nal chan­ge towards col­la­bo­ra­ti­on, agi­li­ty and inno­va­ti­on mind­set

ERFOR­DER­LI­CHES PRO­FIL:

  • Min. Mas­ter Degree pre­fer­a­b­ly in Life Sci­en­ces or Engi­nee­ring or simi­lar degree
  • Min. 3 years of expe­ri­ence in the phar­maceu­ti­cal indus­try in a qua­li­ty mana­ger role
  • Know­ledge of cGMP and qua­li­ty requi­re­ments for cli­ni­cal deve­lo­p­ment pha­ses
  • Expe­ri­ence in the area of phar­maceu­ti­cal deve­lo­p­ment such as pack­a­ging lines or mate­ri­als, mas­ter data manage­ment, qua­li­ty con­trol or qua­li­ty assu­rance is an advan­ta­ge
  • Pro­ven track record to work towards out­co­mes and an inno­va­ti­ve man­ner of sol­ving pro­blems
  • Strong team-play­er with a high level of self-moti­va­ti­on and being able to inspi­re others
  • Abili­ty to work in a pur­po­se dri­ven orga­niza­ti­on, taking full owner­ship for assi­gned roles and tasks, con­ti­nuous­ly wil­ling to impro­ve indi­vi­du­al and team effec­ti­ve­ness
  • Abili­ty to com­mu­ni­ca­te cle­ar­ly and pro­fes­sio­nal­ly ver­bal­ly and in wri­ting in BOTH Ger­man and in Eng­lish is a must.
  • Expe­ri­ence with SAP and Veeva is a plus

Start date: asap — latest: 01.08.2025
Plan­ned dura­ti­on: 12 months
Exten­si­on: pos­si­ble
Remote/Home Office: Min. 80% onsite

Are you inte­res­ted and would you like to sei­ze this oppor­tu­ni­ty? Then we should defi­ni­te­ly get to know each other! Sim­ply click on “App­ly now” and we look for­ward to recei­ving your com­ple­te appli­ca­ti­on docu­ments.

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