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Open nowPosted 10 hours ago

Senior Projektledare inom läkemedelsutveckling

Avaron AB

Where
Södertälje, Stockholms län, Sweden
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Your applicationOpen nowSenior Projektledare inom läkemedelsutvecklingAvaron AB · Södertälje, Stockholms län, Sweden

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Avaron AB's own form.

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.7%14 days
  5. 35.6%30 days
  6. 58.0%60 days
This job: posted 10 hours ago

The posting

Om företaget Hos Avaron får du tryggheten i en fast anställning kombinerat med variationen av att arbeta ute hos olika kunder. Vi tillsätter specialister inom allt från teknik, IT och industri till projektledning och affärsstöd – och oavsett uppdrag har du en konsultchef som finns där för dig och din utveckling. Om rollen Flera utvecklings- och tillverkningsprojekt pågår parallellt, och nu förstärker vi teamet med en erfaren konsult. Du hjälper till att ta fram en tillverkningsprocess för en läkemedelsprodukt, och sedan blir du en del av tillverkningsteamet som tillverkar produkten i klassade lokaler enligt GMP. Uppdraget är hos RISE, ett oberoende statligt forskningsinstitut som arbetar med tillämpad forskning och test- och demonstrationsanläggningar för att stärka näringslivets konkurrenskraft. Du får vara med från processutveckling hela vägen till tillverkning. Uppdraget omfattar upp till 100 % av heltid. ArbetsuppgifterDu utvecklar tillverkningsprocessen för en läkemedelsprodukt tillsammans med projektteamet. Du är med i tillverkningsteamet när produkten tillverkas i klassade GMP-lokaler. KravDu har minst 5 års erfarenhet av GMP. Du har minst 5 års erfarenhet av läkemedelsutveckling. Du har minst 6 års erfarenhet av arbete inom läkemedelsindustrin. Du har dokumenterad erfarenhet från läkemedelsproduktion eller processutveckling i en GMP-reglerad miljö. MeriterandeDu har minst 2 års erfarenhet av Med.tech kvalitetssystem. Du har minst 4 års erfarenhet av utredningar inom GMP. Du har haft en ledande roll i projekt. Vi erbjuderFast anställning hos Avaron AB Tjänstepension Friskvårdsbidrag på 5 000 kr per år Ansökan Vi tillsätter löpande – sök gärna så snart du kan.

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