Quality Assurance
2 weeks ago
Vi på Randstad Life Sciences utökar och nu söker vi nya kollegor. Vi söker dig som har jobbat ett par år inom kvalitetssäkring. Vi har en stor kundportfölj, över hela Mälardalen, med tyngd inom läkemedelsbranschen. För att kunna täcka upp för våra kunders olika behov söker vi nu dig som har gedigen erfarenhet.
Vi är lyhörda till dina önskemål kring uppdrag och arbetsuppgifter och i och med vårt breda kundportfölj i Mälardalen kommer vi tillsammans att anpassa din fortsatta karriär utefter din kompetens, erfarenhet och ambition. På Randstad Life Sciences har vi ett erbjudande som innebär att du har möjlighet att kompetensutveckla dig och/eller ta ut extra ledighet efter att du varit en tid hos oss.
Konsulter på Randstad får en trygg anställning med fast lön, kollektivavtal och förmåner som friskvårdsbidrag, tjänstepension, försäkringar och företagshälsovård. Tillsammans med oss får du möjlighet att utvecklas och bredda din kompetens genom att vara ute på spännande uppdrag hos våra kunder
Ansvarsområden
Exempel på arbetsuppgifter kan vara:
- Hantera kvalitetsrelaterade frågor
- Vara stöd vid framtagande samt godkänna avvikelseutredningar/CAPA och ändringsärenden
- Säkerställa att arbetsprocesser och dokumentation uppfyller ställda krav
- Ansvara för release av råvaror/slutprodukt
- Sätta upp kvalitetssystem
- Vara ”bollplank” i QA-frågor som rör aktuellt område
- Agera som QA-representant och/eller projektledare
- Utbilda andra inom aktuellt område
Kvalifikationer
Vi söker dig med erfarenhet av kvalitetssäkringsarbete.
Det är viktigt att du har:
- Några års erfarenhet av självständigt QA-arbete
- Gedigen kunskap i relevanta regelverk som GMP/GAMP5 och/eller medtech ISO13485 eller motsvarande för aktuellt område
- Har en högskole- eller universitetsexamen inom naturvetenskap (apotekare, civilingenjör, Msc, PhD)
- Minst 7,5 p Mikrobiologi samt erfarenhet av Steril/Aseptisk tillverkning
- Har mycket goda kunskaper i svenska och engelska i tal och skrift
- Meriterande med kunskap i validering/kvalificering/datoriserade system
Egenskaper som är viktiga i denna roll är att du är noggrann, strukturerad och har god samarbetsförmåga. Som person är du social och nyfiken. Andra viktiga egenskaper för att trivas och lyckas i rollen som konsult är flexibilitet och möjlighetsorienterad. Vidare krävs att du har förmåga att sätta dig in i nya situationer samt att hantera flera frågeställningar samtidigt. Du har även förmåga att kunna arbeta självständigt och på eget initiativ. Vi fäster stor vikt vid personlig lämplighet.
Skicka in din ansökan senast 2024-09-22. Urval och intervjuer kommer att ske löpande. Tjänsten kan komma att bli tillsatt innan sista ansökningsdag, ansök därför så snart som möjligt. Vi kan på grund av GDPR inte ta emot ansökningar via e-mail.
ansvarsområden
Exempel på arbetsuppgifter kan vara:
- Hantera kvalitetsrelaterade frågor
- Vara stöd vid framtagande samt godkänna avvikelseutredningar/CAPA och ändringsärenden
- Säkerställa att arbetsprocesser och dokumentation uppfyller ställda krav
- Ansvara för release av råvaror/slutprodukt
- Sätta upp kvalitetssystem
- Vara ”bollplank” i QA-frågor som rör aktuellt område
- Agera som QA-representant och/eller projektledare
- Utbilda andra inom aktuellt område
kvalifikationer
- Några års erfarenhet av självständigt QA-arbete
- Gedigen kunskap i relevanta regelverk som GMP/GAMP5 och/eller medtech ISO13485 eller motsvarande för aktuellt område
- Har en högskole- eller universitetsexamen inom naturvetenskap (apotekare, civilingenjör, Msc, PhD)
- Minst 7,5 p Mikrobiologi samt erfarenhet av Steril/Aseptisk tillverkning
- Har mycket goda kunskaper i svenska och engelska i tal och skrift
- Meriterande med kunskap i validering/kvalificering/datoriserade system
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