QC Analyst Microbiology hos CCRM Nordic i Göteborg
Utför miljöövervakning i renrum, provtagning, inkubation och mikrobiologiska tester. Kräver master- eller doktorsexamen i mikrobiologi, minst 1 års erfarenhet av miljöövervakning i renrum samt kunskap om cellkultur och mikrobiologiska tester. Kräver flytande engelska.
Titel, arbetsplatsens namn och sammanfattning skrivna av AI utifrån annonsen.
Bra att veta
Lön
Inom yrkesgruppen Cell- och molekylärbiologer m.fl. har de som jobbar i privat sektor i hela landet i snitt 50 500 kr i månaden, varav 49 800 kr i grundlön. I hela landet, i privat sektor, tjänar hälften mellan 42 000 kr och 55 800 kr. Det är statistik för yrket, inte vad den här arbetsgivaren betalar.
Källa: SCB, lönestrukturstatistik 2025
Anställningen
Anställningen har inget slutdatum. Den kan börja med en provanställning på högst sex månader. Vill arbetsgivaren avsluta den under provtiden ska du få besked minst två veckor i förväg; annars blir den en vanlig tillsvidareanställning när provtiden är slut. Därefter krävs sakliga skäl för att säga upp dig, och uppsägningstiden är minst en månad, längre ju längre du har varit anställd.
Ett kollektivavtal kan ge andra regler än lagen.
Texten är skriven med AI och kan innehålla fel. Kontrollera med arbetsgivaren.
Källa: Lagen om anställningsskydd (LAS)
Arbetsgivaren
CCRM Nordic har annonserat 8 jobb det senaste året: 8 tillsvidareanställningar. Inom yrkesgruppen Cell- och molekylärbiologer m.fl. har de annonserat 2 gånger de senaste två åren, den här annonsen inräknad.
Källa: vår sammanställning av Arbetsförmedlingens annonser
QC Analyst - Microbiology
At CCRM Nordic, we are accelerating the development and commercialization of advanced therapies that have the potential to transform patients' lives. Our GMP facility and expert teams support the development and manufacturing of cell and gene therapy products, helping bring innovative treatments closer to the people who need them.
We are now looking for a QC Analyst Microbiology to join our Quality Control (QC) team at GoCo Health Innovation City. This is an exciting opportunity for someone with a strong microbiology background who thrives in a GMP-regulated environment and enjoys combining hands-on laboratory work with data review, investigations, and continuous improvement.
The role
As QC Analyst you will make sure our cleanroom environments and manufacturing operations meet GMP standards. You will run cleanroom environmental monitoring and sterility-related QC activities, help keep contamination control robust, and be the team's go-to person (subject matter expert) for microbiology. You will work closely with manufacturing during aseptic processing, contribute to investigations and continuous improvement, and give technical support to your QC colleagues.
Key responsibilities
- Carry out cleanroom environmental monitoring (EM): viable, non-viable, surface and personnel monitoring
- Sample according to approved SOPs, EM plans and GMP requirements
- Monitor cleanroom conditions during manufacturing to support aseptic processing
- Incubate samples, read plates, count colonies and identify microorganisms
- Review and trend EM data, and flag adverse trends early
- Investigate EM excursions and contribute to deviations, root cause analyses and CAPAs
- Report and escalate EM results on time
- Perform sterility, endotoxin and mycoplasma testing
- Perform QC testing of viral vectors and cell-based assays
- Write and review SOPs, EM programmes and quality documentation
- Act as a microbiology subject matter expert within the QC team
Required qualifications
- Master's degree or PhD in Microbiology or a related discipline
- At least 1 year of hands-on experience with cleanroom environmental monitoring
Solid knowledge of cleanroom behaviour and gowning procedures.
Hands-on experience with cell culture, cell-based assays and microbiological testing
Fluent professional English, written and spoken
Preferred qualifications
Experience working with a sterility isolator
Experience with molecular biology techniques
Experience with viral vector testing (AAV, lentivirus)
Experience from an ATMP or CDMO organisation
Who you are
You care about quality and pay close attention to detail, while staying flexible in a growing organisation. You take ownership, share what you know and like improving how things are done.
Why CCRM Nordic?
CCRM Nordic is on an exciting growth journey, and this is an opportunity to be part of building something truly unique. We offer a dynamic and collaborative environment where talented people come together to solve complex challenges and contribute to the advancement of cell and gene therapies.
Here, your expertise and ideas matter. You'll work alongside passionate colleagues, gain exposure to cutting-edge technologies, and have the opportunity to grow both professionally and personally while helping us shape the future of advanced therapy manufacturing.
Apply today!
Send in your application today. We review applications on an ongoing basis and look forward to hearing from you!
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