hirly
Sign inGet started free

Agcbio

GMP Manufacturing Technician, Downstream

Bresso, Italy

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Agcbio first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included
Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

See how it works

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Role family
Skilled trades
Seniority
Mid level
Country
IT
Work mode
On-site / unstated
First seen by hirly
7 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Attività Principali:

  • Purificazione di vettori virali con sistemi cromatografici e di ultrafiltrazione tangenziale seguendo le procedure operative standard e compilando la documentazione GMP, Batch record e moduli;
  • Allestimento delle attrezzature e dei materiali necessari alla lavorazione (preparazione kit disposable, impaccamento di colonne cromatografiche);
  • Preparazione in area GMP di soluzioni da impiegare nei processi di purificazione;
  • Esecuzione di piccoli interventi di manutenzione ordinaria e calibrazione periodica delle apparecchiature;
  • Lavorazioni sotto cappa a flusso laminare: prelievo di campionamenti, trasferimenti di fluidi, filtrazioni di soluzioni e bulk da purificare o purificati;
  • Redazione della documentazione correlata alle attività GMP Manufacturing: Batch Record, SOPs, protocolli e report;
  • Gestione della documentazione relativa a change e deviazioni.

Requisiti:

  • Laurea in Biotecnologie o similari
  • Disponibilità a lavorare nel weekend per specifiche esigenze lavorative

Salary range: 34000-35000 euro

  • Who We Are
  • AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in Italy. From our Milan site, we develop and manufacture life‑changing advanced biologics for some of the world’s most innovative pharmaceutical companies. Together with our team members across Europe, the U.S., and Japan, we deliver development and manufacturing of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells therapies. Across our global network, we are united by one mission: To work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.
Original posting on Agcbio's site ↗

Listed on hirly, a job board. hirly is not the employer: Agcbio is hiring for this role.

Similar jobs

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job