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ANALYTICAL LABORATORY TECHNICIAN

Info azienda.

With over 40 years of experience, Cerbios-Pharma SA is a Swiss-based private company with a global reach, specialized in the development and manufacturing of chemical, biotech, and biological active pharmaceutical ingredients (APIs).

In addition to a portfolio of generic APIs, Cerbios is a trusted CDMO partner for the production of highly potent APIs (HPAPIs) and antibody-drug conjugates (ADCs)—supporting clients from clinical development through to commercial manufacturing.

 

To enforce our R&D Analytical Validation and Services team, we are looking for a motivated and detail-oriented:.

 

                                                             Analytical Laboratory Technician

 

 

Competenze richieste.

  • University degree in Industrial Biotechnology or related, or else Chemistry or Pharmaceutical Sciences.
  • Academic or practical knowledge of analytical techniques for biotech products (e.g., mAbs, recombinant proteins, ADCs).
  • Basic knowledge of method development/validation principles consistent with ICH Q2(R2)/Q14.
  • Basic understanding of GMP.
  • Good command of English, both written and spoken.
  • A proactive mindset, strong team spirit, and a goal-oriented approach.
  • Excellent organizational and communication skills.
  • Solid problem-solving attitude.

Nice to have:

  • Familiarity with Quality by Design (QbD) concepts in analytical development.

  • Experience with statistical tools such as ANOVA, linear regression, statistical testing, and Design of Experiments (DoE).

     

Saranno richiesti i seguenti compiti.

  • Execute stability, IPCs and release analyses such as DAR, DAR distribution, conjugation heterogeneity, aggregates/charge variants, free drug/linker, process/residual impurities, ELISA.
  • Ensure full compliance with GMP standards and safety regulations.
  • Develop, optimize, qualify and validate fit-for-purpose analytical methods for ADCs (release, characterization, in-process control).
  • Operate LC-UV/FL/HR-MS; HIC/RP/SEC; CE-SDS/icIEF; ligand-binding/potency assays; author SOPs, protocols, and reports.
  • Execute practical activities related to: forced degradation, comparability studies, standard characterization.
  • Execute validations aligned to ICH Q2(R2)/Q14.
  • Collaborate with Process/Chemistry, Bioanalytics, and Quality; contribute input to regulatory sections.
  • Interface with client subject-matter experts. 
  • Execute work via our project-management system: scope, timeline, risk log, change control, and deliverable tracking.

Che cosa offriamo.

  • A meaningful role within a stable, innovation-driven organization operating globally.
  • An exciting opportunity to grow and broaden your ADC analytical expertise in a dynamic and specialized mid-size CDMO
  • Continuous professional training and development.
  • Competitive employment conditions, attractive benefits, and a healthy work-life balance

Tipologia di contratto

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