Vaccine Stability Analyst — Analytical Associate

LimmaTech Biologics AG

Schlieren

Remote

CHF 85,000 - 115,000

Full time

6 days ago
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Job summary

LimmaTech Biologics AG in Schlieren near Zürich is seeking an Analytical Associate (Stability Team) to support vaccine development through analytical method development and characterization of vaccine candidates.

The role focuses on stability/formulation studies, external CMOs coordination, and data/documentation across a multisite team in a GMP-like setting. English communication and hands-on lab work are essential.

Qualifications

  • Bachelor or master level in a chemistry/biochemistry/biology related field with lab experience.
  • Hands-on skills in immunoassays (ELISA) and analytical techniques (HPLC/biomolecule analysis).
  • Ability to work independently and in a multicultural team with good communication.

Responsibilities

  • Plan and perform stability, formulation, and compatibility studies.
  • Manage external stability studies at CMOs and coordinate timelines.
  • Review study results and prepare data for internal and external stakeholders.
  • Write and review SOPs, study plans, and analytical reports.
  • Analyze biomolecules (glyco-proteins, glyco-lipids, glycans) with state-of-the-art methods (HPLC, SDS-PAGE, Western blot, ELISA, DLS, FFF-MALS).
  • Support analytical method development for vaccine candidates produced via E. coli platforms.
  • Participate in knowledge transfers to CMOs and maintain lab safety standards.

Skills

Lab operations
Teamwork
Time management
English proficiency

Education

Laboratory technician qualification
BSc in Chemistry/Biochemistry/Biology
MSc in related discipline

Tools

HPLC
SDS-PAGE
Western blotting
ELISA
DLS
FFF-MALS

Job description

LimmaTech Biologics AG in Schlieren near Zürich is seeking an Analytical Associate (Stability Team) to support vaccine development through analytical method development and characterization of vaccine candidates.

The role focuses on stability/formulation studies, external CMOs coordination, and data/documentation across a multisite team in a GMP-like setting. English communication and hands-on lab work are essential.

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