QC Physico-Chemistry Technician – HPLC/ELISA Expert

Incyte Corporation; Lavamünd; Hybrid; EUR 45,000 - 65,000; Full time

Job summary

Incyte Corporation is seeking a QC Technician Physico Chemistry to perform QC analyses (HPLC, UPLC, CGE, ELISA, FTIR) and to support raw materials, production release, and stability testing. You will author procedures, participate in method transfer, and ensure quality control documentation.

The role requires a GMP background, experience with Empower or Soft Max PRO, and strong writing and teamwork abilities. Weekend work may be required, with on-site duties in a biotech setting.

Qualifications

• CFC or higher degree in analytical chemistry/biochemistry.
• At least 5 years’ experience in biotech/pharmaceutical/chemical environments.
• GMP and Quality Control experience.
• Knowledge of analytical method transfer and validation.
• Solid knowledge of spectroscopy, HPLC, CE and ELISA.
• Experience with Empower or Soft Max PRO.
• Good writing skills.
• Strong teamwork and autonomy.
• Weekend work may be required.

Responsibilities

• Performs QC analysis to support materials, production release and stability plans.
• Reviews analytical data.
• Acts as a key user for QC software and method setup.
• Performs basic lab work and waste management.
• Proposes problem resolutions and supports method transfer.
• Authors and maintains SOPs and lab documents.
• Supports equipment selection and commissioning.
• Supports supply of QC consumables and standards.
• Maintains equipment calibration and supplier relations.
• Contributes to sample management and deviation investigations.

Skills

HPLC

UPLC

CGE

ELISA

FTIR

Osmolality

Protein concentration

Analytical data review

Autonomy

Team spirit

Good writing skills

Education

CFC or higher degree in analytical chemistry/biochemistry

Tools

Empower

Soft Max PRO

Job description

Incyte Corporation is seeking a QC Technician Physico Chemistry to perform QC analyses (HPLC, UPLC, CGE, ELISA, FTIR) and to support raw materials, production release, and stability testing. You will author procedures, participate in method transfer, and ensure quality control documentation.

The role requires a GMP background, experience with Empower or Soft Max PRO, and strong writing and teamwork abilities. Weekend work may be required, with on-site duties in a biotech setting.