I

Incyte

Biopharmaceutical company pursuing drug discovery.

Technician Quality Control Physico Chemistry

Regulatory & Quality (Life Sciences)Updated on Nov 10
Full-timeYverdon-les-Bains, SwitzerlandNo salary listedIn-person

About the Job

Requirements

  • A CFC or higher degree in analytical chemistry or biochemistry is required.
  • At least five years of experience in a biotech, pharmaceutical, or chemical environment is required.
  • Hands-on experience in a Good Manufacturing Practice (GMP) environment and a Quality Control environment is required.
  • Knowledge of analytical method transfer and analytical method validation is required.
  • Knowledge of spectroscopic, HPLC, CE, and ELISA techniques is required.
  • Knowledge of Empower or SoftMax Pro is required.
  • Good writing skills are required.
  • Autonomy is required.
  • Native or fluent French is required.
  • Good knowledge of English is required.
  • Knowledge of common office software is required.
  • Weekend work may be required.

Responsibilities

  • Perform Quality Control analyses to support raw materials, production release, and stability plans for drug substance, including HPLC, UPLC, CGE, pH, FTIR, osmolality, protein concentration, ELISA tests, and appearance testing.
  • Review analytical data.
  • Act as a key user for Quality Control equipment software and method setup.
  • Perform basic laboratory work, including buffer preparation, waste disposal management, washing laboratory dishes, and cleaning laboratories.
  • Proactively propose problem resolutions.
  • Contribute to method technology transfer.
  • Author, review, and maintain Standard Operating Procedures, Work Instructions, and other Quality Control documents.
  • Support the selection, purchase, and commissioning of new equipment.
  • Support the management and supply of Quality Control consumables, reagents, and standards.
  • Support equipment maintenance and calibration and maintain relationships with suppliers.
  • Contribute to the efficient management of samples.
  • Raise, investigate, and close events, deviations, and non-conformances.
  • Act in accordance with compliance and legal requirements and company guidelines.
  • Contribute to a culture of business integrity and ethics.

About the Company

Incyte

Biopharmaceutical company pursuing drug discovery.

Incyte develops and sells medicines by discovering and developing new drugs, focusing on diseases in inflammation, autoimmunity, and blood cancers. Its core product, Jakafi (ruxolitinib), is a JAK1/2 inhibitor approved to treat a rare blood cancer and works by blocking JAK enzymes to reduce abnormal blood cell growth. The company also expands its pipeline through research collaborations, partnerships, and acquisitions, such as the 2024 purchase of Escient Pharmaceuticals to strengthen its inflammation and autoimmune portfolio. Unlike some competitors that rely mainly on internal programs, Incyte combines in-house discovery with external collaborations and strategic deals to grow its drug candidates from early research to approved therapies. The goal is to deliver medicines that help patients with serious diseases by building a diverse, clinically validated portfolio of treatments through internal efforts and partnerships.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Wilmington, DE
Founded
1991

Recently Posted Jobs

Explore more opportunities at Incyte

See more jobs