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Technician QC Raw Materials & sampling

Job in Indiana, Indiana County, Pennsylvania, 15705, USA
Listing for: Incyte Corporation
Full Time position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector
Job Description & How to Apply Below
Location: Indiana

Overview

Job Summary (Primary function)

The QC Technician Raw Materials and sampling performs QC analysis to support sampling, testing and release of Raw Materials. The QC Technician Physico‑Chemistry also actively participates in new product introduction and method implementation. He/she also authors the analytical procedures and the general QC procedures.

Essential Functions of the Job (Key responsibilities)
  • Performs the sampling and the testing of Raw Materials
  • Performs analytical raw data review related to the sampling and testing of Raw Materials
  • Actively contributes to method implementation and equipment implementation.
  • Act as a key user for QC equipment software and method setup.
  • Performs basic laboratory work (buffer preparation, waste disposal management, washing of lab dishes, cleaning of the labs etc.).
  • Proactively propose problem resolutions
  • Efficiently contribute to method tech transfer.
  • Author, review and maintain Standard Operating Procedures, Work Instructions, and other quality control documents.
  • Supports selection, purchase and commissioning of new equipment.
  • Supports management supply of QC consumables, reagents and standards.
  • Supports maintenance/calibration of equipment and keeps relationship with suppliers.
  • Contribute to the efficient management of samples.
  • Proactively propose problem resolutions.
  • Raise, investigate and close events, deviations and non-conformances.
  • Contribute positively to a strong culture of business integrity and ethics.
  • Act within compliance and legal requirements as well as within company guidelines.
Qualifications (Minimal acceptable level of education, work experience, and competency)
  • CFC or higher degree in analytical chemistry/biochemistry
  • At least 5 years’ experience in the biotech, pharmaceutical or chemical environment
  • Hands‑on experience in a GMP environment and a Quality Control environment.
  • Good knowledge of analytical method transfer and analytical method validation.
  • Solid knowledge in spectroscopic techniques.
  • Good writing skills.
  • Excellent team spirit.
  • Autonomy
  • French:
    Native or Fluent
  • English:
    Basic knowledge
  • Knowledge of most common office software.
  • Work the weekend may be required.
Disclaimer

The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

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