Quality Assurance Specialist

4 uur geleden

Tilburg, Noord-Brabant, Nederland Thermo Fisher Scientific Voltijd
Job Summary

As a Quality Assurance Specialist at Thermo Fisher Scientific, you will play a critical role in ensuring the quality and compliance of our pharmaceutical products. Your primary responsibility will be to perform quality control tests on raw materials, in-process samples, and finished products to ensure compliance with established specifications and standards. You will also be responsible for conducting routine analysis of samples using techniques such as HPLC, GC, FTIR, UV-Vis spectroscopy, and dissolution testing to obtain accurate results. Additionally, you will analyze test results and data, and prepare accurate and detailed reports. You will investigate and resolve any deviations or discrepancies identified during testing, and communicate findings to relevant customers. You will also support investigations into out-of-specification results and implement corrective and preventive actions as necessary. Furthermore, you will document all test results accurately and maintain detailed records in accordance with company procedures. You will collaborate with cross-functional teams including manufacturing, quality assurance, and regulatory affairs to support product release and compliance efforts. You will record and document experimental data, test results, observations, and any deviations from established procedures accurately and in a timely manner. You will also assist in the calibration and maintenance of laboratory equipment to ensure accurate and reliable results. You will contribute to continuous improvement initiatives within the quality control department.

Qualifications:

  • MBO or Bachelor's degree in Chemistry, or a related field
  • Previous experience as a Quality Control Technician in the pharmaceutical industry is preferred.
  • Proficiency in using laboratory equipment and analytical instruments.
  • Strong knowledge of quality control principles, techniques, and regulations, including cGMP guidelines.
  • Good analytical and problem-solving skills to troubleshoot basic laboratory issues.
  • Strong organizational and time management skills to meet timelines and prioritize tasks effectively.
  • Effective communication skills, both verbal and written, with the ability to collaborate across departments.
  • Ability to work independently and in a team-oriented environment.
  • Flexibility to work in a fast-paced and dynamic pharmaceutical manufacturing environment.
  • Commitment to maintaining a safe and compliant laboratory environment.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) for data entry and report generation.

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