Quality Assurance Specialist

4 weken geleden

Tilburg, Noord-Brabant, Nederland Thermo Fisher Scientific Voltijd
Job Title: QC Technician

Job Summary:

We are seeking a highly skilled QC Technician to join our team at Thermo Fisher Scientific. As a QC Technician, you will be responsible for performing quality control tests on raw materials, in-process samples, and finished products to ensure compliance with established specifications and standards.

Key Responsibilities:
  • Perform quality control tests on raw materials, in-process samples, and finished products to ensure compliance with established specifications and standards.
  • Conduct routine analysis of samples using techniques such as HPLC, GC, FTIR, UV-Vis spectroscopy, and dissolution testing to obtain accurate results.
  • Analyze test results and data, and prepare accurate and detailed reports.
  • Investigate and resolve any deviations or discrepancies identified during testing, and communicate findings to relevant customers.
  • Support investigations into out-of-specification results and implement corrective and preventive actions as necessary.
  • Document all test results accurately and maintain detailed records in accordance with company procedures.
  • Collaborate with cross-functional teams including manufacturing, quality assurance, and regulatory affairs to support product release and compliance efforts.
  • Record and document experimental data, test results, observations, and any deviations from established procedures accurately and in a timely manner.
  • Assist in the calibration and maintenance of laboratory equipment to ensure accurate and reliable results.
  • 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.

About Us:

Diversity is important in creating an effective and challenging working environment. Integrity, Intensity, Innovation, and Involvement are key characteristics that we expect of all who is part of our community.

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