JOB DESCRIPTION

Our company is a global pharmaceutical company, part of the Softgel Business Unit, within Thermo Fisher Tilburg in the Netherlands. We develop and produce different pharmaceutical products as soft gel capsules for our own product portfolio and for customers.
Currently, we are seeking a skilled QC Technician to join our Quality Control Department. As a Quality Control Technician, you will play a pivotal role in ensuring that our products meet the highest quality standards and regulatory requirements. This position offers a great opportunity to collaborate in the development and manufacturing of life-saving pharmaceutical products.

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.
  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.

• Perform quality control tests on raw materials, in-process samples, and finished products to ensure compliance with established specifications and standards. Ensure compliance with regulatory requirements and Good Manufacturing Practices (GMP) in all quality control activities.
• 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.