
QC Technician
- Tilburg, Noord-Brabant
- Vast
- Voltijds
- 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.
- 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.