Chemical Analist - Method Development & Validation

As a method developer in the QC lab in Venray, you are tasked with developing a new method. This challenge is tailor-made for you. You will develop an analytical method that can accurately measure the concentration of the API. Your goal is to create a method that is precise, sensitive, robust, and consistent. This project is in good hands with you.

The next step is conducting a literature review. With the defined assignment in mind, you perform thorough research. You search for and identify existing methods that have been successfully used before by consulting scientific databases and pharmacopoeias. This allows you to compile a shortlist of potential methods that can be adapted and tested.

You enter the lab to take the next step: testing and optimizing the methods. After countless experiments and refinements, you develop a method that meets all the requirements of sensitivity, accuracy, and robustness.

Next comes validation, where you rigorously test the method for specificity, linearity, and robustness. Each test confirms that your method is not only consistent and reliable but also capable of accurately measuring even the smallest concentrations of the API and degradation products. With the validation successfully completed, you implement the method in the QC lab. The team is trained, and the SOPs are updated, ensuring that the method is ready for routine analysis. You look back with satisfaction on a project that, thanks to your expertise and dedication, not only contributes to the quality of our products but also to the safety of animals worldwide treated with Interchemie’s high-quality products.

Your experience in chemical analysis and method development is supported by solid theoretical knowledge. Experience with HPLC is an absolute must for this position. You will be part of a team where we work independently, but teamwork is highly valued. We are hardworking, rational individuals with both feet on the ground.

Responsibilities

• Performing Method Development and Validation: You carry out tasks related to method development and validation within the QC laboratory, following GMP and GMP+ quality systems.
• Conducting Literature Research: You conduct thorough literature research to identify and improve new and existing analytical methods, integrating the latest scientific developments into your work.
• Writing Procedures and Reports: You are responsible for drafting procedures and reports in line with GMP and/or GMP+ guidelines.
• Initiating Improvement Proposals and Root Cause Analyses: You show initiative by making improvement proposals and are involved in conducting root cause analyses to ensure continuous improvement.
• Collaborating with Various Departments: Your knowledge and personality allow you to work closely with various departments within the organization to achieve quality goals.